Introduction

computational_review_section · SciDEX wiki

Introduction

This section is represented as a source-backed SciDEX wiki artifact. The full source remains in the original computational-review repository.

Source: https://github.com/AllenNeuralDynamics/ComputationalReviewPV/blob/df9fc7e8d455b084152c9d713558dae0013cef21/content/01_introduction.md

Citation anchors captured: 45

Citation contexts

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference, PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...

  • 2Citationpaper:paper-ad1611a9283aAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference, PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...

  • 3Citationpaper:paper-19bf293de901Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference, PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...

  • 4Citationpaper:paper-48b808525190Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference, PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...

  • 5Citationpaper:paper-6d36973b50abAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference, PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference0 Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference1, PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference2 Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference3, PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference4 Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference5, PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference6 Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference7, PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference8 Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference9, PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...

  • 2Citationpaper:paper-ad1611a9283aAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference0 The sheer volume of research spanning molecular biology, developmental neuroscience, electrophysiology, circuit analysis, systems neuroscience, computational modeling, and translational medicine has generated a literature so vast that no single investigator can hold its full scope in view. More than a thousand publications per year now mention PV interneurons, and the rate continues to accelerate. This breadth prese...

  • 2Citationpaper:paper-ad1611a9283aAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference1 The sheer volume of research spanning molecular biology, developmental neuroscience, electrophysiology, circuit analysis, systems neuroscience, computational modeling, and translational medicine has generated a literature so vast that no single investigator can hold its full scope in view. More than a thousand publications per year now mention PV interneurons, and the rate continues to accelerate. This breadth prese...

  • 2Citationpaper:paper-ad1611a9283aAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference2 Act I — Identity: What PV interneurons ARE. The review begins by establishing PV interneuron identity at four complementary levels. {ref}sec-molecular-identity examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...

  • 2Citationpaper:paper-ad1611a9283aAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference3 Act I — Identity: What PV interneurons ARE. The review begins by establishing PV interneuron identity at four complementary levels. {ref}sec-molecular-identity examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...

  • 2Citationpaper:paper-ad1611a9283aAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference4 Act I — Identity: What PV interneurons ARE. The review begins by establishing PV interneuron identity at four complementary levels. {ref}sec-molecular-identity examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...

  • 2Citationpaper:paper-ad1611a9283aAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference5 Act I — Identity: What PV interneurons ARE. The review begins by establishing PV interneuron identity at four complementary levels. {ref}sec-molecular-identity examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...

  • 2Citationpaper:paper-ad1611a9283aAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference6 Act I — Identity: What PV interneurons ARE. The review begins by establishing PV interneuron identity at four complementary levels. {ref}sec-molecular-identity examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...

  • 2Citationpaper:paper-ad1611a9283aAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference7 Act I — Identity: What PV interneurons ARE. The review begins by establishing PV interneuron identity at four complementary levels. {ref}sec-molecular-identity examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...

  • 2Citationpaper:paper-ad1611a9283aAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference8 Act I — Identity: What PV interneurons ARE. The review begins by establishing PV interneuron identity at four complementary levels. {ref}sec-molecular-identity examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...

  • 2Citationpaper:paper-ad1611a9283aAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference9 Act I — Identity: What PV interneurons ARE. The review begins by establishing PV interneuron identity at four complementary levels. {ref}sec-molecular-identity examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference0 Act I — Identity: What PV interneurons ARE. The review begins by establishing PV interneuron identity at four complementary levels. {ref}sec-molecular-identity examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference1 Act II — Mechanism: What PV interneurons DO. Having established identity, the review turns to function. {ref}sec-synaptic-physiology analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference2 Act II — Mechanism: What PV interneurons DO. Having established identity, the review turns to function. {ref}sec-synaptic-physiology analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference3 Act II — Mechanism: What PV interneurons DO. Having established identity, the review turns to function. {ref}sec-synaptic-physiology analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference4 Act II — Mechanism: What PV interneurons DO. Having established identity, the review turns to function. {ref}sec-synaptic-physiology analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference5 Act II — Mechanism: What PV interneurons DO. Having established identity, the review turns to function. {ref}sec-synaptic-physiology analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference6 Act II — Mechanism: What PV interneurons DO. Having established identity, the review turns to function. {ref}sec-synaptic-physiology analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference7 Act II — Mechanism: What PV interneurons DO. Having established identity, the review turns to function. {ref}sec-synaptic-physiology analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference8 Act II — Mechanism: What PV interneurons DO. Having established identity, the review turns to function. {ref}sec-synaptic-physiology analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference9 Act II — Mechanism: What PV interneurons DO. Having established identity, the review turns to function. {ref}sec-synaptic-physiology analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...

  • 3Citationpaper:paper-19bf293de901Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference0 Act II — Mechanism: What PV interneurons DO. Having established identity, the review turns to function. {ref}sec-synaptic-physiology analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...

  • 3Citationpaper:paper-19bf293de901Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference1 Act II — Mechanism: What PV interneurons DO. Having established identity, the review turns to function. {ref}sec-synaptic-physiology analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...

  • 3Citationpaper:paper-19bf293de901Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference2 Act III — Translation and Synthesis: What it all MEANS. The final act extends PV biology across species and into disease. {ref}sec-species-disease evaluates the clinical relevance of PV dysfunction in schizophrenia, epilepsy, autism, and Alzheimer’s disease, with explicit attention to replication status and the species-specific considerations that constrain translation [Lewis2012cortical, Ogiwara2007nav, Nakaz...

  • 3Citationpaper:paper-19bf293de901Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference3 Act III — Translation and Synthesis: What it all MEANS. The final act extends PV biology across species and into disease. {ref}sec-species-disease evaluates the clinical relevance of PV dysfunction in schizophrenia, epilepsy, autism, and Alzheimer’s disease, with explicit attention to replication status and the species-specific considerations that constrain translation [Lewis2012cortical, Ogiwara2007nav, Nakaz...

  • 3Citationpaper:paper-19bf293de901Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference4 Act III — Translation and Synthesis: What it all MEANS. The final act extends PV biology across species and into disease. {ref}sec-species-disease evaluates the clinical relevance of PV dysfunction in schizophrenia, epilepsy, autism, and Alzheimer’s disease, with explicit attention to replication status and the species-specific considerations that constrain translation [Lewis2012cortical, Ogiwara2007nav, Nakaz...

  • 3Citationpaper:paper-19bf293de901Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference5 Act III — Translation and Synthesis: What it all MEANS. The final act extends PV biology across species and into disease. {ref}sec-species-disease evaluates the clinical relevance of PV dysfunction in schizophrenia, epilepsy, autism, and Alzheimer’s disease, with explicit attention to replication status and the species-specific considerations that constrain translation [Lewis2012cortical, Ogiwara2007nav, Nakaz...

  • 3Citationpaper:paper-19bf293de901Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference6 Act III — Translation and Synthesis: What it all MEANS. The final act extends PV biology across species and into disease. {ref}sec-species-disease evaluates the clinical relevance of PV dysfunction in schizophrenia, epilepsy, autism, and Alzheimer’s disease, with explicit attention to replication status and the species-specific considerations that constrain translation [Lewis2012cortical, Ogiwara2007nav, Nakaz...

  • 3Citationpaper:paper-19bf293de901Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference7 Several cross-cutting tensions recur throughout the review, serving as organizing threads that connect otherwise disparate levels of analysis. The first is discrete versus continuous classification: whether PV interneurons subdivide into cleanly separable types or occupy a continuum that resists categorical boundaries 3Citationpaper:paper-19bf293de901Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference8. This question arises at every level — molecular ta...

  • 3Citationpaper:paper-19bf293de901Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference9 Several cross-cutting tensions recur throughout the review, serving as organizing threads that connect otherwise disparate levels of analysis. The first is discrete versus continuous classification: whether PV interneurons subdivide into cleanly separable types or occupy a continuum that resists categorical boundaries 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference0. This question arises at every level — molecular ta...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference1 The second is the specificity question: whether PV inhibition is a blunt instrument applied uniformly to local circuits or a precisely tuned signal shaped by connection-specific rules 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference2. This debate manifests in the blanket-versus-selective inhibition controversy, in the question of whether PV tuning is feature-specific or co-tuned with locomotion and arousal, an...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference3 The second is the specificity question: whether PV inhibition is a blunt instrument applied uniformly to local circuits or a precisely tuned signal shaped by connection-specific rules 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference4. This debate manifests in the blanket-versus-selective inhibition controversy, in the question of whether PV tuning is feature-specific or co-tuned with locomotion and arousal, an...

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference5 The third is the translation gap: the distance between mouse models and human disease, between in vitro preparations and in vivo function, and between computational predictions and experimental testability 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference6. This gap constrains every therapeutic claim derived from PV interneuron research and demands explicit acknowledgment throughout.

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference7 The third is the translation gap: the distance between mouse models and human disease, between in vitro preparations and in vivo function, and between computational predictions and experimental testability 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference8. This gap constrains every therapeutic claim derived from PV interneuron research and demands explicit acknowledgment throughout.

  • 1Citationpaper:paper-53c8505de50fAmong the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference9 The fourth is methodological constraint: the extent to which our conclusions about PV biology are shaped — and potentially distorted — by the tools used to study these cells. Cre-line specificity and off-target recombination, optogenetic activation artifacts, slice preparation effects on chloride reversal potentials, the conflation of correlation with causation in loss-of-function studies, and the limited cell-t...

  • 4Citationpaper:paper-48b808525190Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...content/01_introduction.md:line 6Open reference0 The fourth is methodological constraint: the extent to which our conclusions about PV biology are shaped — and potentially distorted — by the tools used to study these cells. Cre-line specificity and off-target recombination, optogenetic activation artifacts, slice preparation effects on chloride reversal potentials, the conflation of correlation with causation in loss-of-function studies, and the limited cell-t...

References

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  2. [Pelkey2017hippocampal] paper:paper-ad1611a9283a “Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...”
  3. [Hu2017cortical] paper:paper-19bf293de901 “Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...”
  4. [Buzsaki2012mechanisms] paper:paper-48b808525190 “Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...”
  5. [Lewis2012cortical] paper:paper-6d36973b50ab “Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...”
  6. [Ogiwara2007nav] paper:paper-fd8f15e7c2e1 “Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...”
  7. [Verret2012inhibitory] paper:paper-4cb1cf98f0c1 “Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...”
  8. [Selten2018inhibitory] paper:paper-5404be9f8464 “Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...”
  9. [Huang2019diversity] paper:paper-560189f9d2b5 “Among the diverse cell types that compose the mammalian cerebral cortex, few have attracted as much sustained attention as parvalbumin-expressing (PV+) interneurons. Constituting approximately 40% of cortical GABAergic neurons [Tremblay2016gabaergic], PV interneurons occupy a unique position in neural circuit architecture: they are the principal source of perisomatic inhibition onto pyramidal cells, the fastest-firi...”
  10. [Bartholome2020composite] paper:paper-aaf84aa85982 “The sheer volume of research spanning molecular biology, developmental neuroscience, electrophysiology, circuit analysis, systems neuroscience, computational modeling, and translational medicine has generated a literature so vast that no single investigator can hold its full scope in view. More than a thousand publications per year now mention PV interneurons, and the rate continues to accelerate. This breadth prese...”
  11. [Yao2021taxonomy] paper:paper-4dfe44516146 “**Act I — Identity: What PV interneurons ARE.** The review begins by establishing PV interneuron identity at four complementary levels. {ref}`sec-molecular-identity` examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...”
  12. [Scala2021phenotypic] paper:paper-be132b319290 “**Act I — Identity: What PV interneurons ARE.** The review begins by establishing PV interneuron identity at four complementary levels. {ref}`sec-molecular-identity` examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...”
  13. [Gouwens2020integrated] paper:paper-pm-33186530 “**Act I — Identity: What PV interneurons ARE.** The review begins by establishing PV interneuron identity at four complementary levels. {ref}`sec-molecular-identity` examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...”
  14. [Fishell2020interneuron] paper:paper-23eff3bbd875 “**Act I — Identity: What PV interneurons ARE.** The review begins by establishing PV interneuron identity at four complementary levels. {ref}`sec-molecular-identity` examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...”
  15. [BecerraHernandez2026cortical] paper:paper-b0544e9fbfc3 “**Act I — Identity: What PV interneurons ARE.** The review begins by establishing PV interneuron identity at four complementary levels. {ref}`sec-molecular-identity` examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...”
  16. [Rozov2024dialectics] paper:paper-21b4420ef885 “**Act I — Identity: What PV interneurons ARE.** The review begins by establishing PV interneuron identity at four complementary levels. {ref}`sec-molecular-identity` examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...”
  17. [Kawaguchi1993physiological] paper:paper-3522fd039446 “**Act I — Identity: What PV interneurons ARE.** The review begins by establishing PV interneuron identity at four complementary levels. {ref}`sec-molecular-identity` examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...”
  18. [Okaty2009transcriptional] paper:paper-591943f1ad14 “**Act I — Identity: What PV interneurons ARE.** The review begins by establishing PV interneuron identity at four complementary levels. {ref}`sec-molecular-identity` examines the transcriptomic taxonomy, revealing that PV interneurons form a coherent molecular subclass defined by co-expression of parvalbumin with Kv3 potassium channels, Nav1.1 sodium channels, and ErbB4, yet harbor internal diversity that recent sin...”
  19. [Bartos2002fast] paper:paper-a9bffd9b9fbb “**Act II — Mechanism: What PV interneurons DO.** Having established identity, the review turns to function. {ref}`sec-synaptic-physiology` analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...”
  20. [Woodruff2009depolarizing] paper:paper-c803cdbd5cbd “**Act II — Mechanism: What PV interneurons DO.** Having established identity, the review turns to function. {ref}`sec-synaptic-physiology` analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...”
  21. [Fekete2025synaptic] paper:paper-4d0daef43dfa “**Act II — Mechanism: What PV interneurons DO.** Having established identity, the review turns to function. {ref}`sec-synaptic-physiology` analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...”
  22. [Isaacson2011inhibition] paper:paper-a8a1c6d6bbad “**Act II — Mechanism: What PV interneurons DO.** Having established identity, the review turns to function. {ref}`sec-synaptic-physiology` analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...”
  23. [Znamenskiy2024functional] paper:paper-7ab8027f125a “**Act II — Mechanism: What PV interneurons DO.** Having established identity, the review turns to function. {ref}`sec-synaptic-physiology` analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...”
  24. [Atallah2012parvalbumin] paper:paper-6c403fbadc9b “**Act II — Mechanism: What PV interneurons DO.** Having established identity, the review turns to function. {ref}`sec-synaptic-physiology` analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...”
  25. [Pakan2016behavioral] paper:paper-acf576c0a2ed “**Act II — Mechanism: What PV interneurons DO.** Having established identity, the review turns to function. {ref}`sec-synaptic-physiology` analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...”
  26. [Klausberger2008neuronal] paper:paper-f5e82131eb03 “**Act II — Mechanism: What PV interneurons DO.** Having established identity, the review turns to function. {ref}`sec-synaptic-physiology` analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...”
  27. [Caroni2015inhibitory] paper:paper-a15d5b81f78a “**Act II — Mechanism: What PV interneurons DO.** Having established identity, the review turns to function. {ref}`sec-synaptic-physiology` analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...”
  28. [Sohal2009parvalbumin] paper:paper-d5a7d63abc9a “**Act II — Mechanism: What PV interneurons DO.** Having established identity, the review turns to function. {ref}`sec-synaptic-physiology` analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...”
  29. [Cardin2009driving] paper:3767f6c5-663b-42ad-bf68-d37f6f00b49d “**Act II — Mechanism: What PV interneurons DO.** Having established identity, the review turns to function. {ref}`sec-synaptic-physiology` analyzes synaptic input specificity, output targeting, short-term depression dynamics, long-term plasticity, gap-junction coupling, and neuromodulatory regulation, including the long-contested polarity of chandelier cell synapses at the axon initial segment [Bartos2002fast, Woodr...”
  30. [Nakazawa2012gabaergic] paper:paper-faa24c65b3dd “**Act III — Translation and Synthesis: What it all MEANS.** The final act extends PV biology across species and into disease. {ref}`sec-species-disease` evaluates the clinical relevance of PV dysfunction in schizophrenia, epilepsy, autism, and Alzheimer's disease, with explicit attention to replication status and the species-specific considerations that constrain translation [Lewis2012cortical, Ogiwara2007nav, Nakaz...”
  31. [Wang2010neurophysiological] paper:paper-b8f4cf874563 “**Act III — Translation and Synthesis: What it all MEANS.** The final act extends PV biology across species and into disease. {ref}`sec-species-disease` evaluates the clinical relevance of PV dysfunction in schizophrenia, epilepsy, autism, and Alzheimer's disease, with explicit attention to replication status and the species-specific considerations that constrain translation [Lewis2012cortical, Ogiwara2007nav, Nakaz...”
  32. [Sadeh2017assessing] paper:paper-5135d667ceac “**Act III — Translation and Synthesis: What it all MEANS.** The final act extends PV biology across species and into disease. {ref}`sec-species-disease` evaluates the clinical relevance of PV dysfunction in schizophrenia, epilepsy, autism, and Alzheimer's disease, with explicit attention to replication status and the species-specific considerations that constrain translation [Lewis2012cortical, Ogiwara2007nav, Nakaz...”
  33. [Yuste2020community] paper:paper-pm-32839617 “Several cross-cutting tensions recur throughout the review, serving as organizing threads that connect otherwise disparate levels of analysis. The first is **discrete versus continuous classification**: whether PV interneurons subdivide into cleanly separable types or occupy a continuum that resists categorical boundaries [Gouwens2020integrated, Yuste2020community]. This question arises at every level — molecular ta...”
  34. [Morishima2017segregated] paper:paper-aa18bb0de98d “The second is **the specificity question**: whether PV inhibition is a blunt instrument applied uniformly to local circuits or a precisely tuned signal shaped by connection-specific rules [Znamenskiy2024functional, Morishima2017segregated]. This debate manifests in the blanket-versus-selective inhibition controversy, in the question of whether PV tuning is feature-specific or co-tuned with locomotion and arousal, an...”
  35. [Bakken2021comparative] paper:paper-pm-34616062 “The third is **the translation gap**: the distance between mouse models and human disease, between in vitro preparations and in vivo function, and between computational predictions and experimental testability [Bakken2021comparative, Kaar2019pre]. This gap constrains every therapeutic claim derived from PV interneuron research and demands explicit acknowledgment throughout.”
  36. [Kaar2019pre] paper:paper-8a23937e9dab “The third is **the translation gap**: the distance between mouse models and human disease, between in vitro preparations and in vivo function, and between computational predictions and experimental testability [Bakken2021comparative, Kaar2019pre]. This gap constrains every therapeutic claim derived from PV interneuron research and demands explicit acknowledgment throughout.”

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