Introduction
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Source: https://github.com/AllenNeuralDynamics/ComputationalReviewPV/blob/df9fc7e8d455b084152c9d713558dae0013cef21/content/01_introduction.md
Citation anchors captured: 45
Citation contexts
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1CitationAmong 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 1CitationAmong 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...
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2CitationAmong 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 1CitationAmong 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...
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3CitationAmong 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 1CitationAmong 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...
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4CitationAmong 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 1CitationAmong 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...
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5CitationAmong 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 1CitationAmong 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...
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1CitationAmong 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 1CitationAmong 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...
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1CitationAmong 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 1CitationAmong 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...
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1CitationAmong 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 1CitationAmong 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...
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1CitationAmong 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 1CitationAmong 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...
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1CitationAmong 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 1CitationAmong 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...
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2CitationAmong 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...
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2CitationAmong 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...
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2CitationAmong 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-identityexamines 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... -
2CitationAmong 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-identityexamines 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... -
2CitationAmong 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-identityexamines 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... -
2CitationAmong 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-identityexamines 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... -
2CitationAmong 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-identityexamines 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... -
2CitationAmong 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-identityexamines 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... -
2CitationAmong 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-identityexamines 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... -
2CitationAmong 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-identityexamines 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... -
1CitationAmong 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-identityexamines 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... -
1CitationAmong 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-physiologyanalyzes 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... -
1CitationAmong 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-physiologyanalyzes 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... -
1CitationAmong 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-physiologyanalyzes 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... -
1CitationAmong 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-physiologyanalyzes 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... -
1CitationAmong 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-physiologyanalyzes 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... -
1CitationAmong 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-physiologyanalyzes 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... -
1CitationAmong 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-physiologyanalyzes 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... -
1CitationAmong 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-physiologyanalyzes 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... -
1CitationAmong 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-physiologyanalyzes 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... -
3CitationAmong 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-physiologyanalyzes 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... -
3CitationAmong 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-physiologyanalyzes 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... -
3CitationAmong 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-diseaseevaluates 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... -
3CitationAmong 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-diseaseevaluates 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... -
3CitationAmong 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-diseaseevaluates 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... -
3CitationAmong 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-diseaseevaluates 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... -
3CitationAmong 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-diseaseevaluates 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... -
3CitationAmong 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 3CitationAmong 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...
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3CitationAmong 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 1CitationAmong 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...
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1CitationAmong 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 1CitationAmong 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...
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1CitationAmong 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 1CitationAmong 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...
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1CitationAmong 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 1CitationAmong 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.
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1CitationAmong 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 1CitationAmong 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.
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1CitationAmong 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...
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4CitationAmong 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
- [Tremblay2016gabaergic] “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...”
- [Pelkey2017hippocampal] “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...”
- [Hu2017cortical] “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...”
- [Buzsaki2012mechanisms] “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...”
- [Lewis2012cortical] “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...”
- [Ogiwara2007nav] “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...”
- [Verret2012inhibitory] “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...”
- [Selten2018inhibitory] “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...”
- [Huang2019diversity] “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...”
- [Bartholome2020composite] “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...”
- [Yao2021taxonomy] “**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...”
- [Scala2021phenotypic] “**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...”
- [Gouwens2020integrated] “**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...”
- [Fishell2020interneuron] “**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...”
- [BecerraHernandez2026cortical] “**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...”
- [Rozov2024dialectics] “**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...”
- [Kawaguchi1993physiological] “**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...”
- [Okaty2009transcriptional] “**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...”
- [Bartos2002fast] “**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...”
- [Woodruff2009depolarizing] “**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...”
- [Fekete2025synaptic] “**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...”
- [Isaacson2011inhibition] “**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...”
- [Znamenskiy2024functional] “**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...”
- [Atallah2012parvalbumin] “**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...”
- [Pakan2016behavioral] “**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...”
- [Klausberger2008neuronal] “**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...”
- [Caroni2015inhibitory] “**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...”
- [Sohal2009parvalbumin] “**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...”
- [Cardin2009driving] “**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...”
- [Nakazawa2012gabaergic] “**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...”
- [Wang2010neurophysiological] “**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...”
- [Sadeh2017assessing] “**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...”
- [Yuste2020community] “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...”
- [Morishima2017segregated] “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...”
- [Bakken2021comparative] “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.”
- [Kaar2019pre] “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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