K+ Channel Expression Distinguishes Subpopulations of Parvalbumin- and Somatostatin-Containing Neocortical Interneurons
Kv3.1 and Kv3.2 K(+) channel proteins form similar voltage-gated K(+) channels with unusual properties, including fast activation at voltages positive to -10 mV and very fast deactivation rates. These properties are thought to facilitate sustained high-frequency firing. Kv3.1 subunits are specifical...
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creator | Chow, A Erisir, A Farb, C Nadal, M. S Ozaita, A Lau, D Welker, E Rudy, B |
description | Kv3.1 and Kv3.2 K(+) channel proteins form similar voltage-gated K(+) channels with unusual properties, including fast activation at voltages positive to -10 mV and very fast deactivation rates. These properties are thought to facilitate sustained high-frequency firing. Kv3.1 subunits are specifically found in fast-spiking, parvalbumin (PV)-containing cortical interneurons, and recent studies have provided support for a crucial role in the generation of the fast-spiking phenotype. Kv3.2 mRNAs are also found in a small subset of neocortical neurons, although the distribution of these neurons is different. We raised antibodies directed against Kv3.2 proteins and used dual-labeling methods to identify the neocortical neurons expressing Kv3.2 proteins and to determine their subcellular localization. Kv3.2 proteins are prominently expressed in patches in somatic and proximal dendritic membrane as well as in axons and presynaptic terminals of GABAergic interneurons. Kv3.2 subunits are found in all PV-containing neurons in deep cortical layers where they probably form heteromultimeric channels with Kv3.1 subunits. In contrast, in superficial layer PV-positive neurons Kv3.2 immunoreactivity is low, but Kv3.1 is still prominently expressed. Because Kv3.1 and Kv3.2 channels are differentially modulated by protein kinases, these results raise the possibility that the fast-spiking properties of superficial- and deep-layer PV neurons are differentially regulated by neuromodulators. Interestingly, Kv3. 2 but not Kv3.1 proteins are also prominent in a subset of seemingly non-fast-spiking, somatostatin- and calbindin-containing interneurons, suggesting that the Kv3.1-Kv3.2 current type can have functions other than facilitating high-frequency firing. |
doi_str_mv | 10.1523/jneurosci.19-21-09332.1999 |
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S ; Ozaita, A ; Lau, D ; Welker, E ; Rudy, B</creator><creatorcontrib>Chow, A ; Erisir, A ; Farb, C ; Nadal, M. S ; Ozaita, A ; Lau, D ; Welker, E ; Rudy, B</creatorcontrib><description>Kv3.1 and Kv3.2 K(+) channel proteins form similar voltage-gated K(+) channels with unusual properties, including fast activation at voltages positive to -10 mV and very fast deactivation rates. These properties are thought to facilitate sustained high-frequency firing. Kv3.1 subunits are specifically found in fast-spiking, parvalbumin (PV)-containing cortical interneurons, and recent studies have provided support for a crucial role in the generation of the fast-spiking phenotype. Kv3.2 mRNAs are also found in a small subset of neocortical neurons, although the distribution of these neurons is different. We raised antibodies directed against Kv3.2 proteins and used dual-labeling methods to identify the neocortical neurons expressing Kv3.2 proteins and to determine their subcellular localization. Kv3.2 proteins are prominently expressed in patches in somatic and proximal dendritic membrane as well as in axons and presynaptic terminals of GABAergic interneurons. Kv3.2 subunits are found in all PV-containing neurons in deep cortical layers where they probably form heteromultimeric channels with Kv3.1 subunits. In contrast, in superficial layer PV-positive neurons Kv3.2 immunoreactivity is low, but Kv3.1 is still prominently expressed. Because Kv3.1 and Kv3.2 channels are differentially modulated by protein kinases, these results raise the possibility that the fast-spiking properties of superficial- and deep-layer PV neurons are differentially regulated by neuromodulators. Interestingly, Kv3. 2 but not Kv3.1 proteins are also prominent in a subset of seemingly non-fast-spiking, somatostatin- and calbindin-containing interneurons, suggesting that the Kv3.1-Kv3.2 current type can have functions other than facilitating high-frequency firing.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/jneurosci.19-21-09332.1999</identifier><identifier>PMID: 10531438</identifier><language>eng</language><publisher>United States: Soc Neuroscience</publisher><subject>Amino Acid Sequence ; Animals ; Antibodies ; Axons - physiology ; Axons - ultrastructure ; Brain - physiology ; Cell Line ; Cell Membrane - physiology ; Cell Membrane - ultrastructure ; Dendrites - physiology ; Dendrites - ultrastructure ; Fast spiking ; Fisiologia ; GABA ; High-frequency firing ; Humans ; Inhibition ; Interneurons - cytology ; Interneurons - physiology ; Kv3 subunits ; Mice ; Molecular Sequence Data ; Neocortex - cytology ; Neocortex - physiology ; Neurones ; Neurons - classification ; Neurons - cytology ; Neurons - physiology ; Neuropeptides - analysis ; Neuropeptides - genetics ; Neuropeptides - physiology ; Parvalbumins - analysis ; Peptide Fragments - chemistry ; Peptide Fragments - immunology ; Potassium Channels - analysis ; Potassium Channels - genetics ; Potassium Channels - physiology ; Potassium Channels, Voltage-Gated ; Rabbits ; Rats ; Recombinant Proteins - analysis ; Recombinant Proteins - metabolism ; Shaw Potassium Channels ; Somatosensory Cortex - cytology ; Somatosensory Cortex - physiology ; Somatostatin - analysis ; Transfection ; Voltage-gated K1 channels ; Xarxes neuronals (Neurobiologia)</subject><ispartof>The Journal of neuroscience, 1999-11, Vol.19 (21), p.9332-9345</ispartof><rights>info:eu-repo/semantics/openAccess (c) 1999, Society for Neuroscience. The published version is available at: <a href="http://www.jneurosci.org/content/19/21/9332">http://www.jneurosci.org/content/19/21/9332</a></rights><rights>Copyright © 1999 Society for Neuroscience 1999</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c619t-bce41afb3619b773cd09548b3a786f9ab588a1dc2e8c95c5068fecad4e9e73ca3</citedby><cites>FETCH-LOGICAL-c619t-bce41afb3619b773cd09548b3a786f9ab588a1dc2e8c95c5068fecad4e9e73ca3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6782929/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6782929/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,26953,27903,27904,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10531438$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chow, A</creatorcontrib><creatorcontrib>Erisir, A</creatorcontrib><creatorcontrib>Farb, C</creatorcontrib><creatorcontrib>Nadal, M. S</creatorcontrib><creatorcontrib>Ozaita, A</creatorcontrib><creatorcontrib>Lau, D</creatorcontrib><creatorcontrib>Welker, E</creatorcontrib><creatorcontrib>Rudy, B</creatorcontrib><title>K+ Channel Expression Distinguishes Subpopulations of Parvalbumin- and Somatostatin-Containing Neocortical Interneurons</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>Kv3.1 and Kv3.2 K(+) channel proteins form similar voltage-gated K(+) channels with unusual properties, including fast activation at voltages positive to -10 mV and very fast deactivation rates. These properties are thought to facilitate sustained high-frequency firing. Kv3.1 subunits are specifically found in fast-spiking, parvalbumin (PV)-containing cortical interneurons, and recent studies have provided support for a crucial role in the generation of the fast-spiking phenotype. Kv3.2 mRNAs are also found in a small subset of neocortical neurons, although the distribution of these neurons is different. We raised antibodies directed against Kv3.2 proteins and used dual-labeling methods to identify the neocortical neurons expressing Kv3.2 proteins and to determine their subcellular localization. Kv3.2 proteins are prominently expressed in patches in somatic and proximal dendritic membrane as well as in axons and presynaptic terminals of GABAergic interneurons. Kv3.2 subunits are found in all PV-containing neurons in deep cortical layers where they probably form heteromultimeric channels with Kv3.1 subunits. In contrast, in superficial layer PV-positive neurons Kv3.2 immunoreactivity is low, but Kv3.1 is still prominently expressed. Because Kv3.1 and Kv3.2 channels are differentially modulated by protein kinases, these results raise the possibility that the fast-spiking properties of superficial- and deep-layer PV neurons are differentially regulated by neuromodulators. Interestingly, Kv3. 2 but not Kv3.1 proteins are also prominent in a subset of seemingly non-fast-spiking, somatostatin- and calbindin-containing interneurons, suggesting that the Kv3.1-Kv3.2 current type can have functions other than facilitating high-frequency firing.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Axons - physiology</subject><subject>Axons - ultrastructure</subject><subject>Brain - physiology</subject><subject>Cell Line</subject><subject>Cell Membrane - physiology</subject><subject>Cell Membrane - ultrastructure</subject><subject>Dendrites - physiology</subject><subject>Dendrites - ultrastructure</subject><subject>Fast spiking</subject><subject>Fisiologia</subject><subject>GABA</subject><subject>High-frequency firing</subject><subject>Humans</subject><subject>Inhibition</subject><subject>Interneurons - cytology</subject><subject>Interneurons - physiology</subject><subject>Kv3 subunits</subject><subject>Mice</subject><subject>Molecular Sequence Data</subject><subject>Neocortex - cytology</subject><subject>Neocortex - physiology</subject><subject>Neurones</subject><subject>Neurons - classification</subject><subject>Neurons - cytology</subject><subject>Neurons - physiology</subject><subject>Neuropeptides - analysis</subject><subject>Neuropeptides - genetics</subject><subject>Neuropeptides - physiology</subject><subject>Parvalbumins - analysis</subject><subject>Peptide Fragments - chemistry</subject><subject>Peptide Fragments - immunology</subject><subject>Potassium Channels - analysis</subject><subject>Potassium Channels - genetics</subject><subject>Potassium Channels - physiology</subject><subject>Potassium Channels, Voltage-Gated</subject><subject>Rabbits</subject><subject>Rats</subject><subject>Recombinant Proteins - analysis</subject><subject>Recombinant Proteins - metabolism</subject><subject>Shaw Potassium Channels</subject><subject>Somatosensory Cortex - cytology</subject><subject>Somatosensory Cortex - physiology</subject><subject>Somatostatin - analysis</subject><subject>Transfection</subject><subject>Voltage-gated K1 channels</subject><subject>Xarxes neuronals (Neurobiologia)</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>XX2</sourceid><recordid>eNpVkVtv1DAQhSMEokvhL6CIB3hAKb7kZh6QUFhgoWoRS5-tiTPZdZXYi-008O_xXlSVB8sez3eOxzpJ8oqSC1ow_u7W4OSsV_qCiozRjAjOWTwL8ShZRCJe5oQ-ThaEVSQr8yo_S555f0sIqQitniZnlBSc5rxeJPP3t2mzBWNwSJd_dg6919akn7QP2mwm7bfo0_XU7uxuGiDEnk9tn_4AdwdDO43aZCmYLl3bEYL1ISIma6wJoE00SK_QKuuCVjCkKxPQHWY3_nnypIfB44vTfp7cfF7-ar5ml9dfVs3Hy0yVVISsVZhT6Fseq7aquOqIKPK65VDVZS-gLeoaaKcY1koUqiBl3aOCLkeBkQZ-nnw4-u6mdsROoQkOBrlzegT3V1rQ8v-O0Vu5sXeyrGommIgG9Gig_KSkQ4VOQTgI74v9YqRiklFOWRk1r0-POvt7Qh_kqL3CYQCDdvKyFJEWRR3B9yfzmKd32N8PRoncZy2_XS1vfl6vm5WkItrLQ9Zyn3UUv3z4tQfSY7gReHMEtnqznbVD6UcYhohTOc_z0XDvx_8Bk466Tw</recordid><startdate>19991101</startdate><enddate>19991101</enddate><creator>Chow, A</creator><creator>Erisir, A</creator><creator>Farb, C</creator><creator>Nadal, M. S</creator><creator>Ozaita, A</creator><creator>Lau, D</creator><creator>Welker, E</creator><creator>Rudy, B</creator><general>Soc Neuroscience</general><general>Society for Neuroscience</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>XX2</scope><scope>5PM</scope></search><sort><creationdate>19991101</creationdate><title>K+ Channel Expression Distinguishes Subpopulations of Parvalbumin- and Somatostatin-Containing Neocortical Interneurons</title><author>Chow, A ; Erisir, A ; Farb, C ; Nadal, M. S ; Ozaita, A ; Lau, D ; Welker, E ; Rudy, B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c619t-bce41afb3619b773cd09548b3a786f9ab588a1dc2e8c95c5068fecad4e9e73ca3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Antibodies</topic><topic>Axons - physiology</topic><topic>Axons - ultrastructure</topic><topic>Brain - physiology</topic><topic>Cell Line</topic><topic>Cell Membrane - physiology</topic><topic>Cell Membrane - ultrastructure</topic><topic>Dendrites - physiology</topic><topic>Dendrites - ultrastructure</topic><topic>Fast spiking</topic><topic>Fisiologia</topic><topic>GABA</topic><topic>High-frequency firing</topic><topic>Humans</topic><topic>Inhibition</topic><topic>Interneurons - cytology</topic><topic>Interneurons - physiology</topic><topic>Kv3 subunits</topic><topic>Mice</topic><topic>Molecular Sequence Data</topic><topic>Neocortex - cytology</topic><topic>Neocortex - physiology</topic><topic>Neurones</topic><topic>Neurons - classification</topic><topic>Neurons - cytology</topic><topic>Neurons - physiology</topic><topic>Neuropeptides - analysis</topic><topic>Neuropeptides - genetics</topic><topic>Neuropeptides - physiology</topic><topic>Parvalbumins - analysis</topic><topic>Peptide Fragments - chemistry</topic><topic>Peptide Fragments - immunology</topic><topic>Potassium Channels - analysis</topic><topic>Potassium Channels - genetics</topic><topic>Potassium Channels - physiology</topic><topic>Potassium Channels, Voltage-Gated</topic><topic>Rabbits</topic><topic>Rats</topic><topic>Recombinant Proteins - analysis</topic><topic>Recombinant Proteins - metabolism</topic><topic>Shaw Potassium Channels</topic><topic>Somatosensory Cortex - cytology</topic><topic>Somatosensory Cortex - physiology</topic><topic>Somatostatin - analysis</topic><topic>Transfection</topic><topic>Voltage-gated K1 channels</topic><topic>Xarxes neuronals (Neurobiologia)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chow, A</creatorcontrib><creatorcontrib>Erisir, A</creatorcontrib><creatorcontrib>Farb, C</creatorcontrib><creatorcontrib>Nadal, M. S</creatorcontrib><creatorcontrib>Ozaita, A</creatorcontrib><creatorcontrib>Lau, D</creatorcontrib><creatorcontrib>Welker, E</creatorcontrib><creatorcontrib>Rudy, B</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Recercat</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chow, A</au><au>Erisir, A</au><au>Farb, C</au><au>Nadal, M. S</au><au>Ozaita, A</au><au>Lau, D</au><au>Welker, E</au><au>Rudy, B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>K+ Channel Expression Distinguishes Subpopulations of Parvalbumin- and Somatostatin-Containing Neocortical Interneurons</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>1999-11-01</date><risdate>1999</risdate><volume>19</volume><issue>21</issue><spage>9332</spage><epage>9345</epage><pages>9332-9345</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>Kv3.1 and Kv3.2 K(+) channel proteins form similar voltage-gated K(+) channels with unusual properties, including fast activation at voltages positive to -10 mV and very fast deactivation rates. These properties are thought to facilitate sustained high-frequency firing. Kv3.1 subunits are specifically found in fast-spiking, parvalbumin (PV)-containing cortical interneurons, and recent studies have provided support for a crucial role in the generation of the fast-spiking phenotype. Kv3.2 mRNAs are also found in a small subset of neocortical neurons, although the distribution of these neurons is different. We raised antibodies directed against Kv3.2 proteins and used dual-labeling methods to identify the neocortical neurons expressing Kv3.2 proteins and to determine their subcellular localization. Kv3.2 proteins are prominently expressed in patches in somatic and proximal dendritic membrane as well as in axons and presynaptic terminals of GABAergic interneurons. Kv3.2 subunits are found in all PV-containing neurons in deep cortical layers where they probably form heteromultimeric channels with Kv3.1 subunits. In contrast, in superficial layer PV-positive neurons Kv3.2 immunoreactivity is low, but Kv3.1 is still prominently expressed. Because Kv3.1 and Kv3.2 channels are differentially modulated by protein kinases, these results raise the possibility that the fast-spiking properties of superficial- and deep-layer PV neurons are differentially regulated by neuromodulators. Interestingly, Kv3. 2 but not Kv3.1 proteins are also prominent in a subset of seemingly non-fast-spiking, somatostatin- and calbindin-containing interneurons, suggesting that the Kv3.1-Kv3.2 current type can have functions other than facilitating high-frequency firing.</abstract><cop>United States</cop><pub>Soc Neuroscience</pub><pmid>10531438</pmid><doi>10.1523/jneurosci.19-21-09332.1999</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Animals Antibodies Axons - physiology Axons - ultrastructure Brain - physiology Cell Line Cell Membrane - physiology Cell Membrane - ultrastructure Dendrites - physiology Dendrites - ultrastructure Fast spiking Fisiologia GABA High-frequency firing Humans Inhibition Interneurons - cytology Interneurons - physiology Kv3 subunits Mice Molecular Sequence Data Neocortex - cytology Neocortex - physiology Neurones Neurons - classification Neurons - cytology Neurons - physiology Neuropeptides - analysis Neuropeptides - genetics Neuropeptides - physiology Parvalbumins - analysis Peptide Fragments - chemistry Peptide Fragments - immunology Potassium Channels - analysis Potassium Channels - genetics Potassium Channels - physiology Potassium Channels, Voltage-Gated Rabbits Rats Recombinant Proteins - analysis Recombinant Proteins - metabolism Shaw Potassium Channels Somatosensory Cortex - cytology Somatosensory Cortex - physiology Somatostatin - analysis Transfection Voltage-gated K1 channels Xarxes neuronals (Neurobiologia) |
title | K+ Channel Expression Distinguishes Subpopulations of Parvalbumin- and Somatostatin-Containing Neocortical Interneurons |
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