Characteristics of A-type voltage-gated K+ currents expressed on sour-sensing type III taste receptor cells in mice
Sour taste is detected by type III taste receptor cells that generate membrane depolarization with action potentials in response to HCl applied to the apical membranes. The shape of action potentials in type III cells exhibits larger afterhyperpolarization due to activation of transient A-type volta...
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description | Sour taste is detected by type III taste receptor cells that generate membrane depolarization with action potentials in response to HCl applied to the apical membranes. The shape of action potentials in type III cells exhibits larger afterhyperpolarization due to activation of transient A-type voltage-gated K
+
currents. Although action potentials play an important role in neurotransmitter release, the electrophysiological features of A-type K
+
currents in taste buds remain unclear. Here, we examined the electrophysiological properties of A-type K
+
currents in mouse fungiform taste bud cells using in-situ whole-cell patch clamping. Type III cells were identified with SNAP-25 immunoreactivity and/or electrophysiological features of voltage-gated currents. Type III cells expressed A-type K
+
currents which were completely inhibited by 10 mM TEA, whereas IP
3
R3-immunoreactive type II cells did not. The half-maximal activation and steady-state inactivation of A-type K
+
currents were 17.9 ± 4.5 (n = 17) and − 11.0 ± 5.7 (n = 17) mV, respectively, which are similar to the features of Kv3.3 and Kv3.4 channels (transient and high voltage-activated K
+
channels). The recovery from inactivation was well fitted with a double exponential equation; the fast and slow time constants were 6.4 ± 0.6 ms and 0.76 ± 0.26 s (n = 6), respectively. RT-PCR experiments suggest that Kv3.3 and Kv3.4 mRNAs were detected at the taste bud level, but not at single-cell levels. As the phosphorylation of Kv3.3 and Kv3.4 channels generally leads to the modulation of cell excitability, neuromodulator-mediated A-type K
+
channel phosphorylation likely affects the signal transduction of taste. |
doi_str_mv | 10.1007/s00441-024-03887-6 |
format | Article |
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+
currents. Although action potentials play an important role in neurotransmitter release, the electrophysiological features of A-type K
+
currents in taste buds remain unclear. Here, we examined the electrophysiological properties of A-type K
+
currents in mouse fungiform taste bud cells using in-situ whole-cell patch clamping. Type III cells were identified with SNAP-25 immunoreactivity and/or electrophysiological features of voltage-gated currents. Type III cells expressed A-type K
+
currents which were completely inhibited by 10 mM TEA, whereas IP
3
R3-immunoreactive type II cells did not. The half-maximal activation and steady-state inactivation of A-type K
+
currents were 17.9 ± 4.5 (n = 17) and − 11.0 ± 5.7 (n = 17) mV, respectively, which are similar to the features of Kv3.3 and Kv3.4 channels (transient and high voltage-activated K
+
channels). The recovery from inactivation was well fitted with a double exponential equation; the fast and slow time constants were 6.4 ± 0.6 ms and 0.76 ± 0.26 s (n = 6), respectively. RT-PCR experiments suggest that Kv3.3 and Kv3.4 mRNAs were detected at the taste bud level, but not at single-cell levels. As the phosphorylation of Kv3.3 and Kv3.4 channels generally leads to the modulation of cell excitability, neuromodulator-mediated A-type K
+
channel phosphorylation likely affects the signal transduction of taste.</description><identifier>ISSN: 0302-766X</identifier><identifier>ISSN: 1432-0878</identifier><identifier>EISSN: 1432-0878</identifier><identifier>DOI: 10.1007/s00441-024-03887-6</identifier><identifier>PMID: 38492001</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Afterhyperpolarization ; Biomedical and Life Sciences ; Biomedicine ; Channel gating ; Depolarization ; Excitability ; Human Genetics ; Immunoreactivity ; Membrane potential ; Molecular Medicine ; Neuromodulation ; Neurotransmitter release ; Phosphorylation ; Potassium channels (voltage-gated) ; Proteomics ; Regular ; Regular Article ; Signal transduction ; SNAP-25 protein ; Sour taste ; Taste buds ; Taste receptor neurons ; Taste receptors</subject><ispartof>Cell and tissue research, 2024-06, Vol.396 (3), p.353-369</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c470t-d0e4266badcca4932e22f1906609aa36088d255bc383eac5680b0b0046323ba43</cites><orcidid>0000-0002-3413-5478</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00441-024-03887-6$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00441-024-03887-6$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38492001$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moribayashi, Takeru</creatorcontrib><creatorcontrib>Nakao, Yoshiki</creatorcontrib><creatorcontrib>Ohtubo, Yoshitaka</creatorcontrib><title>Characteristics of A-type voltage-gated K+ currents expressed on sour-sensing type III taste receptor cells in mice</title><title>Cell and tissue research</title><addtitle>Cell Tissue Res</addtitle><addtitle>Cell Tissue Res</addtitle><description>Sour taste is detected by type III taste receptor cells that generate membrane depolarization with action potentials in response to HCl applied to the apical membranes. The shape of action potentials in type III cells exhibits larger afterhyperpolarization due to activation of transient A-type voltage-gated K
+
currents. Although action potentials play an important role in neurotransmitter release, the electrophysiological features of A-type K
+
currents in taste buds remain unclear. Here, we examined the electrophysiological properties of A-type K
+
currents in mouse fungiform taste bud cells using in-situ whole-cell patch clamping. Type III cells were identified with SNAP-25 immunoreactivity and/or electrophysiological features of voltage-gated currents. Type III cells expressed A-type K
+
currents which were completely inhibited by 10 mM TEA, whereas IP
3
R3-immunoreactive type II cells did not. The half-maximal activation and steady-state inactivation of A-type K
+
currents were 17.9 ± 4.5 (n = 17) and − 11.0 ± 5.7 (n = 17) mV, respectively, which are similar to the features of Kv3.3 and Kv3.4 channels (transient and high voltage-activated K
+
channels). The recovery from inactivation was well fitted with a double exponential equation; the fast and slow time constants were 6.4 ± 0.6 ms and 0.76 ± 0.26 s (n = 6), respectively. RT-PCR experiments suggest that Kv3.3 and Kv3.4 mRNAs were detected at the taste bud level, but not at single-cell levels. As the phosphorylation of Kv3.3 and Kv3.4 channels generally leads to the modulation of cell excitability, neuromodulator-mediated A-type K
+
channel phosphorylation likely affects the signal transduction of taste.</description><subject>Afterhyperpolarization</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Channel gating</subject><subject>Depolarization</subject><subject>Excitability</subject><subject>Human Genetics</subject><subject>Immunoreactivity</subject><subject>Membrane potential</subject><subject>Molecular Medicine</subject><subject>Neuromodulation</subject><subject>Neurotransmitter release</subject><subject>Phosphorylation</subject><subject>Potassium channels (voltage-gated)</subject><subject>Proteomics</subject><subject>Regular</subject><subject>Regular Article</subject><subject>Signal transduction</subject><subject>SNAP-25 protein</subject><subject>Sour taste</subject><subject>Taste buds</subject><subject>Taste receptor neurons</subject><subject>Taste receptors</subject><issn>0302-766X</issn><issn>1432-0878</issn><issn>1432-0878</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><recordid>eNp9kU1v1DAQhi0EokvhD3BAlrggIcPEdhznhKoVHysqcQGJm-U4s2mqbLx4nKr993i7pXwckA-WPc-88_Ey9ryCNxVA85YAtK4ESC1AWdsI84CtKq2kANvYh2wFCqRojPl-wp4QXQJU2pj2MTtRVreyPFeM1hc--ZAxjZTHQDxu-ZnIN3vkV3HKfkAx-Iw9__yahyUlnDNxvN4nJCq_ceYUlyQIZxrngd8mbjYbnj1l5AkD7nNMPOA0ER9nvhsDPmWPtn4ifHZ3n7JvH95_XX8S518-btZn5yLoBrLoAbU0pvN9CF63SqKU26oFY6D1Xhmwtpd13QVlFfpQGwtdOaCNkqrzWp2yd0fd_dLtsA-l9-Qnt0_jzqcbF_3o_o7M44Ub4pWrqqosVpmi8OpOIcUfC1J2u5EOs_gZ40JOtrWVrZSmLujLf9DLspi5zOcUmAJqsKpQ8kiFFIkSbu-7qcAdTHVHU10x1d2a6g5dvPhzjvuUXy4WQB0BKqF5wPS79n9kfwJ3Ya3C</recordid><startdate>20240601</startdate><enddate>20240601</enddate><creator>Moribayashi, Takeru</creator><creator>Nakao, Yoshiki</creator><creator>Ohtubo, Yoshitaka</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7SS</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3413-5478</orcidid></search><sort><creationdate>20240601</creationdate><title>Characteristics of A-type voltage-gated K+ currents expressed on sour-sensing type III taste receptor cells in mice</title><author>Moribayashi, Takeru ; Nakao, Yoshiki ; Ohtubo, Yoshitaka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-d0e4266badcca4932e22f1906609aa36088d255bc383eac5680b0b0046323ba43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Afterhyperpolarization</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Channel gating</topic><topic>Depolarization</topic><topic>Excitability</topic><topic>Human Genetics</topic><topic>Immunoreactivity</topic><topic>Membrane potential</topic><topic>Molecular Medicine</topic><topic>Neuromodulation</topic><topic>Neurotransmitter release</topic><topic>Phosphorylation</topic><topic>Potassium channels (voltage-gated)</topic><topic>Proteomics</topic><topic>Regular</topic><topic>Regular Article</topic><topic>Signal transduction</topic><topic>SNAP-25 protein</topic><topic>Sour taste</topic><topic>Taste buds</topic><topic>Taste receptor neurons</topic><topic>Taste receptors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moribayashi, Takeru</creatorcontrib><creatorcontrib>Nakao, Yoshiki</creatorcontrib><creatorcontrib>Ohtubo, Yoshitaka</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cell and tissue research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moribayashi, Takeru</au><au>Nakao, Yoshiki</au><au>Ohtubo, Yoshitaka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characteristics of A-type voltage-gated K+ currents expressed on sour-sensing type III taste receptor cells in mice</atitle><jtitle>Cell and tissue research</jtitle><stitle>Cell Tissue Res</stitle><addtitle>Cell Tissue Res</addtitle><date>2024-06-01</date><risdate>2024</risdate><volume>396</volume><issue>3</issue><spage>353</spage><epage>369</epage><pages>353-369</pages><issn>0302-766X</issn><issn>1432-0878</issn><eissn>1432-0878</eissn><abstract>Sour taste is detected by type III taste receptor cells that generate membrane depolarization with action potentials in response to HCl applied to the apical membranes. The shape of action potentials in type III cells exhibits larger afterhyperpolarization due to activation of transient A-type voltage-gated K
+
currents. Although action potentials play an important role in neurotransmitter release, the electrophysiological features of A-type K
+
currents in taste buds remain unclear. Here, we examined the electrophysiological properties of A-type K
+
currents in mouse fungiform taste bud cells using in-situ whole-cell patch clamping. Type III cells were identified with SNAP-25 immunoreactivity and/or electrophysiological features of voltage-gated currents. Type III cells expressed A-type K
+
currents which were completely inhibited by 10 mM TEA, whereas IP
3
R3-immunoreactive type II cells did not. The half-maximal activation and steady-state inactivation of A-type K
+
currents were 17.9 ± 4.5 (n = 17) and − 11.0 ± 5.7 (n = 17) mV, respectively, which are similar to the features of Kv3.3 and Kv3.4 channels (transient and high voltage-activated K
+
channels). The recovery from inactivation was well fitted with a double exponential equation; the fast and slow time constants were 6.4 ± 0.6 ms and 0.76 ± 0.26 s (n = 6), respectively. RT-PCR experiments suggest that Kv3.3 and Kv3.4 mRNAs were detected at the taste bud level, but not at single-cell levels. As the phosphorylation of Kv3.3 and Kv3.4 channels generally leads to the modulation of cell excitability, neuromodulator-mediated A-type K
+
channel phosphorylation likely affects the signal transduction of taste.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>38492001</pmid><doi>10.1007/s00441-024-03887-6</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0002-3413-5478</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Afterhyperpolarization Biomedical and Life Sciences Biomedicine Channel gating Depolarization Excitability Human Genetics Immunoreactivity Membrane potential Molecular Medicine Neuromodulation Neurotransmitter release Phosphorylation Potassium channels (voltage-gated) Proteomics Regular Regular Article Signal transduction SNAP-25 protein Sour taste Taste buds Taste receptor neurons Taste receptors |
title | Characteristics of A-type voltage-gated K+ currents expressed on sour-sensing type III taste receptor cells in mice |
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