Developmental changes in the expression of potassium currents of embryonic, neonatal and mature mouse inner hair cells

Developmental changes in electrophysiological membrane properties of mouse cochlear inner hair cells (IHCs) were studied from just after terminal differentiation up to functional maturity. As early as embryonic day 14.5 (E14.5) newly differentiated IHCs express a very small outward K + current that...

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Veröffentlicht in:The Journal of physiology 2003-04, Vol.548 (2), p.383-400
Hauptverfasser: Marcotti, Walter, Johnson, Stuart L, Holley, Matthew C, Kros, Corné J
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Kros, Corné J
description Developmental changes in electrophysiological membrane properties of mouse cochlear inner hair cells (IHCs) were studied from just after terminal differentiation up to functional maturity. As early as embryonic day 14.5 (E14.5) newly differentiated IHCs express a very small outward K + current that is largely insensitive to 4-aminopyridine (4-AP). One day later the inward rectifier, I K1 , is first observed. These immature cells initially exhibit only slow graded voltage responses under current clamp. From E17.5 spontaneous action potentials occur. During the first week of postnatal development, the outward K + current steadily increases in size and a progressively larger fraction of the current is sensitive to 4-AP. During the second postnatal week, the activation of the 4-AP-sensitive current, by now contributing about half of the outward K + current, shifts in the hyperpolarizing direction. Together with an increase in size of I K1 , this hyperpolarizes the cell, thus inhibiting the spontaneous spike activity, although spikes could still be evoked upon depolarizing current injection. Starting at about the onset of hearing (postnatal day 12, P12) immature IHCs make the final steps towards fully functional sensory receptors with fast graded voltage responses. This is achieved mainly by the expression of the large-conductance Ca 2+ -activated K + current I K,f , but also of a current indistinguishable from the negatively activating I K,n previously described in mature outer hair cells (OHCs). The 4-AP-sensitive current continues to increase after the onset of hearing to form the major part of the mature delayed rectifier, I K,s . By P20 IHCs appear mature in terms of their complement of K + conductances.
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As early as embryonic day 14.5 (E14.5) newly differentiated IHCs express a very small outward K + current that is largely insensitive to 4-aminopyridine (4-AP). One day later the inward rectifier, I K1 , is first observed. These immature cells initially exhibit only slow graded voltage responses under current clamp. From E17.5 spontaneous action potentials occur. During the first week of postnatal development, the outward K + current steadily increases in size and a progressively larger fraction of the current is sensitive to 4-AP. During the second postnatal week, the activation of the 4-AP-sensitive current, by now contributing about half of the outward K + current, shifts in the hyperpolarizing direction. Together with an increase in size of I K1 , this hyperpolarizes the cell, thus inhibiting the spontaneous spike activity, although spikes could still be evoked upon depolarizing current injection. 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As early as embryonic day 14.5 (E14.5) newly differentiated IHCs express a very small outward K + current that is largely insensitive to 4-aminopyridine (4-AP). One day later the inward rectifier, I K1 , is first observed. These immature cells initially exhibit only slow graded voltage responses under current clamp. From E17.5 spontaneous action potentials occur. During the first week of postnatal development, the outward K + current steadily increases in size and a progressively larger fraction of the current is sensitive to 4-AP. During the second postnatal week, the activation of the 4-AP-sensitive current, by now contributing about half of the outward K + current, shifts in the hyperpolarizing direction. Together with an increase in size of I K1 , this hyperpolarizes the cell, thus inhibiting the spontaneous spike activity, although spikes could still be evoked upon depolarizing current injection. Starting at about the onset of hearing (postnatal day 12, P12) immature IHCs make the final steps towards fully functional sensory receptors with fast graded voltage responses. This is achieved mainly by the expression of the large-conductance Ca 2+ -activated K + current I K,f , but also of a current indistinguishable from the negatively activating I K,n previously described in mature outer hair cells (OHCs). The 4-AP-sensitive current continues to increase after the onset of hearing to form the major part of the mature delayed rectifier, I K,s . By P20 IHCs appear mature in terms of their complement of K + conductances.</description><subject>4-Aminopyridine - pharmacology</subject><subject>Algorithms</subject><subject>Animals</subject><subject>Animals, Newborn - metabolism</subject><subject>Calcium Channels - drug effects</subject><subject>Calcium Channels - metabolism</subject><subject>Cochlea - cytology</subject><subject>Cochlea - embryology</subject><subject>Cochlea - growth &amp; development</subject><subject>Electrophysiology</subject><subject>Female</subject><subject>Hair Cells, Auditory, Inner - embryology</subject><subject>Hair Cells, Auditory, Inner - growth &amp; development</subject><subject>Hair Cells, Auditory, Inner - metabolism</subject><subject>Indoles - pharmacology</subject><subject>Large-Conductance Calcium-Activated Potassium Channels</subject><subject>Membrane Potentials - physiology</subject><subject>Mice</subject><subject>Original</subject><subject>Patch-Clamp Techniques</subject><subject>Potassium Channel Blockers - pharmacology</subject><subject>Potassium Channels - biosynthesis</subject><subject>Potassium Channels, Calcium-Activated - drug effects</subject><subject>Potassium Channels, Calcium-Activated - metabolism</subject><subject>Potassium Channels, Inwardly Rectifying - drug effects</subject><subject>Potassium Channels, Inwardly Rectifying - metabolism</subject><subject>Pregnancy</subject><subject>Pyridines - pharmacology</subject><issn>0022-3751</issn><issn>1469-7793</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkUtv1DAUhS1ERYfCP0DIK9iQwa-MnQ1SVV6VKnUDa8tj30xcJXawk4H593WU4bWy7HvOd-_1QegVJVtKKX__MHan7GO_ZYSwLeFCEfoEbajYNZWUDX-KNqXAKi5reome5_xACOWkaZ6hS8pqpVQjN-j4EY7Qx3GAMJke286EA2TsA546wPBrTJBLl4Bji8c4mXKZB2znlIohL68w7NMpBm_f4QAxmAVjgsODmeYEeIhzhsILkHBnfMIW-j6_QBet6TO8PJ9X6PvnT99uvlZ3919ub67vKiu4mCqmuGpr65ho1E4yqiw0-8Y5arlznElVM07afcuIda1S1O2MbXYCwDFLjDP8Cn1YueO8H8DZMnQyvR6TH0w66Wi8_r8SfKcP8agZF0wJVgBvzoAUf8yQJz34vKxgyrJz1pJTKctnFqFYhTbFnBO0f5pQopfA9O_A9BKYXgMrttf_DvjXdE6oCN6ugs4fup8-gV4xOVoP00nXQmmmueL8EbSlpqA</recordid><startdate>20030415</startdate><enddate>20030415</enddate><creator>Marcotti, Walter</creator><creator>Johnson, Stuart L</creator><creator>Holley, Matthew C</creator><creator>Kros, Corné J</creator><general>The Physiological Society</general><general>Blackwell Science Inc</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>5PM</scope></search><sort><creationdate>20030415</creationdate><title>Developmental changes in the expression of potassium currents of embryonic, neonatal and mature mouse inner hair cells</title><author>Marcotti, Walter ; Johnson, Stuart L ; Holley, Matthew C ; Kros, Corné J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-2838f5cd249867218ce9b9dd1c3dd32785230fbf20cdf881d6ac964eed2c0ada3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>4-Aminopyridine - pharmacology</topic><topic>Algorithms</topic><topic>Animals</topic><topic>Animals, Newborn - metabolism</topic><topic>Calcium Channels - drug effects</topic><topic>Calcium Channels - metabolism</topic><topic>Cochlea - cytology</topic><topic>Cochlea - embryology</topic><topic>Cochlea - growth &amp; development</topic><topic>Electrophysiology</topic><topic>Female</topic><topic>Hair Cells, Auditory, Inner - embryology</topic><topic>Hair Cells, Auditory, Inner - growth &amp; development</topic><topic>Hair Cells, Auditory, Inner - metabolism</topic><topic>Indoles - pharmacology</topic><topic>Large-Conductance Calcium-Activated Potassium Channels</topic><topic>Membrane Potentials - physiology</topic><topic>Mice</topic><topic>Original</topic><topic>Patch-Clamp Techniques</topic><topic>Potassium Channel Blockers - pharmacology</topic><topic>Potassium Channels - biosynthesis</topic><topic>Potassium Channels, Calcium-Activated - drug effects</topic><topic>Potassium Channels, Calcium-Activated - metabolism</topic><topic>Potassium Channels, Inwardly Rectifying - drug effects</topic><topic>Potassium Channels, Inwardly Rectifying - metabolism</topic><topic>Pregnancy</topic><topic>Pyridines - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marcotti, Walter</creatorcontrib><creatorcontrib>Johnson, Stuart L</creatorcontrib><creatorcontrib>Holley, Matthew C</creatorcontrib><creatorcontrib>Kros, Corné J</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>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marcotti, Walter</au><au>Johnson, Stuart L</au><au>Holley, Matthew C</au><au>Kros, Corné J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Developmental changes in the expression of potassium currents of embryonic, neonatal and mature mouse inner hair cells</atitle><jtitle>The Journal of physiology</jtitle><addtitle>J Physiol</addtitle><date>2003-04-15</date><risdate>2003</risdate><volume>548</volume><issue>2</issue><spage>383</spage><epage>400</epage><pages>383-400</pages><issn>0022-3751</issn><eissn>1469-7793</eissn><abstract>Developmental changes in electrophysiological membrane properties of mouse cochlear inner hair cells (IHCs) were studied from just after terminal differentiation up to functional maturity. As early as embryonic day 14.5 (E14.5) newly differentiated IHCs express a very small outward K + current that is largely insensitive to 4-aminopyridine (4-AP). One day later the inward rectifier, I K1 , is first observed. These immature cells initially exhibit only slow graded voltage responses under current clamp. From E17.5 spontaneous action potentials occur. During the first week of postnatal development, the outward K + current steadily increases in size and a progressively larger fraction of the current is sensitive to 4-AP. During the second postnatal week, the activation of the 4-AP-sensitive current, by now contributing about half of the outward K + current, shifts in the hyperpolarizing direction. Together with an increase in size of I K1 , this hyperpolarizes the cell, thus inhibiting the spontaneous spike activity, although spikes could still be evoked upon depolarizing current injection. Starting at about the onset of hearing (postnatal day 12, P12) immature IHCs make the final steps towards fully functional sensory receptors with fast graded voltage responses. This is achieved mainly by the expression of the large-conductance Ca 2+ -activated K + current I K,f , but also of a current indistinguishable from the negatively activating I K,n previously described in mature outer hair cells (OHCs). The 4-AP-sensitive current continues to increase after the onset of hearing to form the major part of the mature delayed rectifier, I K,s . By P20 IHCs appear mature in terms of their complement of K + conductances.</abstract><cop>England</cop><pub>The Physiological Society</pub><pmid>12588897</pmid><doi>10.1113/jphysiol.2002.034801</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record>
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subjects 4-Aminopyridine - pharmacology
Algorithms
Animals
Animals, Newborn - metabolism
Calcium Channels - drug effects
Calcium Channels - metabolism
Cochlea - cytology
Cochlea - embryology
Cochlea - growth & development
Electrophysiology
Female
Hair Cells, Auditory, Inner - embryology
Hair Cells, Auditory, Inner - growth & development
Hair Cells, Auditory, Inner - metabolism
Indoles - pharmacology
Large-Conductance Calcium-Activated Potassium Channels
Membrane Potentials - physiology
Mice
Original
Patch-Clamp Techniques
Potassium Channel Blockers - pharmacology
Potassium Channels - biosynthesis
Potassium Channels, Calcium-Activated - drug effects
Potassium Channels, Calcium-Activated - metabolism
Potassium Channels, Inwardly Rectifying - drug effects
Potassium Channels, Inwardly Rectifying - metabolism
Pregnancy
Pyridines - pharmacology
title Developmental changes in the expression of potassium currents of embryonic, neonatal and mature mouse inner hair cells
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