Neuronal connexin expression in the cochlear nucleus of big brown bats

Abstract We present immunohistochemical data describing the presence and distribution of connexins, structural component of gap junctions, in the cochlear nuclei of adult big brown bats ( Eptesicus fuscus ). Echolocating big brown bats show microsecond scale echo-delay sensitivity that requires accu...

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Veröffentlicht in:Brain research 2008-03, Vol.1197, p.76-84
Hauptverfasser: Horowitz, Seth S, Stamper, Sarah A, Simmons, James A
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Simmons, James A
description Abstract We present immunohistochemical data describing the presence and distribution of connexins, structural component of gap junctions, in the cochlear nuclei of adult big brown bats ( Eptesicus fuscus ). Echolocating big brown bats show microsecond scale echo-delay sensitivity that requires accurate synchronization of neuronal responses to the timing of echoes. Midbrain and auditory cortical neuronal response timing is similar to that observed in other non-echolocating mammals, suggesting that lower auditory processing nuclei may have specialized mechanisms for obtaining the required temporal hyperacuity. Our data shows that connexin 36, a gap junction protein specific to neurons, is most densely expressed in the bat's cochlear nuclear complex, the medullary region that receives and processes first-order afferents from the auditory nerve. Cx36 expression is absent in the cochlear nucleus of normal mice, which have high-frequency hearing sensitivity similar to big brown bats. Glial connexins, Cx26 and Cx43, expressed in astrocytes and several inner ear structures, are also found in the bat cochlear nucleus complex, associated with major fiber tracts in and around the cochlear nuclei. The extensive presence of neuronally-associated Cx36 in brainstem auditory structures of adult bats suggests a possible role for gap junctions in mediating echo-delay hyperacuity.
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Echolocating big brown bats show microsecond scale echo-delay sensitivity that requires accurate synchronization of neuronal responses to the timing of echoes. Midbrain and auditory cortical neuronal response timing is similar to that observed in other non-echolocating mammals, suggesting that lower auditory processing nuclei may have specialized mechanisms for obtaining the required temporal hyperacuity. Our data shows that connexin 36, a gap junction protein specific to neurons, is most densely expressed in the bat's cochlear nuclear complex, the medullary region that receives and processes first-order afferents from the auditory nerve. Cx36 expression is absent in the cochlear nucleus of normal mice, which have high-frequency hearing sensitivity similar to big brown bats. Glial connexins, Cx26 and Cx43, expressed in astrocytes and several inner ear structures, are also found in the bat cochlear nucleus complex, associated with major fiber tracts in and around the cochlear nuclei. 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Echolocating big brown bats show microsecond scale echo-delay sensitivity that requires accurate synchronization of neuronal responses to the timing of echoes. Midbrain and auditory cortical neuronal response timing is similar to that observed in other non-echolocating mammals, suggesting that lower auditory processing nuclei may have specialized mechanisms for obtaining the required temporal hyperacuity. Our data shows that connexin 36, a gap junction protein specific to neurons, is most densely expressed in the bat's cochlear nuclear complex, the medullary region that receives and processes first-order afferents from the auditory nerve. Cx36 expression is absent in the cochlear nucleus of normal mice, which have high-frequency hearing sensitivity similar to big brown bats. Glial connexins, Cx26 and Cx43, expressed in astrocytes and several inner ear structures, are also found in the bat cochlear nucleus complex, associated with major fiber tracts in and around the cochlear nuclei. The extensive presence of neuronally-associated Cx36 in brainstem auditory structures of adult bats suggests a possible role for gap junctions in mediating echo-delay hyperacuity.</description><subject>Animals</subject><subject>Bat</subject><subject>Biological and medical sciences</subject><subject>Chiroptera - physiology</subject><subject>Cochlear nucleus</subject><subject>Cochlear Nucleus - metabolism</subject><subject>Connexin</subject><subject>Connexins - biosynthesis</subject><subject>Ear and associated structures. Auditory pathways and centers. Hearing. Vocal organ. Phonation. Sound production. Echolocation</subject><subject>Echolocation</subject><subject>Eptesicus fuscus</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gap junction</subject><subject>Gap Junction delta-2 Protein</subject><subject>Immunohistochemistry</subject><subject>Microscopy, Confocal</subject><subject>Neurology</subject><subject>Neurons - metabolism</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFksFu1DAQhi0EokvhFapc4JYwtrOxfUGgigJSBQd6t5zJhHrJ2oudQPv2ONoFJC49WSN_84_1eRi74NBw4N3rXdMn50Oi3AgA1XDRQKsfsQ3XStSdaOEx2wBAV2tj5Bl7lvOulFIaeMrOuBYt163csKvPtKQY3FRhDIHufKjo7lBis4-hKtV8S-UKbydyqQoLTrTkKo5V779VfYq_QtW7OT9nT0Y3ZXpxOs_ZzdX7m8uP9fWXD58u313X2Gox10qjbgV0UhkYxq0G3hs5ghPIEVUHkgsFI4IRZoB2NAhydFpsOwSFvZDn7NUx9pDij4XybPc-I02TCxSXbBVI0Bz0g6CArRKqlQXsjiCmmHOi0R6S37t0bznY1bTd2T-m7WracmGL6dJ4cZqw9Hsa_rWd1Bbg5QlwGd00JhfQ57-cAN5yKdagt0eOirefnpLN6CkgDT4RznaI_uG3vPkvAicffJn6ne4p7-KSyg9ny20uDfbruhfrWsDqCwzI3_XTsyc</recordid><startdate>20080304</startdate><enddate>20080304</enddate><creator>Horowitz, Seth S</creator><creator>Stamper, Sarah A</creator><creator>Simmons, James A</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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>7TK</scope><scope>7X8</scope></search><sort><creationdate>20080304</creationdate><title>Neuronal connexin expression in the cochlear nucleus of big brown bats</title><author>Horowitz, Seth S ; Stamper, Sarah A ; Simmons, James A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c482t-78c842063790df5801b93f0a2c1cc76031270fc0929d04f9c03fa8256c07cb23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Bat</topic><topic>Biological and medical sciences</topic><topic>Chiroptera - physiology</topic><topic>Cochlear nucleus</topic><topic>Cochlear Nucleus - metabolism</topic><topic>Connexin</topic><topic>Connexins - biosynthesis</topic><topic>Ear and associated structures. Auditory pathways and centers. Hearing. Vocal organ. Phonation. Sound production. Echolocation</topic><topic>Echolocation</topic><topic>Eptesicus fuscus</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gap junction</topic><topic>Gap Junction delta-2 Protein</topic><topic>Immunohistochemistry</topic><topic>Microscopy, Confocal</topic><topic>Neurology</topic><topic>Neurons - metabolism</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Horowitz, Seth S</creatorcontrib><creatorcontrib>Stamper, Sarah A</creatorcontrib><creatorcontrib>Simmons, James A</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Horowitz, Seth S</au><au>Stamper, Sarah A</au><au>Simmons, James A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neuronal connexin expression in the cochlear nucleus of big brown bats</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>2008-03-04</date><risdate>2008</risdate><volume>1197</volume><spage>76</spage><epage>84</epage><pages>76-84</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>Abstract We present immunohistochemical data describing the presence and distribution of connexins, structural component of gap junctions, in the cochlear nuclei of adult big brown bats ( Eptesicus fuscus ). 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subjects Animals
Bat
Biological and medical sciences
Chiroptera - physiology
Cochlear nucleus
Cochlear Nucleus - metabolism
Connexin
Connexins - biosynthesis
Ear and associated structures. Auditory pathways and centers. Hearing. Vocal organ. Phonation. Sound production. Echolocation
Echolocation
Eptesicus fuscus
Fundamental and applied biological sciences. Psychology
Gap junction
Gap Junction delta-2 Protein
Immunohistochemistry
Microscopy, Confocal
Neurology
Neurons - metabolism
Vertebrates: nervous system and sense organs
title Neuronal connexin expression in the cochlear nucleus of big brown bats
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