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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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. |
doi_str_mv | 10.1016/j.brainres.2007.12.048 |
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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><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/j.brainres.2007.12.048</identifier><identifier>PMID: 18241843</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>London: Elsevier B.V</publisher><subject>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</subject><ispartof>Brain research, 2008-03, Vol.1197, p.76-84</ispartof><rights>Elsevier B.V.</rights><rights>2007 Elsevier B.V.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c482t-78c842063790df5801b93f0a2c1cc76031270fc0929d04f9c03fa8256c07cb23</citedby><cites>FETCH-LOGICAL-c482t-78c842063790df5801b93f0a2c1cc76031270fc0929d04f9c03fa8256c07cb23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.brainres.2007.12.048$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20141328$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18241843$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Horowitz, Seth S</creatorcontrib><creatorcontrib>Stamper, Sarah A</creatorcontrib><creatorcontrib>Simmons, James A</creatorcontrib><title>Neuronal connexin expression in the cochlear nucleus of big brown bats</title><title>Brain research</title><addtitle>Brain Res</addtitle><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.</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 ). 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.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>18241843</pmid><doi>10.1016/j.brainres.2007.12.048</doi><tpages>9</tpages></addata></record> |
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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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