Loading…

Role of BDNF and neurotrophic receptors in human inner ear development

The expression patterns of the neurotrophin, brain-derived neurotrophic factor, BDNF, and the neurotrophic receptors—p75NTR and Trk receptors—in the developing human fetal inner ear between the gestational weeks (GW) 9 to 12 are examined via in situ hybridization and immunohistochemistry. BDNF mRNA...

Full description

Saved in:
Bibliographic Details
Published in:Cell and tissue research 2017-12, Vol.370 (3), p.347-363
Main Authors: Johnson Chacko, L., Blumer, M. J. F., Pechriggl, E., Rask-Andersen, H., Dietl, W., Haim, A., Fritsch, H., Glueckert, R., Dudas, J., Schrott-Fischer, A.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c550t-56155f43b5a923741b3a07ad05a66ce11595e24bae3711647d51cecfd22072833
cites cdi_FETCH-LOGICAL-c550t-56155f43b5a923741b3a07ad05a66ce11595e24bae3711647d51cecfd22072833
container_end_page 363
container_issue 3
container_start_page 347
container_title Cell and tissue research
container_volume 370
creator Johnson Chacko, L.
Blumer, M. J. F.
Pechriggl, E.
Rask-Andersen, H.
Dietl, W.
Haim, A.
Fritsch, H.
Glueckert, R.
Dudas, J.
Schrott-Fischer, A.
description The expression patterns of the neurotrophin, brain-derived neurotrophic factor, BDNF, and the neurotrophic receptors—p75NTR and Trk receptors—in the developing human fetal inner ear between the gestational weeks (GW) 9 to 12 are examined via in situ hybridization and immunohistochemistry. BDNF mRNA expression was highest in the cochlea at GW 9 but declined in the course of development. In contrast to embryonic murine specimens, a decline in BDNF expression from the apical to the basal turn of the cochlea could not be observed. p75NTR immunostaining was most prominent in the nerve fibers that penetrate into the sensory epithelia of the cochlea, the urticule and the saccule as gestational age progresses. TrkB and TrkC expression intensified towards GW 12, at which point the BDNF mRNA localization was at its lowest. TrkA expression was limited to fiber subpopulations of the facial nerve at GW 10. In the adult human inner ear, we observed BDNF mRNA expression in the apical poles of the cochlear hair cells and supporting cells, while in the adult human utricle, the expression was localized in the vestibular hair cells. We demonstrate the highly specific staining patterns of BDNF mRNA and its putative receptors over a developmental period in which multiple hearing disorders are manifested. Our findings suggest that BDNF and neurotrophin receptors are important players during early human inner ear development. In particular, they seem to be important for the survival of the afferent sensory neurons.
doi_str_mv 10.1007/s00441-017-2686-9
format article
fullrecord <record><control><sourceid>gale_swepu</sourceid><recordid>TN_cdi_swepub_primary_oai_DiVA_org_uu_343574</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A516023198</galeid><sourcerecordid>A516023198</sourcerecordid><originalsourceid>FETCH-LOGICAL-c550t-56155f43b5a923741b3a07ad05a66ce11595e24bae3711647d51cecfd22072833</originalsourceid><addsrcrecordid>eNp1kl-L1DAUxYso7rj6AXyRgiA-2DU3f9vHcddRYVEQFd9Cmt7OdGmTmjSK394MM667ouQhIfmdG87hFMVjIGdAiHoZCeEcKgKqorKWVXOnWAFntCK1qu8WK8IIrZSUX0-KBzFeEQJcyuZ-cULrhvJawqrYfPQjlr4vX12835TGdaXDFPwS_LwbbBnQ4rz4EMvBlbs0GZcPDkOJJpQdfsfRzxO65WFxrzdjxEfH_bT4vHn96fxtdfnhzbvz9WVlhSBLJSQI0XPWCtNQpji0zBBlOiKMlBYBRCOQ8tYgUwCSq06ARdt3lBJFa8ZOixeHufEHzqnVcxgmE35qbwZ9MXxZax-2OiXNOBOKZ_z5AZ-D_5YwLnoaosVxNA59ihoaTvKXtYCMPv0LvfIpuGwmU7JuOJBa_qG2ZkQ9uD4nZex-qF4LkIQyaOpMnf2DyqvDabDeYT_k-1uCZzcEOzTjsot-TMvgXbwNwgG0wccYsL9OAIjed0IfOqFzJ_S-E7rJmidHZ6mdsLtW_C5BBugx1PzkthhuWP_v1F-bi7yV</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1968941086</pqid></control><display><type>article</type><title>Role of BDNF and neurotrophic receptors in human inner ear development</title><source>Springer Nature</source><creator>Johnson Chacko, L. ; Blumer, M. J. F. ; Pechriggl, E. ; Rask-Andersen, H. ; Dietl, W. ; Haim, A. ; Fritsch, H. ; Glueckert, R. ; Dudas, J. ; Schrott-Fischer, A.</creator><creatorcontrib>Johnson Chacko, L. ; Blumer, M. J. F. ; Pechriggl, E. ; Rask-Andersen, H. ; Dietl, W. ; Haim, A. ; Fritsch, H. ; Glueckert, R. ; Dudas, J. ; Schrott-Fischer, A.</creatorcontrib><description>The expression patterns of the neurotrophin, brain-derived neurotrophic factor, BDNF, and the neurotrophic receptors—p75NTR and Trk receptors—in the developing human fetal inner ear between the gestational weeks (GW) 9 to 12 are examined via in situ hybridization and immunohistochemistry. BDNF mRNA expression was highest in the cochlea at GW 9 but declined in the course of development. In contrast to embryonic murine specimens, a decline in BDNF expression from the apical to the basal turn of the cochlea could not be observed. p75NTR immunostaining was most prominent in the nerve fibers that penetrate into the sensory epithelia of the cochlea, the urticule and the saccule as gestational age progresses. TrkB and TrkC expression intensified towards GW 12, at which point the BDNF mRNA localization was at its lowest. TrkA expression was limited to fiber subpopulations of the facial nerve at GW 10. In the adult human inner ear, we observed BDNF mRNA expression in the apical poles of the cochlear hair cells and supporting cells, while in the adult human utricle, the expression was localized in the vestibular hair cells. We demonstrate the highly specific staining patterns of BDNF mRNA and its putative receptors over a developmental period in which multiple hearing disorders are manifested. Our findings suggest that BDNF and neurotrophin receptors are important players during early human inner ear development. In particular, they seem to be important for the survival of the afferent sensory neurons.</description><identifier>ISSN: 0302-766X</identifier><identifier>ISSN: 1432-0878</identifier><identifier>EISSN: 1432-0878</identifier><identifier>DOI: 10.1007/s00441-017-2686-9</identifier><identifier>PMID: 28924861</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Animals ; Base Sequence ; BDNF ; Biomedical and Life Sciences ; Biomedicine ; Brain-derived neurotrophic factor ; Brain-Derived Neurotrophic Factor - metabolism ; Cochlea ; Cochlea - embryology ; Cochlea - metabolism ; Embryogenesis ; Facial nerve ; Fetuses ; Fibers ; Gene expression ; Gene Expression Regulation, Developmental ; Gestational age ; Hair ; Hair cells ; Hearing protection ; Human ; Human Genetics ; Humans ; Immunohistochemistry ; In situ hybridization ; Inner ear ; Localization ; Membrane Glycoproteins - metabolism ; Mice ; Molecular Medicine ; Nerve Growth Factors - metabolism ; Nerve Tissue Proteins - metabolism ; Neurons ; Neurotrophin receptors ; Proteomics ; Receptor, trkA - metabolism ; Receptor, trkB - metabolism ; Receptor, trkC - metabolism ; Receptors, Nerve Growth Factor - metabolism ; Regular Article ; RNA ; Saccule ; Sensory neurons ; Subpopulations ; Trk receptors ; TrkA protein ; TrkA receptors ; TrkB receptors ; Utricle ; Vestibular system</subject><ispartof>Cell and tissue research, 2017-12, Vol.370 (3), p.347-363</ispartof><rights>The Author(s) 2017</rights><rights>COPYRIGHT 2017 Springer</rights><rights>Cell and Tissue Research is a copyright of Springer, (2017). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c550t-56155f43b5a923741b3a07ad05a66ce11595e24bae3711647d51cecfd22072833</citedby><cites>FETCH-LOGICAL-c550t-56155f43b5a923741b3a07ad05a66ce11595e24bae3711647d51cecfd22072833</cites><orcidid>0000-0002-4514-9867</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28924861$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-343574$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Johnson Chacko, L.</creatorcontrib><creatorcontrib>Blumer, M. J. F.</creatorcontrib><creatorcontrib>Pechriggl, E.</creatorcontrib><creatorcontrib>Rask-Andersen, H.</creatorcontrib><creatorcontrib>Dietl, W.</creatorcontrib><creatorcontrib>Haim, A.</creatorcontrib><creatorcontrib>Fritsch, H.</creatorcontrib><creatorcontrib>Glueckert, R.</creatorcontrib><creatorcontrib>Dudas, J.</creatorcontrib><creatorcontrib>Schrott-Fischer, A.</creatorcontrib><title>Role of BDNF and neurotrophic receptors in human inner ear development</title><title>Cell and tissue research</title><addtitle>Cell Tissue Res</addtitle><addtitle>Cell Tissue Res</addtitle><description>The expression patterns of the neurotrophin, brain-derived neurotrophic factor, BDNF, and the neurotrophic receptors—p75NTR and Trk receptors—in the developing human fetal inner ear between the gestational weeks (GW) 9 to 12 are examined via in situ hybridization and immunohistochemistry. BDNF mRNA expression was highest in the cochlea at GW 9 but declined in the course of development. In contrast to embryonic murine specimens, a decline in BDNF expression from the apical to the basal turn of the cochlea could not be observed. p75NTR immunostaining was most prominent in the nerve fibers that penetrate into the sensory epithelia of the cochlea, the urticule and the saccule as gestational age progresses. TrkB and TrkC expression intensified towards GW 12, at which point the BDNF mRNA localization was at its lowest. TrkA expression was limited to fiber subpopulations of the facial nerve at GW 10. In the adult human inner ear, we observed BDNF mRNA expression in the apical poles of the cochlear hair cells and supporting cells, while in the adult human utricle, the expression was localized in the vestibular hair cells. We demonstrate the highly specific staining patterns of BDNF mRNA and its putative receptors over a developmental period in which multiple hearing disorders are manifested. Our findings suggest that BDNF and neurotrophin receptors are important players during early human inner ear development. In particular, they seem to be important for the survival of the afferent sensory neurons.</description><subject>Animals</subject><subject>Base Sequence</subject><subject>BDNF</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain-derived neurotrophic factor</subject><subject>Brain-Derived Neurotrophic Factor - metabolism</subject><subject>Cochlea</subject><subject>Cochlea - embryology</subject><subject>Cochlea - metabolism</subject><subject>Embryogenesis</subject><subject>Facial nerve</subject><subject>Fetuses</subject><subject>Fibers</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Developmental</subject><subject>Gestational age</subject><subject>Hair</subject><subject>Hair cells</subject><subject>Hearing protection</subject><subject>Human</subject><subject>Human Genetics</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>In situ hybridization</subject><subject>Inner ear</subject><subject>Localization</subject><subject>Membrane Glycoproteins - metabolism</subject><subject>Mice</subject><subject>Molecular Medicine</subject><subject>Nerve Growth Factors - metabolism</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Neurons</subject><subject>Neurotrophin receptors</subject><subject>Proteomics</subject><subject>Receptor, trkA - metabolism</subject><subject>Receptor, trkB - metabolism</subject><subject>Receptor, trkC - metabolism</subject><subject>Receptors, Nerve Growth Factor - metabolism</subject><subject>Regular Article</subject><subject>RNA</subject><subject>Saccule</subject><subject>Sensory neurons</subject><subject>Subpopulations</subject><subject>Trk receptors</subject><subject>TrkA protein</subject><subject>TrkA receptors</subject><subject>TrkB receptors</subject><subject>Utricle</subject><subject>Vestibular system</subject><issn>0302-766X</issn><issn>1432-0878</issn><issn>1432-0878</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp1kl-L1DAUxYso7rj6AXyRgiA-2DU3f9vHcddRYVEQFd9Cmt7OdGmTmjSK394MM667ouQhIfmdG87hFMVjIGdAiHoZCeEcKgKqorKWVXOnWAFntCK1qu8WK8IIrZSUX0-KBzFeEQJcyuZ-cULrhvJawqrYfPQjlr4vX12835TGdaXDFPwS_LwbbBnQ4rz4EMvBlbs0GZcPDkOJJpQdfsfRzxO65WFxrzdjxEfH_bT4vHn96fxtdfnhzbvz9WVlhSBLJSQI0XPWCtNQpji0zBBlOiKMlBYBRCOQ8tYgUwCSq06ARdt3lBJFa8ZOixeHufEHzqnVcxgmE35qbwZ9MXxZax-2OiXNOBOKZ_z5AZ-D_5YwLnoaosVxNA59ihoaTvKXtYCMPv0LvfIpuGwmU7JuOJBa_qG2ZkQ9uD4nZex-qF4LkIQyaOpMnf2DyqvDabDeYT_k-1uCZzcEOzTjsot-TMvgXbwNwgG0wccYsL9OAIjed0IfOqFzJ_S-E7rJmidHZ6mdsLtW_C5BBugx1PzkthhuWP_v1F-bi7yV</recordid><startdate>20171201</startdate><enddate>20171201</enddate><creator>Johnson Chacko, L.</creator><creator>Blumer, M. J. F.</creator><creator>Pechriggl, E.</creator><creator>Rask-Andersen, H.</creator><creator>Dietl, W.</creator><creator>Haim, A.</creator><creator>Fritsch, H.</creator><creator>Glueckert, R.</creator><creator>Dudas, J.</creator><creator>Schrott-Fischer, A.</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><scope>C6C</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>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7SS</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>ACNBI</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>DF2</scope><scope>ZZAVC</scope><orcidid>https://orcid.org/0000-0002-4514-9867</orcidid></search><sort><creationdate>20171201</creationdate><title>Role of BDNF and neurotrophic receptors in human inner ear development</title><author>Johnson Chacko, L. ; Blumer, M. J. F. ; Pechriggl, E. ; Rask-Andersen, H. ; Dietl, W. ; Haim, A. ; Fritsch, H. ; Glueckert, R. ; Dudas, J. ; Schrott-Fischer, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c550t-56155f43b5a923741b3a07ad05a66ce11595e24bae3711647d51cecfd22072833</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Base Sequence</topic><topic>BDNF</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brain-derived neurotrophic factor</topic><topic>Brain-Derived Neurotrophic Factor - metabolism</topic><topic>Cochlea</topic><topic>Cochlea - embryology</topic><topic>Cochlea - metabolism</topic><topic>Embryogenesis</topic><topic>Facial nerve</topic><topic>Fetuses</topic><topic>Fibers</topic><topic>Gene expression</topic><topic>Gene Expression Regulation, Developmental</topic><topic>Gestational age</topic><topic>Hair</topic><topic>Hair cells</topic><topic>Hearing protection</topic><topic>Human</topic><topic>Human Genetics</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>In situ hybridization</topic><topic>Inner ear</topic><topic>Localization</topic><topic>Membrane Glycoproteins - metabolism</topic><topic>Mice</topic><topic>Molecular Medicine</topic><topic>Nerve Growth Factors - metabolism</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Neurons</topic><topic>Neurotrophin receptors</topic><topic>Proteomics</topic><topic>Receptor, trkA - metabolism</topic><topic>Receptor, trkB - metabolism</topic><topic>Receptor, trkC - metabolism</topic><topic>Receptors, Nerve Growth Factor - metabolism</topic><topic>Regular Article</topic><topic>RNA</topic><topic>Saccule</topic><topic>Sensory neurons</topic><topic>Subpopulations</topic><topic>Trk receptors</topic><topic>TrkA protein</topic><topic>TrkA receptors</topic><topic>TrkB receptors</topic><topic>Utricle</topic><topic>Vestibular system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Johnson Chacko, L.</creatorcontrib><creatorcontrib>Blumer, M. J. F.</creatorcontrib><creatorcontrib>Pechriggl, E.</creatorcontrib><creatorcontrib>Rask-Andersen, H.</creatorcontrib><creatorcontrib>Dietl, W.</creatorcontrib><creatorcontrib>Haim, A.</creatorcontrib><creatorcontrib>Fritsch, H.</creatorcontrib><creatorcontrib>Glueckert, R.</creatorcontrib><creatorcontrib>Dudas, J.</creatorcontrib><creatorcontrib>Schrott-Fischer, A.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nursing &amp; Allied Health Database (ProQuest)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Biological Science Journals</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>SWEPUB Uppsala universitet full text</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Uppsala universitet</collection><collection>SwePub Articles full text</collection><jtitle>Cell and tissue research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Johnson Chacko, L.</au><au>Blumer, M. J. F.</au><au>Pechriggl, E.</au><au>Rask-Andersen, H.</au><au>Dietl, W.</au><au>Haim, A.</au><au>Fritsch, H.</au><au>Glueckert, R.</au><au>Dudas, J.</au><au>Schrott-Fischer, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of BDNF and neurotrophic receptors in human inner ear development</atitle><jtitle>Cell and tissue research</jtitle><stitle>Cell Tissue Res</stitle><addtitle>Cell Tissue Res</addtitle><date>2017-12-01</date><risdate>2017</risdate><volume>370</volume><issue>3</issue><spage>347</spage><epage>363</epage><pages>347-363</pages><issn>0302-766X</issn><issn>1432-0878</issn><eissn>1432-0878</eissn><abstract>The expression patterns of the neurotrophin, brain-derived neurotrophic factor, BDNF, and the neurotrophic receptors—p75NTR and Trk receptors—in the developing human fetal inner ear between the gestational weeks (GW) 9 to 12 are examined via in situ hybridization and immunohistochemistry. BDNF mRNA expression was highest in the cochlea at GW 9 but declined in the course of development. In contrast to embryonic murine specimens, a decline in BDNF expression from the apical to the basal turn of the cochlea could not be observed. p75NTR immunostaining was most prominent in the nerve fibers that penetrate into the sensory epithelia of the cochlea, the urticule and the saccule as gestational age progresses. TrkB and TrkC expression intensified towards GW 12, at which point the BDNF mRNA localization was at its lowest. TrkA expression was limited to fiber subpopulations of the facial nerve at GW 10. In the adult human inner ear, we observed BDNF mRNA expression in the apical poles of the cochlear hair cells and supporting cells, while in the adult human utricle, the expression was localized in the vestibular hair cells. We demonstrate the highly specific staining patterns of BDNF mRNA and its putative receptors over a developmental period in which multiple hearing disorders are manifested. Our findings suggest that BDNF and neurotrophin receptors are important players during early human inner ear development. In particular, they seem to be important for the survival of the afferent sensory neurons.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>28924861</pmid><doi>10.1007/s00441-017-2686-9</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0002-4514-9867</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0302-766X
ispartof Cell and tissue research, 2017-12, Vol.370 (3), p.347-363
issn 0302-766X
1432-0878
1432-0878
language eng
recordid cdi_swepub_primary_oai_DiVA_org_uu_343574
source Springer Nature
subjects Animals
Base Sequence
BDNF
Biomedical and Life Sciences
Biomedicine
Brain-derived neurotrophic factor
Brain-Derived Neurotrophic Factor - metabolism
Cochlea
Cochlea - embryology
Cochlea - metabolism
Embryogenesis
Facial nerve
Fetuses
Fibers
Gene expression
Gene Expression Regulation, Developmental
Gestational age
Hair
Hair cells
Hearing protection
Human
Human Genetics
Humans
Immunohistochemistry
In situ hybridization
Inner ear
Localization
Membrane Glycoproteins - metabolism
Mice
Molecular Medicine
Nerve Growth Factors - metabolism
Nerve Tissue Proteins - metabolism
Neurons
Neurotrophin receptors
Proteomics
Receptor, trkA - metabolism
Receptor, trkB - metabolism
Receptor, trkC - metabolism
Receptors, Nerve Growth Factor - metabolism
Regular Article
RNA
Saccule
Sensory neurons
Subpopulations
Trk receptors
TrkA protein
TrkA receptors
TrkB receptors
Utricle
Vestibular system
title Role of BDNF and neurotrophic receptors in human inner ear development
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T13%3A20%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_swepu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Role%20of%20BDNF%20and%20neurotrophic%20receptors%20in%20human%20inner%20ear%20development&rft.jtitle=Cell%20and%20tissue%20research&rft.au=Johnson%20Chacko,%20L.&rft.date=2017-12-01&rft.volume=370&rft.issue=3&rft.spage=347&rft.epage=363&rft.pages=347-363&rft.issn=0302-766X&rft.eissn=1432-0878&rft_id=info:doi/10.1007/s00441-017-2686-9&rft_dat=%3Cgale_swepu%3EA516023198%3C/gale_swepu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c550t-56155f43b5a923741b3a07ad05a66ce11595e24bae3711647d51cecfd22072833%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1968941086&rft_id=info:pmid/28924861&rft_galeid=A516023198&rfr_iscdi=true