Detection of Otosclerosis-Specific Measles Virus Receptor (Cd46) Protein Isoforms
Genetic predisposition of otosclerosis has long been suspected, but unclarified. Unique coexpression pattern of measles virus receptor (CD46) splicing isoforms in the human otic capsule is assumed, since otosclerosis is a measles virus-associated organ-specific disease. In order to identify CD46 inv...
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Veröffentlicht in: | ISRN otolaryngology 2013-06, Vol.2013, p.479482-6 |
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description | Genetic predisposition of otosclerosis has long been suspected, but unclarified. Unique coexpression pattern of measles virus receptor (CD46) splicing isoforms in the human otic capsule is assumed, since otosclerosis is a measles virus-associated organ-specific disease. In order to identify CD46 involved in the pathogenesis of otosclerosis, we used representative groups of histologically diagnosed otosclerotic, nonotosclerotic, and normal stapes footplates (n=109). Consecutive histopathological examinations and CD46-specific Western blot analysis were performed. Normal and nonotosclerotic stapes footplates showed consistent expression of the conventional c, d, e, f, and l CD46 isoforms. In contrast, four novel isoforms (os1–4) translated as intact proteins were additionally detected in each otosclerotic specimen. The study herein presented provides evidence for the otosclerosis-associated expression pattern of CD46. This finding might explain the organ-specific, virus-associated and autoimmune-inflammatory pathogenesis of otosclerosis. Regarding our current knowledge, this is the first report that confirms the presence of four new disease-specific protein variants of CD46. |
doi_str_mv | 10.1155/2013/479482 |
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C. ; Just, T. ; Thurnher, D. ; Ishikawa, K.</contributor><creatorcontrib>Liktor, Balázs ; Csomor, Péter ; Karosi, Tamás ; Sone, M. ; Alpini, D. C. ; Just, T. ; Thurnher, D. ; Ishikawa, K.</creatorcontrib><description>Genetic predisposition of otosclerosis has long been suspected, but unclarified. Unique coexpression pattern of measles virus receptor (CD46) splicing isoforms in the human otic capsule is assumed, since otosclerosis is a measles virus-associated organ-specific disease. In order to identify CD46 involved in the pathogenesis of otosclerosis, we used representative groups of histologically diagnosed otosclerotic, nonotosclerotic, and normal stapes footplates (n=109). Consecutive histopathological examinations and CD46-specific Western blot analysis were performed. Normal and nonotosclerotic stapes footplates showed consistent expression of the conventional c, d, e, f, and l CD46 isoforms. In contrast, four novel isoforms (os1–4) translated as intact proteins were additionally detected in each otosclerotic specimen. The study herein presented provides evidence for the otosclerosis-associated expression pattern of CD46. This finding might explain the organ-specific, virus-associated and autoimmune-inflammatory pathogenesis of otosclerosis. Regarding our current knowledge, this is the first report that confirms the presence of four new disease-specific protein variants of CD46.</description><identifier>ISSN: 2090-5742</identifier><identifier>ISSN: 2090-5750</identifier><identifier>EISSN: 2090-5750</identifier><identifier>DOI: 10.1155/2013/479482</identifier><identifier>PMID: 23864959</identifier><language>eng</language><publisher>Egypt: Hindawi Publishing Corporation</publisher><ispartof>ISRN otolaryngology, 2013-06, Vol.2013, p.479482-6</ispartof><rights>Copyright © 2013 Balázs Liktor et al.</rights><rights>Copyright © 2013 Balázs Liktor et al. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2612-c203b7d2990d390d7327749901378d6c6bcdf707112e917b8374323523ced7923</citedby><cites>FETCH-LOGICAL-c2612-c203b7d2990d390d7327749901378d6c6bcdf707112e917b8374323523ced7923</cites><orcidid>0000-0001-6326-7608</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706069/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706069/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23864959$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Sone, M.</contributor><contributor>Alpini, D. 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Consecutive histopathological examinations and CD46-specific Western blot analysis were performed. Normal and nonotosclerotic stapes footplates showed consistent expression of the conventional c, d, e, f, and l CD46 isoforms. In contrast, four novel isoforms (os1–4) translated as intact proteins were additionally detected in each otosclerotic specimen. The study herein presented provides evidence for the otosclerosis-associated expression pattern of CD46. This finding might explain the organ-specific, virus-associated and autoimmune-inflammatory pathogenesis of otosclerosis. 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C.</au><au>Just, T.</au><au>Thurnher, D.</au><au>Ishikawa, K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of Otosclerosis-Specific Measles Virus Receptor (Cd46) Protein Isoforms</atitle><jtitle>ISRN otolaryngology</jtitle><addtitle>ISRN Otolaryngol</addtitle><date>2013-06-20</date><risdate>2013</risdate><volume>2013</volume><spage>479482</spage><epage>6</epage><pages>479482-6</pages><issn>2090-5742</issn><issn>2090-5750</issn><eissn>2090-5750</eissn><abstract>Genetic predisposition of otosclerosis has long been suspected, but unclarified. Unique coexpression pattern of measles virus receptor (CD46) splicing isoforms in the human otic capsule is assumed, since otosclerosis is a measles virus-associated organ-specific disease. In order to identify CD46 involved in the pathogenesis of otosclerosis, we used representative groups of histologically diagnosed otosclerotic, nonotosclerotic, and normal stapes footplates (n=109). Consecutive histopathological examinations and CD46-specific Western blot analysis were performed. Normal and nonotosclerotic stapes footplates showed consistent expression of the conventional c, d, e, f, and l CD46 isoforms. In contrast, four novel isoforms (os1–4) translated as intact proteins were additionally detected in each otosclerotic specimen. The study herein presented provides evidence for the otosclerosis-associated expression pattern of CD46. This finding might explain the organ-specific, virus-associated and autoimmune-inflammatory pathogenesis of otosclerosis. Regarding our current knowledge, this is the first report that confirms the presence of four new disease-specific protein variants of CD46.</abstract><cop>Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>23864959</pmid><doi>10.1155/2013/479482</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-6326-7608</orcidid><oa>free_for_read</oa></addata></record> |
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title | Detection of Otosclerosis-Specific Measles Virus Receptor (Cd46) Protein Isoforms |
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