Expression of Collagens in the Otosclerotic Bone
The etiopathogenesis of otosclerosis is still controversially discussed. The major hypotheses discussed are a viral infection on a genetic background and an (autoimmune) collagen disease. The aim of our study was to investigate by immunohistochemistry the expression pattern of collagens within the o...
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description | The etiopathogenesis of otosclerosis is still controversially discussed. The major hypotheses discussed are a viral infection on a genetic background and an (autoimmune) collagen disease. The aim of our study was to investigate by immunohistochemistry the expression pattern of collagens within the otosclerotic focus. Stapes footplates from 30 patients with clinical otosclerosis undergoing stapedectomy were formalin fixed, decalcified and paraffin embedded. As controls, 30 autoptic temporal bone specimens were employed. We investigated the expression of collagens I-V with immunohistochemistry. The expression of collagen I showed a diffuse homogeneous distribution with increased staining of the otosclerotic focus. Collagen II was exclusively expressed in chondrocytes including the globuli interossei. The pattern of collagen III in the otosclerotic bone was web-like in contrast to a lamellar pattern in the control bone. The mucoperiosteal layer and connective tissue such as the vessels of the resorption lacunae expressed collagen IV. An increased expression of collagen V around osteocytes was observed in the otosclerotic focus. In conclusion, in the otosclerotic tissue, in comparison with the control bone, a high expression of collagen IV occurred. The immunohistochemical analysis of collagen II, which has been suggested to be implicated in the etiopathogenesis of otosclerosis, revealed no differences between control and otosclerotic bones. The intense staining of the otosclerotic focus with collagen I is in good agreement with an inflammatory process but in contrast with lesions like those in osteogenesis imperfecta. |
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The major hypotheses discussed are a viral infection on a genetic background and an (autoimmune) collagen disease. The aim of our study was to investigate by immunohistochemistry the expression pattern of collagens within the otosclerotic focus. Stapes footplates from 30 patients with clinical otosclerosis undergoing stapedectomy were formalin fixed, decalcified and paraffin embedded. As controls, 30 autoptic temporal bone specimens were employed. We investigated the expression of collagens I-V with immunohistochemistry. The expression of collagen I showed a diffuse homogeneous distribution with increased staining of the otosclerotic focus. Collagen II was exclusively expressed in chondrocytes including the globuli interossei. The pattern of collagen III in the otosclerotic bone was web-like in contrast to a lamellar pattern in the control bone. The mucoperiosteal layer and connective tissue such as the vessels of the resorption lacunae expressed collagen IV. An increased expression of collagen V around osteocytes was observed in the otosclerotic focus. In conclusion, in the otosclerotic tissue, in comparison with the control bone, a high expression of collagen IV occurred. The immunohistochemical analysis of collagen II, which has been suggested to be implicated in the etiopathogenesis of otosclerosis, revealed no differences between control and otosclerotic bones. The intense staining of the otosclerotic focus with collagen I is in good agreement with an inflammatory process but in contrast with lesions like those in osteogenesis imperfecta.</description><identifier>ISSN: 0065-3071</identifier><identifier>ISBN: 3805581130</identifier><identifier>ISBN: 9783805581134</identifier><identifier>EISSN: 1662-2847</identifier><identifier>EISBN: 9783318013436</identifier><identifier>EISBN: 3318013439</identifier><identifier>DOI: 10.1159/000098668</identifier><identifier>PMID: 17245021</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Adult ; Chapter ; Chondrocytes - pathology ; Collagen - genetics ; Collagen Type I - genetics ; Collagen Type II - genetics ; Collagen Type III - genetics ; Collagen Type IV - genetics ; Connective Tissue - pathology ; Female ; Humans ; Immunoenzyme Techniques ; Male ; Middle Aged ; Otosclerosis - genetics ; Otosclerosis - pathology ; Periosteum - pathology ; Stapes - pathology ; Temporal Bone - pathology</subject><ispartof>Advances in Oto-Rhino-Laryngology, 2007-01, Vol.65, p.45-49</ispartof><rights>2007 S. 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The major hypotheses discussed are a viral infection on a genetic background and an (autoimmune) collagen disease. The aim of our study was to investigate by immunohistochemistry the expression pattern of collagens within the otosclerotic focus. Stapes footplates from 30 patients with clinical otosclerosis undergoing stapedectomy were formalin fixed, decalcified and paraffin embedded. As controls, 30 autoptic temporal bone specimens were employed. We investigated the expression of collagens I-V with immunohistochemistry. The expression of collagen I showed a diffuse homogeneous distribution with increased staining of the otosclerotic focus. Collagen II was exclusively expressed in chondrocytes including the globuli interossei. The pattern of collagen III in the otosclerotic bone was web-like in contrast to a lamellar pattern in the control bone. The mucoperiosteal layer and connective tissue such as the vessels of the resorption lacunae expressed collagen IV. An increased expression of collagen V around osteocytes was observed in the otosclerotic focus. In conclusion, in the otosclerotic tissue, in comparison with the control bone, a high expression of collagen IV occurred. The immunohistochemical analysis of collagen II, which has been suggested to be implicated in the etiopathogenesis of otosclerosis, revealed no differences between control and otosclerotic bones. The intense staining of the otosclerotic focus with collagen I is in good agreement with an inflammatory process but in contrast with lesions like those in osteogenesis imperfecta.</description><subject>Adult</subject><subject>Chapter</subject><subject>Chondrocytes - pathology</subject><subject>Collagen - genetics</subject><subject>Collagen Type I - genetics</subject><subject>Collagen Type II - genetics</subject><subject>Collagen Type III - genetics</subject><subject>Collagen Type IV - genetics</subject><subject>Connective Tissue - pathology</subject><subject>Female</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Otosclerosis - genetics</subject><subject>Otosclerosis - pathology</subject><subject>Periosteum - pathology</subject><subject>Stapes - pathology</subject><subject>Temporal Bone - pathology</subject><issn>0065-3071</issn><issn>1662-2847</issn><isbn>3805581130</isbn><isbn>9783805581134</isbn><isbn>9783318013436</isbn><isbn>3318013439</isbn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0LlOw0AQBuDlEgkhBS-AXCA6w95HCRGXFCkN1NbaOxtMHK_ZdSR4ewwJdaYZjfTp1-hH6ILgG0KEucXDGC2lPkBTozRjRGPCOJOHaEykpDnVXB2hM6axEJoQho_RGGMpcoYVGaFpSh-_GZRIReUpGhFFuRjOMcIPX12ElOrQZsFns9A0dgltyuo2698hW_QhVQ3E0NdVdh9aOEcn3jYJprs9QW-PD6-z53y-eHqZ3c3zFcWmz6WVynDhLUhXGVpii0tGiKu0csxrh7lXwihrAbxgrhLae66l46ZyRoiSTdD1NreL4XMDqS_WdapgeK-FsEmF1IYTrPBeSIc-BONigJc7uCnX4Iou1msbv4v_MgaQbcHKxiXEAsoQVilBrCEVf_0P5GoPKTrn2Q-n43xM</recordid><startdate>200701</startdate><enddate>200701</enddate><creator>Niedermeyer, H.P.</creator><creator>Becker, E.T.</creator><creator>Arnold, W.</creator><general>S. Karger AG</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QP</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope><scope>8BM</scope></search><sort><creationdate>200701</creationdate><title>Expression of Collagens in the Otosclerotic Bone</title><author>Niedermeyer, H.P. ; Becker, E.T. ; Arnold, W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-k209t-6a67945fae6dc92b0a0b311dc87d3f8d04f7597aaeef53dc58ff486d49cd955b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Chapter</topic><topic>Chondrocytes - pathology</topic><topic>Collagen - genetics</topic><topic>Collagen Type I - genetics</topic><topic>Collagen Type II - genetics</topic><topic>Collagen Type III - genetics</topic><topic>Collagen Type IV - genetics</topic><topic>Connective Tissue - pathology</topic><topic>Female</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Otosclerosis - genetics</topic><topic>Otosclerosis - pathology</topic><topic>Periosteum - pathology</topic><topic>Stapes - pathology</topic><topic>Temporal Bone - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Niedermeyer, H.P.</creatorcontrib><creatorcontrib>Becker, E.T.</creatorcontrib><creatorcontrib>Arnold, W.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>ComDisDome</collection><jtitle>Advances in Oto-Rhino-Laryngology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Niedermeyer, H.P.</au><au>Becker, E.T.</au><au>Arnold, W.</au><au>Häusler R</au><au>Arnold W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of Collagens in the Otosclerotic Bone</atitle><jtitle>Advances in Oto-Rhino-Laryngology</jtitle><addtitle>Adv Otorhinolaryngol</addtitle><date>2007-01</date><risdate>2007</risdate><volume>65</volume><spage>45</spage><epage>49</epage><pages>45-49</pages><issn>0065-3071</issn><eissn>1662-2847</eissn><isbn>3805581130</isbn><isbn>9783805581134</isbn><eisbn>9783318013436</eisbn><eisbn>3318013439</eisbn><abstract>The etiopathogenesis of otosclerosis is still controversially discussed. The major hypotheses discussed are a viral infection on a genetic background and an (autoimmune) collagen disease. The aim of our study was to investigate by immunohistochemistry the expression pattern of collagens within the otosclerotic focus. Stapes footplates from 30 patients with clinical otosclerosis undergoing stapedectomy were formalin fixed, decalcified and paraffin embedded. As controls, 30 autoptic temporal bone specimens were employed. We investigated the expression of collagens I-V with immunohistochemistry. The expression of collagen I showed a diffuse homogeneous distribution with increased staining of the otosclerotic focus. Collagen II was exclusively expressed in chondrocytes including the globuli interossei. The pattern of collagen III in the otosclerotic bone was web-like in contrast to a lamellar pattern in the control bone. The mucoperiosteal layer and connective tissue such as the vessels of the resorption lacunae expressed collagen IV. An increased expression of collagen V around osteocytes was observed in the otosclerotic focus. In conclusion, in the otosclerotic tissue, in comparison with the control bone, a high expression of collagen IV occurred. The immunohistochemical analysis of collagen II, which has been suggested to be implicated in the etiopathogenesis of otosclerosis, revealed no differences between control and otosclerotic bones. The intense staining of the otosclerotic focus with collagen I is in good agreement with an inflammatory process but in contrast with lesions like those in osteogenesis imperfecta.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>17245021</pmid><doi>10.1159/000098668</doi><tpages>5</tpages></addata></record> |
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subjects | Adult Chapter Chondrocytes - pathology Collagen - genetics Collagen Type I - genetics Collagen Type II - genetics Collagen Type III - genetics Collagen Type IV - genetics Connective Tissue - pathology Female Humans Immunoenzyme Techniques Male Middle Aged Otosclerosis - genetics Otosclerosis - pathology Periosteum - pathology Stapes - pathology Temporal Bone - pathology |
title | Expression of Collagens in the Otosclerotic Bone |
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