Macrophages and vimentin in tissues adjacent to megaprostheses and mesh in reconstructive surgeries
In reconstructive surgery using artificial materials after wide resection, soft tissues are usually adjacent to metal surfaces or mesh. The purpose of this study was to provide histological evaluation of the soft tissues adjacent to the metal surfaces of megaprostheses and mesh. Tissues from revisio...
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Veröffentlicht in: | Communicative & integrative biology 2022, Vol.15 (1), p.168-181 |
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description | In reconstructive surgery using artificial materials after wide resection, soft tissues are usually adjacent to metal surfaces or mesh. The purpose of this study was to provide histological evaluation of the soft tissues adjacent to the metal surfaces of megaprostheses and mesh. Tissues from revision surgery of megaprosthesis and from wide resection after recurrent thoracic wall sarcoma were used. Histological analysis was evaluated by hematoxylin/eosin (HE) and Masson's trichrome staining, and by immunohistochemical staining for markers including cluster of differentiation 68 (CD68), vimentin, collagen type and S100A4. Soft tissue adherence to the smooth metal surface of Ti alloy was not observed. On the surface of capsule, CD68- and vimentin-positive cells formed a thin layer. In contrast, soft tissue adherence to a rough-surface cobalt chrome alloy was observed. Capsule was not apparent for this tissue, in which CD68- and vimentin-positive cells were aggregated randomly. In the resected tissues of recurrent chest wall sarcoma, muscles showed connections to connective soft tissues but did not invade to the inside of the mesh. Around the polypropylene mesh, large numbers of CD68- and vimentin-positive cells were seen. On the ePTFE, small numbers of CD68-positive cells were observed, while a larger number of the cells were vimentin positive. High accumulation of S100A4-positive cells was observed at the metal surface and polypropylene surface. Cells were strongly positive for CD68 and vimentin in tissues adjacent to metal and mesh surfaces. Macrophages and vimentin may play important roles in the foreign body reaction to metal and mesh, and so may contribute to encapsulation and fibrosis. |
doi_str_mv | 10.1080/19420889.2022.2101193 |
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The purpose of this study was to provide histological evaluation of the soft tissues adjacent to the metal surfaces of megaprostheses and mesh. Tissues from revision surgery of megaprosthesis and from wide resection after recurrent thoracic wall sarcoma were used. Histological analysis was evaluated by hematoxylin/eosin (HE) and Masson's trichrome staining, and by immunohistochemical staining for markers including cluster of differentiation 68 (CD68), vimentin, collagen type and S100A4. Soft tissue adherence to the smooth metal surface of Ti alloy was not observed. On the surface of capsule, CD68- and vimentin-positive cells formed a thin layer. In contrast, soft tissue adherence to a rough-surface cobalt chrome alloy was observed. Capsule was not apparent for this tissue, in which CD68- and vimentin-positive cells were aggregated randomly. In the resected tissues of recurrent chest wall sarcoma, muscles showed connections to connective soft tissues but did not invade to the inside of the mesh. Around the polypropylene mesh, large numbers of CD68- and vimentin-positive cells were seen. On the ePTFE, small numbers of CD68-positive cells were observed, while a larger number of the cells were vimentin positive. High accumulation of S100A4-positive cells was observed at the metal surface and polypropylene surface. Cells were strongly positive for CD68 and vimentin in tissues adjacent to metal and mesh surfaces. Macrophages and vimentin may play important roles in the foreign body reaction to metal and mesh, and so may contribute to encapsulation and fibrosis.</description><identifier>ISSN: 1942-0889</identifier><identifier>EISSN: 1942-0889</identifier><identifier>DOI: 10.1080/19420889.2022.2101193</identifier><identifier>PMID: 36532655</identifier><language>eng</language><publisher>United States: Taylor & Francis</publisher><subject>CD68 ; Cobalt ; Collagen ; Fibrosis ; macrophage ; Macrophages ; megaprosthesis ; mesh ; Muscles ; Polypropylene ; reconstruction ; Reconstructive surgery ; Research Paper ; S100A4 protein ; Sarcoma ; soft tissue integration ; Soft tissues ; Surgical mesh ; Thorax ; Vimentin</subject><ispartof>Communicative & integrative biology, 2022, Vol.15 (1), p.168-181</ispartof><rights>2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2022</rights><rights>2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.</rights><rights>2022 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This work is licensed under the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 The Author(s). 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The purpose of this study was to provide histological evaluation of the soft tissues adjacent to the metal surfaces of megaprostheses and mesh. Tissues from revision surgery of megaprosthesis and from wide resection after recurrent thoracic wall sarcoma were used. Histological analysis was evaluated by hematoxylin/eosin (HE) and Masson's trichrome staining, and by immunohistochemical staining for markers including cluster of differentiation 68 (CD68), vimentin, collagen type and S100A4. Soft tissue adherence to the smooth metal surface of Ti alloy was not observed. On the surface of capsule, CD68- and vimentin-positive cells formed a thin layer. In contrast, soft tissue adherence to a rough-surface cobalt chrome alloy was observed. Capsule was not apparent for this tissue, in which CD68- and vimentin-positive cells were aggregated randomly. In the resected tissues of recurrent chest wall sarcoma, muscles showed connections to connective soft tissues but did not invade to the inside of the mesh. Around the polypropylene mesh, large numbers of CD68- and vimentin-positive cells were seen. On the ePTFE, small numbers of CD68-positive cells were observed, while a larger number of the cells were vimentin positive. High accumulation of S100A4-positive cells was observed at the metal surface and polypropylene surface. Cells were strongly positive for CD68 and vimentin in tissues adjacent to metal and mesh surfaces. Macrophages and vimentin may play important roles in the foreign body reaction to metal and mesh, and so may contribute to encapsulation and fibrosis.</description><subject>CD68</subject><subject>Cobalt</subject><subject>Collagen</subject><subject>Fibrosis</subject><subject>macrophage</subject><subject>Macrophages</subject><subject>megaprosthesis</subject><subject>mesh</subject><subject>Muscles</subject><subject>Polypropylene</subject><subject>reconstruction</subject><subject>Reconstructive surgery</subject><subject>Research Paper</subject><subject>S100A4 protein</subject><subject>Sarcoma</subject><subject>soft tissue integration</subject><subject>Soft tissues</subject><subject>Surgical mesh</subject><subject>Thorax</subject><subject>Vimentin</subject><issn>1942-0889</issn><issn>1942-0889</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><sourceid>DOA</sourceid><recordid>eNp9Ustu1DAUjRCIlsIngCKxYTOD33Y2iKriUamIDaytG_tmxqMkHuxkUP8eh5lWLQskS7bOPffch09VvaZkTYkh72kjGDGmWTPC2JpRQmnDn1TnC75aAk8fvM-qFznvCFGcUf68OuNKcqakPK_cN3Ap7rewwVzD6OtDGHCcwliXM4Wc5wX3O3AFradYD7iBfYp52mI-pQyYtws9oYtjntLspnDAOs9pgylgflk966DP-Op0X1Q_P3_6cfV1dfP9y_XV5c3KCa35SnkpFJaWTdM2SnDnQZVGQRgthPfYNSAVcNMKNFoRTqThTJbclvhGMuQX1fVR10fY2X0KA6RbGyHYv0BMGwtpCq5Hy4WnqKVpTUeF4G1TSmnQ6MuyuKdt0fpw1NrP7YB-mT5B_0j0cWQMW7uJB9toKSjlReDdSSDFX2WJkx1Cdtj3MGKcs2VaSkO4lgv17T_UXZzTWFZVWGUdigtJCkseWeW_ck7Y3TdDiV0sYe8sYRdL2JMlSt6bh5PcZ915oBA-Hglh7GIa4HdMvbcT3PYxdQlGF7Ll_6_xBxC2xgk</recordid><startdate>2022</startdate><enddate>2022</enddate><creator>Asanuma, Kunihiro</creator><creator>Nakamura, Tomoki</creator><creator>Iino, Takahiro</creator><creator>Hagi, Tomohito</creator><creator>Sudo, Akihiro</creator><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><general>Taylor & Francis Group</general><scope>0YH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>8FD</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>M2O</scope><scope>MBDVC</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-1244-0236</orcidid></search><sort><creationdate>2022</creationdate><title>Macrophages and vimentin in tissues adjacent to megaprostheses and mesh in reconstructive surgeries</title><author>Asanuma, Kunihiro ; Nakamura, Tomoki ; Iino, Takahiro ; Hagi, Tomohito ; Sudo, Akihiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4773-6d546e94289b9643cda6365a48744ddef9a56a38b4e87603058325c47b0d952e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>CD68</topic><topic>Cobalt</topic><topic>Collagen</topic><topic>Fibrosis</topic><topic>macrophage</topic><topic>Macrophages</topic><topic>megaprosthesis</topic><topic>mesh</topic><topic>Muscles</topic><topic>Polypropylene</topic><topic>reconstruction</topic><topic>Reconstructive surgery</topic><topic>Research Paper</topic><topic>S100A4 protein</topic><topic>Sarcoma</topic><topic>soft tissue integration</topic><topic>Soft tissues</topic><topic>Surgical mesh</topic><topic>Thorax</topic><topic>Vimentin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Asanuma, Kunihiro</creatorcontrib><creatorcontrib>Nakamura, Tomoki</creatorcontrib><creatorcontrib>Iino, Takahiro</creatorcontrib><creatorcontrib>Hagi, Tomohito</creatorcontrib><creatorcontrib>Sudo, Akihiro</creatorcontrib><collection>Taylor & Francis Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Technology Research Database</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</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>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Communicative & integrative biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Asanuma, Kunihiro</au><au>Nakamura, Tomoki</au><au>Iino, Takahiro</au><au>Hagi, Tomohito</au><au>Sudo, Akihiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Macrophages and vimentin in tissues adjacent to megaprostheses and mesh in reconstructive surgeries</atitle><jtitle>Communicative & integrative biology</jtitle><addtitle>Commun Integr Biol</addtitle><date>2022</date><risdate>2022</risdate><volume>15</volume><issue>1</issue><spage>168</spage><epage>181</epage><pages>168-181</pages><issn>1942-0889</issn><eissn>1942-0889</eissn><abstract>In reconstructive surgery using artificial materials after wide resection, soft tissues are usually adjacent to metal surfaces or mesh. The purpose of this study was to provide histological evaluation of the soft tissues adjacent to the metal surfaces of megaprostheses and mesh. Tissues from revision surgery of megaprosthesis and from wide resection after recurrent thoracic wall sarcoma were used. Histological analysis was evaluated by hematoxylin/eosin (HE) and Masson's trichrome staining, and by immunohistochemical staining for markers including cluster of differentiation 68 (CD68), vimentin, collagen type and S100A4. Soft tissue adherence to the smooth metal surface of Ti alloy was not observed. On the surface of capsule, CD68- and vimentin-positive cells formed a thin layer. In contrast, soft tissue adherence to a rough-surface cobalt chrome alloy was observed. Capsule was not apparent for this tissue, in which CD68- and vimentin-positive cells were aggregated randomly. In the resected tissues of recurrent chest wall sarcoma, muscles showed connections to connective soft tissues but did not invade to the inside of the mesh. Around the polypropylene mesh, large numbers of CD68- and vimentin-positive cells were seen. On the ePTFE, small numbers of CD68-positive cells were observed, while a larger number of the cells were vimentin positive. High accumulation of S100A4-positive cells was observed at the metal surface and polypropylene surface. Cells were strongly positive for CD68 and vimentin in tissues adjacent to metal and mesh surfaces. Macrophages and vimentin may play important roles in the foreign body reaction to metal and mesh, and so may contribute to encapsulation and fibrosis.</abstract><cop>United States</cop><pub>Taylor & Francis</pub><pmid>36532655</pmid><doi>10.1080/19420889.2022.2101193</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-1244-0236</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | CD68 Cobalt Collagen Fibrosis macrophage Macrophages megaprosthesis mesh Muscles Polypropylene reconstruction Reconstructive surgery Research Paper S100A4 protein Sarcoma soft tissue integration Soft tissues Surgical mesh Thorax Vimentin |
title | Macrophages and vimentin in tissues adjacent to megaprostheses and mesh in reconstructive surgeries |
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