Neointimal Formation by Circulating Bone Marrow Cells
: The origin of smooth muscle cells involved in vascular healing was examined. Eighteen C57BL/6 (Ly 5.2) female mice underwent whole body irradiation followed by transfusion with 106 bone nucleated marrow cells from congenic (Ly 5.1) male donors. Successful repopulation by donor marrow was demonstra...
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Veröffentlicht in: | Annals of the New York Academy of Sciences 2001-12, Vol.947 (1), p.18-25 |
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creator | CAMPBELL, JULIE H. HAN, CHIH-LU CAMPBELL, GORDON R. |
description | : The origin of smooth muscle cells involved in vascular healing was examined. Eighteen C57BL/6 (Ly 5.2) female mice underwent whole body irradiation followed by transfusion with 106 bone nucleated marrow cells from congenic (Ly 5.1) male donors. Successful repopulation by donor marrow was demonstrated after 4 weeks by flow cytometry with FITC‐conjugated A20.1/Ly 5.1 monoclonal antibody. The iliac artery of six of the chimeric mice was scratch‐injured by five passes of a probe, causing severe medial damage. After 4 weeks the arterial lumen was obliterated by a cell‐rich neointima, with α‐smooth muscle actin‐containing cells present around the residual lumen. Approximately half of these cells were of male donor origin, as evidenced by in situ hybridization with a Y chromosome‐specific probe. An organized arterial thrombus was formed in the remaining 12 chimeric mice by inserting an 8‐0 silk suture into the left common carotid artery. Donor cells staining with α‐smooth muscle actin were found in those arteries sustaining serious damage but not in arteries with minimal damage. Our results suggest that bone marrow‐derived cells are recruited in vascular healing as a complementary source of smooth muscle‐like cells when the media is severely damaged and few resident smooth muscle cells are available to effect repair. |
doi_str_mv | 10.1111/j.1749-6632.2001.tb03926.x |
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Eighteen C57BL/6 (Ly 5.2) female mice underwent whole body irradiation followed by transfusion with 106 bone nucleated marrow cells from congenic (Ly 5.1) male donors. Successful repopulation by donor marrow was demonstrated after 4 weeks by flow cytometry with FITC‐conjugated A20.1/Ly 5.1 monoclonal antibody. The iliac artery of six of the chimeric mice was scratch‐injured by five passes of a probe, causing severe medial damage. After 4 weeks the arterial lumen was obliterated by a cell‐rich neointima, with α‐smooth muscle actin‐containing cells present around the residual lumen. Approximately half of these cells were of male donor origin, as evidenced by in situ hybridization with a Y chromosome‐specific probe. An organized arterial thrombus was formed in the remaining 12 chimeric mice by inserting an 8‐0 silk suture into the left common carotid artery. Donor cells staining with α‐smooth muscle actin were found in those arteries sustaining serious damage but not in arteries with minimal damage. Our results suggest that bone marrow‐derived cells are recruited in vascular healing as a complementary source of smooth muscle‐like cells when the media is severely damaged and few resident smooth muscle cells are available to effect repair.</description><identifier>ISSN: 0077-8923</identifier><identifier>EISSN: 1749-6632</identifier><identifier>DOI: 10.1111/j.1749-6632.2001.tb03926.x</identifier><identifier>PMID: 11795265</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Arteriosclerosis - pathology ; Arteriosclerosis - physiopathology ; bone marrow cells ; Bone Marrow Cells - cytology ; Bone Marrow Cells - pathology ; Cell Movement ; Humans ; smooth muscle cells ; Tunica Intima - cytology ; Tunica Intima - pathology ; vascular healing ; Wounds and Injuries - pathology ; Wounds and Injuries - physiopathology</subject><ispartof>Annals of the New York Academy of Sciences, 2001-12, Vol.947 (1), p.18-25</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4088-46144069f2396a39836a49da7e1310e87a43eb9f324033a0622afd585ba61d63</citedby><cites>FETCH-LOGICAL-c4088-46144069f2396a39836a49da7e1310e87a43eb9f324033a0622afd585ba61d63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1749-6632.2001.tb03926.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1749-6632.2001.tb03926.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11795265$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CAMPBELL, JULIE H.</creatorcontrib><creatorcontrib>HAN, CHIH-LU</creatorcontrib><creatorcontrib>CAMPBELL, GORDON R.</creatorcontrib><title>Neointimal Formation by Circulating Bone Marrow Cells</title><title>Annals of the New York Academy of Sciences</title><addtitle>Ann N Y Acad Sci</addtitle><description>: The origin of smooth muscle cells involved in vascular healing was examined. Eighteen C57BL/6 (Ly 5.2) female mice underwent whole body irradiation followed by transfusion with 106 bone nucleated marrow cells from congenic (Ly 5.1) male donors. Successful repopulation by donor marrow was demonstrated after 4 weeks by flow cytometry with FITC‐conjugated A20.1/Ly 5.1 monoclonal antibody. The iliac artery of six of the chimeric mice was scratch‐injured by five passes of a probe, causing severe medial damage. After 4 weeks the arterial lumen was obliterated by a cell‐rich neointima, with α‐smooth muscle actin‐containing cells present around the residual lumen. Approximately half of these cells were of male donor origin, as evidenced by in situ hybridization with a Y chromosome‐specific probe. An organized arterial thrombus was formed in the remaining 12 chimeric mice by inserting an 8‐0 silk suture into the left common carotid artery. Donor cells staining with α‐smooth muscle actin were found in those arteries sustaining serious damage but not in arteries with minimal damage. Our results suggest that bone marrow‐derived cells are recruited in vascular healing as a complementary source of smooth muscle‐like cells when the media is severely damaged and few resident smooth muscle cells are available to effect repair.</description><subject>Arteriosclerosis - pathology</subject><subject>Arteriosclerosis - physiopathology</subject><subject>bone marrow cells</subject><subject>Bone Marrow Cells - cytology</subject><subject>Bone Marrow Cells - pathology</subject><subject>Cell Movement</subject><subject>Humans</subject><subject>smooth muscle cells</subject><subject>Tunica Intima - cytology</subject><subject>Tunica Intima - pathology</subject><subject>vascular healing</subject><subject>Wounds and Injuries - pathology</subject><subject>Wounds and Injuries - physiopathology</subject><issn>0077-8923</issn><issn>1749-6632</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkF1LwzAUhoMobk7_ghQvvGvNV5PGC0GH24RtMhwMr0LaptLZj5l0bPv3pnTMa3NzCHnPc3IeAO4QDJA7D-sAcSp8xggOMIQoaGJIBGbB_gz0T0_noA8h534kMOmBK2vXLoojyi9BDyEuQszCPgjnus6rJi9V4Y1qU6omrysvPnjD3CTbwl2rL--lrrQ3U8bUO2-oi8Jeg4tMFVbfHOsALEevy-HEn76P34bPUz-hMIp8yhClkIkME8EUERFhiopUcY0IgjriihIdi4xgCglRkGGssjSMwlgxlDIyAPcddmPqn622jSxzm7gPqErXWyu544aUtMHHLpiY2lqjM7kxbiVzkAjK1plcy1aMbMXI1pk8OpN713x7nLKNS53-tR4lucBTF9jlhT78Ay3nn88fKHIAvwPkttH7E0CZb8k44aFczcdywRaYTiYrOSO_8ceJPQ</recordid><startdate>200112</startdate><enddate>200112</enddate><creator>CAMPBELL, JULIE H.</creator><creator>HAN, CHIH-LU</creator><creator>CAMPBELL, GORDON R.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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>7X8</scope></search><sort><creationdate>200112</creationdate><title>Neointimal Formation by Circulating Bone Marrow Cells</title><author>CAMPBELL, JULIE H. ; HAN, CHIH-LU ; CAMPBELL, GORDON R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4088-46144069f2396a39836a49da7e1310e87a43eb9f324033a0622afd585ba61d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Arteriosclerosis - pathology</topic><topic>Arteriosclerosis - physiopathology</topic><topic>bone marrow cells</topic><topic>Bone Marrow Cells - cytology</topic><topic>Bone Marrow Cells - pathology</topic><topic>Cell Movement</topic><topic>Humans</topic><topic>smooth muscle cells</topic><topic>Tunica Intima - cytology</topic><topic>Tunica Intima - pathology</topic><topic>vascular healing</topic><topic>Wounds and Injuries - pathology</topic><topic>Wounds and Injuries - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CAMPBELL, JULIE H.</creatorcontrib><creatorcontrib>HAN, CHIH-LU</creatorcontrib><creatorcontrib>CAMPBELL, GORDON R.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Annals of the New York Academy of Sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CAMPBELL, JULIE H.</au><au>HAN, CHIH-LU</au><au>CAMPBELL, GORDON R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neointimal Formation by Circulating Bone Marrow Cells</atitle><jtitle>Annals of the New York Academy of Sciences</jtitle><addtitle>Ann N Y Acad Sci</addtitle><date>2001-12</date><risdate>2001</risdate><volume>947</volume><issue>1</issue><spage>18</spage><epage>25</epage><pages>18-25</pages><issn>0077-8923</issn><eissn>1749-6632</eissn><abstract>: The origin of smooth muscle cells involved in vascular healing was examined. Eighteen C57BL/6 (Ly 5.2) female mice underwent whole body irradiation followed by transfusion with 106 bone nucleated marrow cells from congenic (Ly 5.1) male donors. Successful repopulation by donor marrow was demonstrated after 4 weeks by flow cytometry with FITC‐conjugated A20.1/Ly 5.1 monoclonal antibody. The iliac artery of six of the chimeric mice was scratch‐injured by five passes of a probe, causing severe medial damage. After 4 weeks the arterial lumen was obliterated by a cell‐rich neointima, with α‐smooth muscle actin‐containing cells present around the residual lumen. Approximately half of these cells were of male donor origin, as evidenced by in situ hybridization with a Y chromosome‐specific probe. An organized arterial thrombus was formed in the remaining 12 chimeric mice by inserting an 8‐0 silk suture into the left common carotid artery. Donor cells staining with α‐smooth muscle actin were found in those arteries sustaining serious damage but not in arteries with minimal damage. Our results suggest that bone marrow‐derived cells are recruited in vascular healing as a complementary source of smooth muscle‐like cells when the media is severely damaged and few resident smooth muscle cells are available to effect repair.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>11795265</pmid><doi>10.1111/j.1749-6632.2001.tb03926.x</doi><tpages>8</tpages></addata></record> |
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subjects | Arteriosclerosis - pathology Arteriosclerosis - physiopathology bone marrow cells Bone Marrow Cells - cytology Bone Marrow Cells - pathology Cell Movement Humans smooth muscle cells Tunica Intima - cytology Tunica Intima - pathology vascular healing Wounds and Injuries - pathology Wounds and Injuries - physiopathology |
title | Neointimal Formation by Circulating Bone Marrow Cells |
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