Intimal proliferation in an organ culture of human internal mammary artery

Objective: Intimal smooth muscle cell proliferation is an early feature of atherosclerosis. Its progression is difficult to monitor in humans and previous studies have mostly relied on necropsy material. The aim of this study was therefore to establish whether intimal proliferation occurred in an or...

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Veröffentlicht in:Cardiovascular research 1992-12, Vol.26 (12), p.1189-1194
Hauptverfasser: Holt, Cathy M, Francis, Sheila E, Rogers, Suzanne, Gadsdon, Patricia A, Taylor, Trevor, Clelland, Colin, Soyombo, Abigail, Newby, Andrew C, Angelini, Gianni D
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container_end_page 1194
container_issue 12
container_start_page 1189
container_title Cardiovascular research
container_volume 26
creator Holt, Cathy M
Francis, Sheila E
Rogers, Suzanne
Gadsdon, Patricia A
Taylor, Trevor
Clelland, Colin
Soyombo, Abigail
Newby, Andrew C
Angelini, Gianni D
description Objective: Intimal smooth muscle cell proliferation is an early feature of atherosclerosis. Its progression is difficult to monitor in humans and previous studies have mostly relied on necropsy material. The aim of this study was therefore to establish whether intimal proliferation occurred in an organ culture of human internal mammary artery. Methods: Segments of freshly isolated internal mammary artery were maintained in standard tissue culture medium containing 30% calf serum for 14 d. Tissue viability (measured by ATP concentration) was maintained during processing and throughout the culture period [211(SEM 28) nmol ATP·g−1 wet weight on d 1 v 208(27) on d 14]. Results: Histological transverse sections of cultured internal mammary artery showed the development of α neointima containing smooth muscle cells identified by immunocytochemistry for a actin. Pulse labelling of cultures with [3H]-thymidine showed proliferating cells predominantly in a neointimal layer with few dividing cells in the media. Cultured de-endothelialised vessels showed less neointimal thickening than cultured freshly isolated vessels [16(3) v 36(5) μm, p
doi_str_mv 10.1093/cvr/26.12.1189
format Article
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Its progression is difficult to monitor in humans and previous studies have mostly relied on necropsy material. The aim of this study was therefore to establish whether intimal proliferation occurred in an organ culture of human internal mammary artery. Methods: Segments of freshly isolated internal mammary artery were maintained in standard tissue culture medium containing 30% calf serum for 14 d. Tissue viability (measured by ATP concentration) was maintained during processing and throughout the culture period [211(SEM 28) nmol ATP·g−1 wet weight on d 1 v 208(27) on d 14]. Results: Histological transverse sections of cultured internal mammary artery showed the development of α neointima containing smooth muscle cells identified by immunocytochemistry for a actin. Pulse labelling of cultures with [3H]-thymidine showed proliferating cells predominantly in a neointimal layer with few dividing cells in the media. Cultured de-endothelialised vessels showed less neointimal thickening than cultured freshly isolated vessels [16(3) v 36(5) μm, p&lt;0.0025] as well as a reduced number of dividing cells per mm of neointimal length [3.1(0.6) v 5.5(1.1), p&lt;0.05]. Conclusions: Intimal proliferation occurred in organ culture of internal mammary artery. There is evidence for a factor derived from the endothelium, which may be important in the development of intimal proliferation. Cardiovascular Research 1992;26:1189-1194</description><identifier>ISSN: 0008-6363</identifier><identifier>EISSN: 1755-3245</identifier><identifier>DOI: 10.1093/cvr/26.12.1189</identifier><identifier>PMID: 1288865</identifier><identifier>CODEN: CVREAU</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Aged ; Arteriosclerosis - pathology ; Atherosclerosis (general aspects, experimental research) ; Biological and medical sciences ; Blood and lymphatic vessels ; Cardiology. 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Its progression is difficult to monitor in humans and previous studies have mostly relied on necropsy material. The aim of this study was therefore to establish whether intimal proliferation occurred in an organ culture of human internal mammary artery. Methods: Segments of freshly isolated internal mammary artery were maintained in standard tissue culture medium containing 30% calf serum for 14 d. Tissue viability (measured by ATP concentration) was maintained during processing and throughout the culture period [211(SEM 28) nmol ATP·g−1 wet weight on d 1 v 208(27) on d 14]. Results: Histological transverse sections of cultured internal mammary artery showed the development of α neointima containing smooth muscle cells identified by immunocytochemistry for a actin. Pulse labelling of cultures with [3H]-thymidine showed proliferating cells predominantly in a neointimal layer with few dividing cells in the media. Cultured de-endothelialised vessels showed less neointimal thickening than cultured freshly isolated vessels [16(3) v 36(5) μm, p&lt;0.0025] as well as a reduced number of dividing cells per mm of neointimal length [3.1(0.6) v 5.5(1.1), p&lt;0.05]. Conclusions: Intimal proliferation occurred in organ culture of internal mammary artery. There is evidence for a factor derived from the endothelium, which may be important in the development of intimal proliferation. Cardiovascular Research 1992;26:1189-1194</description><subject>Aged</subject><subject>Arteriosclerosis - pathology</subject><subject>Atherosclerosis (general aspects, experimental research)</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Cardiology. 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Vascular system</topic><topic>Cell Division - physiology</topic><topic>Culture Techniques</topic><topic>Endothelium - cytology</topic><topic>Endothelium - ultrastructure</topic><topic>Female</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>internal mammary artery</topic><topic>intimal proliferation</topic><topic>Male</topic><topic>Mammary Arteries - cytology</topic><topic>Mammary Arteries - ultrastructure</topic><topic>Medical sciences</topic><topic>Microscopy, Electron</topic><topic>Middle Aged</topic><topic>Muscle, Smooth - cytology</topic><topic>organ culture</topic><topic>Tunica Intima - cytology</topic><topic>Tunica Intima - ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Holt, Cathy M</creatorcontrib><creatorcontrib>Francis, Sheila E</creatorcontrib><creatorcontrib>Rogers, Suzanne</creatorcontrib><creatorcontrib>Gadsdon, Patricia A</creatorcontrib><creatorcontrib>Taylor, Trevor</creatorcontrib><creatorcontrib>Clelland, Colin</creatorcontrib><creatorcontrib>Soyombo, Abigail</creatorcontrib><creatorcontrib>Newby, Andrew C</creatorcontrib><creatorcontrib>Angelini, Gianni D</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</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>Cardiovascular research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Holt, Cathy M</au><au>Francis, Sheila E</au><au>Rogers, Suzanne</au><au>Gadsdon, Patricia A</au><au>Taylor, Trevor</au><au>Clelland, Colin</au><au>Soyombo, Abigail</au><au>Newby, Andrew C</au><au>Angelini, Gianni D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Intimal proliferation in an organ culture of human internal mammary artery</atitle><jtitle>Cardiovascular research</jtitle><addtitle>Cardiovasc Res</addtitle><date>1992-12-01</date><risdate>1992</risdate><volume>26</volume><issue>12</issue><spage>1189</spage><epage>1194</epage><pages>1189-1194</pages><issn>0008-6363</issn><eissn>1755-3245</eissn><coden>CVREAU</coden><abstract>Objective: Intimal smooth muscle cell proliferation is an early feature of atherosclerosis. Its progression is difficult to monitor in humans and previous studies have mostly relied on necropsy material. The aim of this study was therefore to establish whether intimal proliferation occurred in an organ culture of human internal mammary artery. Methods: Segments of freshly isolated internal mammary artery were maintained in standard tissue culture medium containing 30% calf serum for 14 d. Tissue viability (measured by ATP concentration) was maintained during processing and throughout the culture period [211(SEM 28) nmol ATP·g−1 wet weight on d 1 v 208(27) on d 14]. Results: Histological transverse sections of cultured internal mammary artery showed the development of α neointima containing smooth muscle cells identified by immunocytochemistry for a actin. Pulse labelling of cultures with [3H]-thymidine showed proliferating cells predominantly in a neointimal layer with few dividing cells in the media. Cultured de-endothelialised vessels showed less neointimal thickening than cultured freshly isolated vessels [16(3) v 36(5) μm, p&lt;0.0025] as well as a reduced number of dividing cells per mm of neointimal length [3.1(0.6) v 5.5(1.1), p&lt;0.05]. Conclusions: Intimal proliferation occurred in organ culture of internal mammary artery. There is evidence for a factor derived from the endothelium, which may be important in the development of intimal proliferation. Cardiovascular Research 1992;26:1189-1194</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>1288865</pmid><doi>10.1093/cvr/26.12.1189</doi><tpages>6</tpages></addata></record>
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source MEDLINE; Oxford University Press Journals Digital Archive Legacy
subjects Aged
Arteriosclerosis - pathology
Atherosclerosis (general aspects, experimental research)
Biological and medical sciences
Blood and lymphatic vessels
Cardiology. Vascular system
Cell Division - physiology
Culture Techniques
Endothelium - cytology
Endothelium - ultrastructure
Female
Humans
Immunohistochemistry
internal mammary artery
intimal proliferation
Male
Mammary Arteries - cytology
Mammary Arteries - ultrastructure
Medical sciences
Microscopy, Electron
Middle Aged
Muscle, Smooth - cytology
organ culture
Tunica Intima - cytology
Tunica Intima - ultrastructure
title Intimal proliferation in an organ culture of human internal mammary artery
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