A cell culture model using rat coronary artery adventitial fibroblasts to measure collagen production

<p>Abstract</p> <p>Background</p> <p>We have developed a rat cell model for studying collagen type I production in coronary artery adventitial fibroblasts. Increased deposition of adventitial collagen type I leads to stiffening of the blood vessel, increased blood press...

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Main Authors: Meszaros Gary, Doane Kathleen, Milsted Amy, Jenkins Cathleen, Toot Jonathan, Ely Daniel
Format: Article
Language:English
Published: BMC 2007-05-01
Series:BMC Cardiovascular Disorders
Online Access:http://www.biomedcentral.com/1471-2261/7/13
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spelling doaj-55a417a2ac514607a8fa76ce8db687362020-11-25T03:48:51ZengBMCBMC Cardiovascular Disorders1471-22612007-05-01711310.1186/1471-2261-7-13A cell culture model using rat coronary artery adventitial fibroblasts to measure collagen productionMeszaros GaryDoane KathleenMilsted AmyJenkins CathleenToot JonathanEly Daniel<p>Abstract</p> <p>Background</p> <p>We have developed a rat cell model for studying collagen type I production in coronary artery adventitial fibroblasts. Increased deposition of adventitial collagen type I leads to stiffening of the blood vessel, increased blood pressure, arteriosclerosis and coronary heart disease. Although the source and mechanism of collagen deposition is yet unknown, the adventitia appears to play a significant role. To demonstrate the application of our cell model, cultured adventitial fibroblasts were treated with sex hormones and the effect on collagen production measured.</p> <p>Methods</p> <p>Hearts (10–12 weeks) were harvested and the left anterior descending coronary artery (LAD) was isolated and removed. Tissue explants were cultured and cells (passages 2–4) were confirmed as fibroblasts using immunohistochemistry. Optimal conditions were determined for cell tissue harvest, timing, proliferation and culture conditions. Fibroblasts were exposed to 10<sup>-7 </sup>M testosterone or 10<sup>-7 </sup>M estrogen for 24 hours and either immunostained for collagen type I or subjected to ELISA.</p> <p>Results</p> <p>Results showed increased collagen staining in fibroblasts treated with testosterone compared to control and decreased staining with estrogen. ELISA results showed that testosterone increased collagen I by 20% whereas estrogen decreased collagen I by 15%.</p> <p>Conclusion</p> <p>Data demonstrates the usefulness of our cell model in studying the specific role of the adventitia apart from other blood vessel tissue in rat coronary arteries. Results suggest opposite effects of testosterone and estrogen on collagen synthesis in the rat coronary artery adventitial fibroblasts.</p> http://www.biomedcentral.com/1471-2261/7/13
collection DOAJ
language English
format Article
sources DOAJ
author Meszaros Gary
Doane Kathleen
Milsted Amy
Jenkins Cathleen
Toot Jonathan
Ely Daniel
spellingShingle Meszaros Gary
Doane Kathleen
Milsted Amy
Jenkins Cathleen
Toot Jonathan
Ely Daniel
A cell culture model using rat coronary artery adventitial fibroblasts to measure collagen production
BMC Cardiovascular Disorders
author_facet Meszaros Gary
Doane Kathleen
Milsted Amy
Jenkins Cathleen
Toot Jonathan
Ely Daniel
author_sort Meszaros Gary
title A cell culture model using rat coronary artery adventitial fibroblasts to measure collagen production
title_short A cell culture model using rat coronary artery adventitial fibroblasts to measure collagen production
title_full A cell culture model using rat coronary artery adventitial fibroblasts to measure collagen production
title_fullStr A cell culture model using rat coronary artery adventitial fibroblasts to measure collagen production
title_full_unstemmed A cell culture model using rat coronary artery adventitial fibroblasts to measure collagen production
title_sort cell culture model using rat coronary artery adventitial fibroblasts to measure collagen production
publisher BMC
series BMC Cardiovascular Disorders
issn 1471-2261
publishDate 2007-05-01
description <p>Abstract</p> <p>Background</p> <p>We have developed a rat cell model for studying collagen type I production in coronary artery adventitial fibroblasts. Increased deposition of adventitial collagen type I leads to stiffening of the blood vessel, increased blood pressure, arteriosclerosis and coronary heart disease. Although the source and mechanism of collagen deposition is yet unknown, the adventitia appears to play a significant role. To demonstrate the application of our cell model, cultured adventitial fibroblasts were treated with sex hormones and the effect on collagen production measured.</p> <p>Methods</p> <p>Hearts (10–12 weeks) were harvested and the left anterior descending coronary artery (LAD) was isolated and removed. Tissue explants were cultured and cells (passages 2–4) were confirmed as fibroblasts using immunohistochemistry. Optimal conditions were determined for cell tissue harvest, timing, proliferation and culture conditions. Fibroblasts were exposed to 10<sup>-7 </sup>M testosterone or 10<sup>-7 </sup>M estrogen for 24 hours and either immunostained for collagen type I or subjected to ELISA.</p> <p>Results</p> <p>Results showed increased collagen staining in fibroblasts treated with testosterone compared to control and decreased staining with estrogen. ELISA results showed that testosterone increased collagen I by 20% whereas estrogen decreased collagen I by 15%.</p> <p>Conclusion</p> <p>Data demonstrates the usefulness of our cell model in studying the specific role of the adventitia apart from other blood vessel tissue in rat coronary arteries. Results suggest opposite effects of testosterone and estrogen on collagen synthesis in the rat coronary artery adventitial fibroblasts.</p>
url http://www.biomedcentral.com/1471-2261/7/13
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