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Infiltration/accumulation of low density lipoproteins in endothelial/smooth muscle cell co-culture preparations with different modes

  • Beihang University

科研成果: 书/报告/会议事项章节会议稿件同行评审

摘要

Using different endothelial/smooth muscle cell co-culture modes to simulate the intimal structure of blood vessels, the water filtration rate and the infiltration/accumulation of LDL of the cultured cell layers were studied. The three cell culture modes of the study were: i) endothelial cell monolayer (EC/Φ); ii) endothelial cells directly co-cultured on the smooth muscle cell monolayer (EC-SMC); iii) endothelial cells and smooth muscle cells cultured on different sides of a Millicell- CM membrane (EC/SMC). It was found that under the same condition, the water filtration rate was the lowest for EC/SMC mode and the highest for EC/Φ mode, while the infiltration/ accumulation of DiI-LDLs was the lowest in the EC/Φ mode and the highest in the EC-SMC mode. It was also found that the values of DiI-LDL infiltration/accumulation in the cultured cell layers increased with increasing the water filtration rate, vw. The results from the in vitro model study therefore suggest that the infiltration/ accumulation of the lipids within the arterial wall is positively correlated with concentration polarization of atherogenic lipids, and the integrity of the endothelium plays an important role in the penetration and accumulation of atherogenic lipids in blood vessel walls.

源语言英语
主期刊名World Congress on Medical Physics and Biomedical Engineering
主期刊副标题Biomaterials, Cellular and Tissue Engineering, Artificial Organs
出版商Springer Verlag
30-33
页数4
版本10
ISBN(印刷版)9783642038990
DOI
出版状态已出版 - 2009
活动World Congress on Medical Physics and Biomedical Engineering: Biomaterials, Cellular and Tissue Engineering, Artificial Organs - Munich, 德国
期限: 7 9月 200912 9月 2009

丛书

姓名IFMBE Proceedings
编号10
25
ISSN(印刷版)1680-0737

会议

会议World Congress on Medical Physics and Biomedical Engineering: Biomaterials, Cellular and Tissue Engineering, Artificial Organs
国家/地区德国
Munich
时期7/09/0912/09/09

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