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Cholesterol Loading Reprograms the MicroRNA-143/145–Myocardin Axis to Convert Aortic Smooth Muscle Cells to a Dysfunctional Macrophage-Like Phenotype
Author(s) -
Yuliya Vengrenyuk,
Hitoo Nishi,
Xiaochun Long,
Mireille Ouimet,
Nazir Savji,
Fernando O. Martínez,
Courtney P. Cassella,
Kathryn J. Moore,
Stephen A. Ramsey,
Joseph M. Miano,
Edward A. Fisher
Publication year - 2015
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.114.304029
Subject(s) - myocardin , microrna , phenotype , smooth muscle , dysfunctional family , biology , macrophage , microbiology and biotechnology , anatomy , pathology , endocrinology , medicine , genetics , gene , gene expression , serum response factor , in vitro , clinical psychology
We previously showed that cholesterol loading in vitro converts mouse aortic vascular smooth muscle cells (VSMC) from a contractile state to one resembling macrophages. In human and mouse atherosclerotic plaques, it has become appreciated that ≈40% of cells classified as macrophages by histological markers may be of VSMC origin. Therefore, we sought to gain insight into the molecular regulation of this clinically relevant process.

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