Fate and State of Vascular Smooth Muscle Cells in Atherosclerosis

被引:227
作者
Miano, Joseph M. [1 ,2 ]
Fisher, Edward A. [3 ]
Majesky, Mark W. [4 ]
机构
[1] Augusta Univ, Med Coll Georgia, Dept Med, Augusta, GA USA
[2] Augusta Univ, Med Coll Georgia, Vasc Biol Ctr, CL-3060,1460 Laney Walker Blvd, Augusta, GA 30912 USA
[3] NYU, Sch Med, Dept Med, Cardiovasc Res Ctr,Div Cardiol, New York, NY USA
[4] Univ Washington, Dept Pediat, Ctr Dev Biol & Regenerat Med, Seattle Childrens Res Inst, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
atherosclerosis; cell differentiation; myocytes; smooth muscle; genetics; genomics; MACROPHAGE-LIKE CELLS; MYOCARDIN; GENE; TRANSDIFFERENTIATION; IDENTIFICATION; CONTRIBUTES;
D O I
10.1161/CIRCULATIONAHA.120.049922
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Vascular smooth muscle cells (VSMCs) have long been associated with phenotypic modulation/plasticity or dedifferentiation. Innovative technologies in cell lineage tracing, single-cell RNA sequencing, and human genomics have been integrated to gain unprecedented insights into the molecular reprogramming of VSMCs to other cell phenotypes in experimental and clinical atherosclerosis. The current thinking is that an apparently small subset of contractile VSMCs undergoes a fate switch to transitional, multipotential cells that can adopt plaque-destabilizing (inflammation, ossification) or plaque-stabilizing (collagen matrix deposition) cell states. Several candidate mediators of such VSMC fate and state changes are coming to light with intriguing implications for understanding coronary artery disease risk and the development of new treatment modalities. Here, we briefly summarize some technical and conceptual advancements derived from 2 publications in Circulation and another in Nature Medicine that, collectively, illuminate new research directions to further explore the role of VSMCs in atherosclerotic disease.
引用
收藏
页码:2110 / 2116
页数:7
相关论文
共 44 条
[1]   Stem Cell Pluripotency Genes Klf4 and Oct4 Regulate Complex SMC Phenotypic Changes Critical in Late-Stage Atherosclerotic Lesion Pathogenesis [J].
Alencar, Gabriel F. ;
Owsiany, Katherine M. ;
Karnewar, Santosh ;
Sukhavasi, Katyayani ;
Mocci, Giuseppe ;
Nguyen, Anh T. ;
Williams, Corey M. ;
Shamsuzzaman, Sohel ;
Mokry, Michal ;
Henderson, Christopher A. ;
Haskins, Ryan ;
Baylis, Richard A. ;
Finn, Aloke V. ;
McNamara, Coleen A. ;
Zunder, Eli R. ;
Venkata, Vamsidhar ;
Pasterkamp, Gerard ;
Bjorkegren, Johan ;
Bekiranov, Stefan ;
Owens, Gary K. .
CIRCULATION, 2020, 142 (21) :2045-2059
[2]   Contribution of Intimal Smooth Muscle Cells to Cholesterol Accumulation and Macrophage-Like Cells in Human Atherosclerosis [J].
Allahverdian, Sima ;
Chehroudi, Ali Cyrus ;
McManus, Bruce M. ;
Abraham, Thomas ;
Francis, Gordon A. .
CIRCULATION, 2014, 129 (15) :1551-1559
[3]   Search-and-replace genome editing without double-strand breaks or donor DNA [J].
Anzalone, Andrew V. ;
Randolph, Peyton B. ;
Davis, Jessie R. ;
Sousa, Alexander A. ;
Koblan, Luke W. ;
Levy, Jonathan M. ;
Chen, Peter J. ;
Wilson, Christopher ;
Newby, Gregory A. ;
Raguram, Aditya ;
Liu, David R. .
NATURE, 2019, 576 (7785) :149-+
[4]   IDENTIFICATION OF MACROPHAGES AND SMOOTH-MUSCLE CELLS IN HUMAN ATHEROSCLEROSIS USING MONOCLONAL-ANTIBODIES [J].
AQEL, NM ;
BALL, RY ;
WALDMANN, H ;
MITCHINSON, MJ .
JOURNAL OF PATHOLOGY, 1985, 146 (03) :197-204
[5]   EVIDENCE FOR A MONOCLONAL ORIGIN OF HUMAN ATHEROSCLEROTIC PLAQUES [J].
BENDITT, EP ;
BENDITT, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1973, 70 (06) :1753-1756
[6]   Vascular Smooth Muscle Cells in Atherosclerosis [J].
Bennett, Martin R. ;
Sinha, Sanjay ;
Owens, Gary K. .
CIRCULATION RESEARCH, 2016, 118 (04) :692-702
[7]   The Fat-Fed Apolipoprotein E Knockout Mouse Brachiocephalic Artery in the Study of Atherosclerotic Plaque Rupture [J].
Bond, Andrew R. ;
Jackson, Christopher L. .
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2011,
[8]   Extensive Proliferation of a Subset of Differentiated, yet Plastic, Medial Vascular Smooth Muscle Cells Contributes to Neointimal Formation in Mouse Injury and Atherosclerosis Models [J].
Chappell, Joel ;
Harman, Jennifer L. ;
Narasimhan, Vagheesh M. ;
Yu, Haixiang ;
Foote, Kirsty ;
Simons, Benjamin D. ;
Bennett, Martin R. ;
Jorgensen, Helle F. .
CIRCULATION RESEARCH, 2016, 119 (12) :1313-1323
[9]   Cholesterol-Induced Phenotypic Modulation of Smooth Muscle Cells to Macrophage/Fibroblast-like Cells Is Driven by an Unfolded Protein Response [J].
Chattopadhyay, Abhijnan ;
Kwartler, Callie S. ;
Kaw, Kaveeta ;
Li, Yanming ;
Kaw, Anita ;
Chen, Jiyuan ;
LeMaire, Scott A. ;
Shen, Ying H. ;
Milewicz, Dianna M. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2021, 41 (01) :302-316
[10]   Myocardin: A component of a molecular switch for smooth muscle differentiation [J].
Chen, JY ;
Kitchen, CM ;
Streb, JW ;
Miano, JM .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2002, 34 (10) :1345-1356