The mechanism of stem cell differentiation into smooth muscle cells

被引:28
作者
Xiao, Qingzhong [1 ]
Wang, Gang [1 ]
Luo, Zhenling [1 ]
Xu, Qingbo [1 ]
机构
[1] Kings Coll London, BHF Ctr, Div Cardiovasc, London SE5 9NU, England
关键词
Stem cells; smooth muscle cells; differentiation; vascular disease; 3-DIMENSIONAL CULTURE-SYSTEMS; II HISTONE DEACETYLASES; MARKER GENE-EXPRESSION; NAD(P)H OXIDASES; PROGENITOR CELLS; MICRORNA REGULATION; ANGIOTENSIN-II; COLLAGEN-IV; IN-VIVO; MATRIX;
D O I
10.1160/TH09-11-0794
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Stem cells represent one of the most promising areas in biological and medical research. All stem cells are defined as having two basic properties: unlimited self-renewal and the broad potential to differentiate in vitro, via "progenitor cells", into somatic cells of many tissue types, in which smooth muscle cell (SMC) differentiation is a complicated and not well defined process. It is known that serum response factors (SRF) and co-activator myocardin are essential transcription factors in SMC differentiation. Upstream activators or regulators for the transcription factors have been recently identified, such as reactive oxygen species, histone deacetylases, microRNAs and extracellular matrix (ECM) proteins and integrins. In this review we, therefore, aim to briefly summarise recent progress in the mechanism of stem cell differentiation into SMCs to highlight the potential targets for promoting/inhibiting SMC differentiation useful for vessel-tissue engineering and treatment of vascular disease.
引用
收藏
页码:440 / 448
页数:9
相关论文
共 86 条
[1]   Stem cell therapy for vascular disease [J].
Adams, Benjamin ;
Xiao, Qingzhong ;
Xu, Qingbo .
TRENDS IN CARDIOVASCULAR MEDICINE, 2007, 17 (07) :246-251
[2]   Vascular progenitor cells and atherosclerosis [J].
Adams, Benjamin ;
Xiao, Qingzhong ;
Xu, Qingbo .
FUTURE CARDIOLOGY, 2007, 3 (06) :635-645
[3]   Collagens in the progression and complications of atherosclerosis [J].
Adiguzel, Eser ;
Ahmad, Pamela J. ;
Franco, Christopher ;
Bendeck, Michelle P. .
VASCULAR MEDICINE, 2009, 14 (01) :73-89
[4]   Control of cardiac growth by histone acetylation/deacetylation [J].
Backs, J ;
Olson, EN .
CIRCULATION RESEARCH, 2006, 98 (01) :15-24
[5]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[6]   Acquisition of the contractile phenotype by murine arterial smooth muscle cells depends on the Mir143/145 gene cluster [J].
Boettger, Thomas ;
Beetz, Nadine ;
Kostin, Sawa ;
Schneider, Johanna ;
Krueger, Marcus ;
Hein, Lutz ;
Braun, Thomas .
JOURNAL OF CLINICAL INVESTIGATION, 2009, 119 (09) :2634-2647
[7]   MicroRNA-92a Controls Angiogenesis and Functional Recovery of Ischemic Tissues in Mice [J].
Bonauer, Angelika ;
Carmona, Guillaume ;
Iwasaki, Masayoshi ;
Mione, Marina ;
Koyanagi, Masamichi ;
Fischer, Ariane ;
Burchfield, Jana ;
Fox, Henrik ;
Doebele, Carmen ;
Ohtani, Kisho ;
Chavakis, Emmanouil ;
Potente, Michael ;
Tjwa, Marc ;
Urbich, Carmen ;
Zeiher, Andreas M. ;
Dimmeler, Stefanie .
SCIENCE, 2009, 324 (5935) :1710-1713
[8]   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
[9]   Multilineage differentiation of rhesus monkey embryonic stem cells in three-dimensional culture systems [J].
Chen, SS ;
Revoltella, RP ;
Papini, S ;
Michelini, M ;
Fitzgerald, W ;
Zimmerberg, J ;
Margolis, L .
STEM CELLS, 2003, 21 (03) :281-295
[10]   Granzyme B induces smooth muscle cell apoptosis in the absence of perforin - Involvement of extracellular matrix degradation [J].
Choy, JC ;
Hung, VHY ;
Hunter, AL ;
Cheung, PK ;
Motyka, B ;
Goping, IS ;
Sawchuk, T ;
Bleackley, RC ;
Podor, TJ ;
McManus, BM ;
Granville, DJ .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (12) :2245-2250