Epigenetics and miRNA emerge as key regulators of smooth muscle cell phenotype and function

被引:21
作者
Clifford, Rachel L. [1 ,2 ]
Singer, Cherie A. [3 ]
John, Alison E. [1 ,2 ]
机构
[1] Univ Nottingham, Div Resp Med, Nottingham NG5 1PB, England
[2] City Hosp, Nottingham Resp Res Unit, Nottingham NG5 1PB, England
[3] Univ Nevada, Sch Med, Dept Pharmacol, Ctr Mol Med 573, Reno, NV 89557 USA
基金
美国国家卫生研究院; 英国惠康基金; 英国医学研究理事会;
关键词
Airway smooth muscle; Asthma; Epigenetics; Inflammation; microRNA; Remodeling; EXTRACELLULAR-SUPEROXIDE DISMUTASE; GLYCOGEN-SYNTHASE KINASE-3-BETA; ALLERGIC AIRWAY INFLAMMATION; DNA METHYLATION; PULMONARY-HYPERTENSION; HISTONE ACETYLATION; MICRORNA TARGETS; INTERFERON-GAMMA; MATRIX PROTEINS; BINDING PROTEIN;
D O I
10.1016/j.pupt.2012.07.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Regulation of phenotypic plasticity in smooth muscle requires an understanding of the mechanisms regulating phenotype-specific genes and the processes dysregulated during pathogenesis. Decades of study in airway smooth muscle has provided extensive knowledge of the gene expression patterns and signaling pathways necessary to maintain and alter smooth muscle cell phenotype. With this solid foundation, the importance and complexity of inheritable epigenetic modifications and mechanisms silencing gene expression have now emerged as fundamental components regulating aspects of inflammation, proliferation and remodeling. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:75 / 85
页数:11
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