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Histone deacetylases and cardiovascular cell lineage commitment 被引量:2

Histone deacetylases and cardiovascular cell lineage commitment
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摘要 Cardiovascular diseases(CVDs), which include alldiseases of the heart and circulation system, are the leading cause of deaths on the globally. During the development of CVDs, choric inflammatory, lipid metabolism disorder and endothelial dysfunction are widely recognized risk factors. Recently, the new treatment for CVDs that designed to regenerate the damaged myocardium and injured vascular endothelium and improve recovery by the use of stem cells, attracts more and more public attention. Histone deacetylases(HDACs) are a family of enzymes that remove acetyl groups from lysine residues of histone proteins allowing the histones to wrap the DNA more tightly and commonly known as epigenetic regulators of gene transcription. HDACs play indispensable roles in nearly all biological processes, such as transcriptional regulation, cell cycle progression and developmental events, and have originally shown to be involved in cancer and neurological diseases. HDACs are also found to play crucial roles in cardiovascular diseases by modulating vascular cell homeostasis(e.g., proliferation, migration, and apoptosis of both ECs and SMCs). This review focuses on the roles of different members of HDACs and HDAC inhibitor on stem cell/ progenitor cell differentiation toward vascular cell lineages(endothelial cells, smooth muscle cells and Cardiomyocytes) and its potential therapeutics. Cardiovascular diseases (CVDs), which include alldiseases of the heart and circulation system, arethe leading cause of deaths on the globally. Duringthe development of CVDs, choric inflammatory, lipidmetabolism disorder and endothelial dysfunction arewidely recognized risk factors. Recently, the newtreatment for CVDs that designed to regenerate thedamaged myocardium and injured vascular endotheliumand improve recovery by the use of stem cells, attractsmore and more public attention. Histone deacetylases(HDACs) are a family of enzymes that remove acetylgroups from lysine residues of histone proteinsallowing the histones to wrap the DNA more tightlyand commonly known as epigenetic regulators ofgene transcription. HDACs play indispensable roles innearly all biological processes, such as transcriptionalregulation, cell cycle progression and developmentalevents, and have originally shown to be involved incancer and neurological diseases. HDACs are alsofound to play crucial roles in cardiovascular diseases bymodulating vascular cell homeostasis (e.g. , proliferation,migration, and apoptosis of both ECs and SMCs). Thisreview focuses on the roles of different members ofHDACs and HDAC inhibitor on stem cell/ progenitor celldifferentiation toward vascular cell lineages (endothelialcells, smooth muscle cells and Cardiomyocytes) and itspotential therapeutics.
出处 《World Journal of Stem Cells》 SCIE CAS 2015年第5期852-859,共8页 世界干细胞杂志(英文版)(电子版)
基金 Supported by British Heart Foundation project,No.PG13-63-30419
关键词 HISTONE DEACETYLASES Stem CELL ENDOTHELIALCELL Smooth muscle CELL CARDIOVASCULAR diseases Histone deacetylases Stem cell Endothelial cell Smooth muscle cell Cardiovascular diseases
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  • 1Sun L, Ma C, Liu S, Zou L, Jia D. Mitral annular tissue velocity inthe diagnosis of coronary artery disease. Eur Rev Med PharmacolSci 2014; 18: 3754-3760 [PMID: 25555863].
  • 2Kinlay S, Libby P, Ganz P. Endothelial function and coronary arterydisease. Curr Opin Lipidol 2001; 12: 383-389 [PMID: 11507322].
  • 3Davignon J, Ganz P. Role of endothelial dysfunction inatherosclerosis. Circulation 2004; 109: III27-III32 [PMID: 15198963DOI: 10.1161/01.CIR.0000131515.03336.f8].
  • 4Anderson TJ. Nitric oxide, atherosclerosis and the clinical relevanceof endothelial dysfunction. Heart Fail Rev 2003; 8: 71-86 [PMID:12652161].
  • 5Malgieri A, Kantzari E, Patrizi MP, Gambardella S. Bone marrowand umbilical cord blood human mesenchymal stem cells: state ofthe art. Int J Clin Exp Med 2010; 3: 248-269 [PMID: 21072260].
  • 6Beltrami AP, Barlucchi L, Torella D, Baker M, Limana F, ChimentiS, Kasahara H, Rota M, Musso E, Urbanek K, Leri A, Kajstura J,Nadal-Ginard B, Anversa P. Adult cardiac stem cells are multipotentand support myocardial regeneration. Cell 2003; 114: 763-776[PMID: 14505575].
  • 7Findeisen HM, Gizard F, Zhao Y, Qing H, Heywood EB, JonesKL, Cohn D, Bruemmer D. Epigenetic regulation of vascularsmooth muscle cell proliferation and neointima formation by histonedeacetylase inhibition. Arterioscler Thromb Vasc Biol 2011; 31:851-860 [PMID: 21233448 DOI: 10.1161/ATVBAHA.110.221952].
  • 8Berndsen CE, Denu JM. Catalysis and substrate selection byhistone/protein lysine acetyltransferases. Curr Opin Struct Biol 2008;18: 682-689 [PMID: 19056256 DOI: 10.1016/j.sbi.2008.11.004].
  • 9Lee JH, Hart SR, Skalnik DG. Histone deacetylase activity isrequired for embryonic stem cell differentiation. Genesis 2004; 38:32-38 [PMID: 14755802 DOI: 10.1002/gene.10250].
  • 10Thiagalingam S, Cheng KH, Lee HJ, Mineva N, ThiagalingamA, Ponte JF. Histone deacetylases: unique players in shaping theepigenetic histone code. Ann N Y Acad Sci 2003; 983: 84-100 [PMID:12724214].

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