New Aspects of Vascular Calcification: Histone Deacetylases and Beyond

被引:21
作者
Kwon, Duk-Hwa [1 ,2 ]
Kim, Young-Kook [2 ,3 ,4 ]
Kook, Hyun [1 ,2 ]
机构
[1] Chonnam Natl Univ, Med Sch, Dept Pharmacol, 42 Jebong Ro, Gwangju 61469, South Korea
[2] Chonnam Natl Univ, Med Sch, Basic Res Lab Cardiac Remodeling, Gwangju, South Korea
[3] Chonnam Natl Univ, Ctr Creat Biomed Scientists, Gwangju, South Korea
[4] Chonnam Natl Univ, Med Sch, Dept Biochem, Gwangju, South Korea
基金
新加坡国家研究基金会;
关键词
Vascular Calcification; Histone Deacetylase; MDM2; Posttranslational Modification; SMOOTH-MUSCLE-CELLS; BONE MORPHOGENETIC PROTEIN-2; ENDOPLASMIC-RETICULUM STRESS; RECEPTOR-DEFICIENT MICE; MATRIX GLA PROTEIN; CARDIAC-HYPERTROPHY; CARDIOVASCULAR CALCIFICATION; ARTERIAL CALCIFICATION; UP-REGULATION; CLASS-I;
D O I
10.3346/jkms.2017.32.11.1738
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Vascular calcification is a pathologic phenomenon in which calcium phosphate is ectopically deposited in the arteries. Previously, calcification was considered to be a passive process in response to metabolic diseases, vascular or valvular diseases, or even aging. However, now calcification is recognized as a highly-regulated consequence, like bone formation, and many clinical trials have been carried out to elucidate the correlation between vascular calcification and cardiovascular events and mortality. As a result, vascular calcification has been implicated as an independent risk factor in cardiovascular diseases. Many molecules are now known to be actively associated with this process. Recently, our laboratory found that posttranslational modification of histone deacetylase (HDAC) 1 is actively involved in the development of vascular calcification. In addition, we found that modulation of the activity of HDAC as well as its protein stability by MDM2, an HDAC1-E3 ligase, may be a therapeutic target in vascular calcification. In the present review, we overview the pathomechanism of vascular calcification and the involvement of posttranslational modification of epigenetic regulators.
引用
收藏
页码:1738 / 1748
页数:11
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