HDAC3 and HDAC7 Have Opposite Effects on Osteoclast Differentiation

被引:74
|
作者
Lan Pham [2 ]
Kaiser, Bria [2 ]
Romsa, Amanda [2 ]
Schwarz, Toni [2 ]
Gopalakrishnan, Raj [1 ]
Jensen, Eric D. [1 ]
Mansky, Kim C. [2 ]
机构
[1] Univ Minnesota, Sch Dent, Dept Diagnost & Biol Sci, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Dent, Dept Dev & Surg Sci, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
MICROPHTHALMIA TRANSCRIPTION FACTOR; HISTONE DEACETYLASE INHIBITORS; OSTEOBLAST DIFFERENTIATION; TRICHOSTATIN-A; FACTOR FAMILY; P38; MAPK; C-FOS; MITF; RUNX2; TARGET;
D O I
10.1074/jbc.M110.216853
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Histone deacetylases (HDACs) are negative regulators of transcription. Endochondral bone formation including chondrocyte and osteoblast maturation is regulated by HDACs. Very little is known about the role HDACs play in osteoclast differentiation. It has been previously reported that HDAC inhibitors, trichostatin A and sodium butyrate, suppress osteoclast differentiation through multiple mechanisms. In this study, we report that suppression of HDAC3 expression similar to HDAC inhibitors inhibits osteoclast differentiation, whereas osteoclasts suppressed for HDAC7 expression had accelerated differentiation when compared with control cells. Mitf, a transcription factor, is necessary for osteoclast differentiation. We demonstrate that Mitf and HDAC7 interact in RAW 264 cells and osteoclasts. The transcriptional activity of Mitf is repressed by HDAC7. Lastly, we show that either the amino or the carboxyl terminus of HDAC7 is sufficient for transcriptional repression and that the repression of HDAC7 is insensitive to trichostatin A, indicating that HDAC7 represses Mitf at least in part by deacetylation-independent mechanism.
引用
收藏
页码:12056 / 12065
页数:10
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