| Literature DB >> 27300495 |
Ping Zhang1,2, Yunsong Liu1, Chanyuan Jin1, Min Zhang1, Longwei Lv1, Xiao Zhang1, Hao Liu1, Yongsheng Zhou3,4.
Abstract
Human mesenchymal stem cells (MSCs) are multipotent progenitor cells that can differentiate into osteoblasts, chondrocytes, and adipocytes. The importance of epigenetic regulation for osteogenic differentiation of MSCs is widely accepted. However, the molecular mechanisms are poorly understood. Here, we show that histone H3K9 acetyltransferase PCAF plays a critical role in osteogenic differentiation of MSCs. Knockdown of PCAF significantly reduced the bone formation both in vitro and in vivo. Mechanistically, PCAF controls BMP signaling genes expression by increasing H3K9 acetylation. Most importantly, PCAF expression is significantly decreased in bone sections of ovariectomized or aged mice. Histone modification enzyme is chemically modifiable; therefore, PCAF may represent a novel therapeutic target for stem cell-mediated regenerative medicine and the treatment of osteoporosis. Stem Cells 2016;34:2332-2341.Entities:
Keywords: Bone morphogenetic protein; H3K9 acetylation; Osteogenic differentiation; Osteoporosis; P300/CBP-associated factor
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Year: 2016 PMID: 27300495 DOI: 10.1002/stem.2424
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277