| Literature DB >> 26450370 |
Toru Fukuda1, Hiroki Ochi1, Satoko Sunamura1, Akina Haiden2, Waka Bando3, Hiroyuki Inose4, Atsushi Okawa5, Yoshinori Asou5, Shu Takeda6.
Abstract
Osteoblastic differentiation is regulated by various factors, including hormones and transcription factors. Runt-related transcription factor 2 (Runx2) is an essential player in osteoblastogenesis and transactivates its molecular target by creating a protein complex with its hetero-dimeric partner core binding factor beta (Cbfb). However, the molecular regulation of Cbfb expression remains unknown. Here, we identified miR-145 as a crucial regulator of Cbfb expression. The expression of miR-145 increased during osteoblastogenesis, indicating that miR-145 works as an inhibitor of osteoblastogenesis. Stable expression of miR-145 decreased endogenous Cbfb expression and inhibited osteoblastogenesis, in cooperation with miR-34c. Furthermore, miR-145 decreased bone regeneration in vivo. Our results indicate that miR-145 physiologically regulates osteoblast differentiation and bone formation via Cbfb expression by forming a regulatory microRNA network.Entities:
Keywords: Core binding factor beta; MicroRNA; Osteoblast
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Year: 2015 PMID: 26450370 DOI: 10.1016/j.febslet.2015.09.024
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124