| Literature DB >> 25683718 |
Masatoshi Takagi1, Hatsume Uno2, Rina Nishi3, Masataka Sugimoto4, Setsuko Hasegawa3, Jinhua Piao3, Norimasa Ihara5, Sayaka Kanai6, Saori Kakei7, Yoshifumi Tamura7, Takayoshi Suganami8, Yasutomi Kamei9, Toshiaki Shimizu10, Akio Yasuda4, Yoshihiro Ogawa6, Shuki Mizutani3.
Abstract
Ataxia-telangiectasia (A-T) patients occasionally develop diabetes mellitus. However, only limited attempts have been made to gain insight into the molecular mechanism of diabetes mellitus development in A-T patients. We found that Atm-/- mice were insulin resistant and possessed less subcutaneous adipose tissue as well as a lower level of serum adiponectin than Atm+/+ mice. Furthermore, in vitro studies revealed impaired adipocyte differentiation in Atm-/- cells caused by the lack of induction of C/EBPα and PPARγ, crucial transcription factors involved in adipocyte differentiation. Interestingly, ATM was activated by stimuli that induced differentiation, and the binding of ATM to C/EBPβ and p300 was involved in the transcriptional regulation of C/EBPα and adipocyte differentiation. Thus, our study sheds light on the poorly understood role of ATM in the pathogenesis of glucose intolerance in A-T patients and provides insight into the role of ATM in glucose metabolism.Entities:
Year: 2015 PMID: 25683718 DOI: 10.1016/j.celrep.2015.01.027
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423