Inhibitor of DNA Binding 4 (ID4) Regulation of Adipocyte Differentiation and Adipose Tissue Formation in Mice

被引:23
作者
Murad, Joana M.
Place, Chelsea S.
Ran, Cong
Hekmatyar, Shahryar K. N. [3 ]
Watson, Nathan P.
Kauppinen, Risto A. [3 ]
Israel, Mark A. [1 ,2 ]
机构
[1] Dartmouth Med Sch, Dept Pediat, Hanover, NH 03755 USA
[2] Dartmouth Med Sch, Dept Genet, Hanover, NH 03755 USA
[3] Dartmouth Med Sch, Dept Radiol, Hanover, NH 03755 USA
关键词
PPAR-GAMMA; C/EBP-ALPHA; INSULIN-RESISTANCE; EXPRESSION; ADIPOGENESIS; LIPODYSTROPHY; PROTEINS;
D O I
10.1074/jbc.M110.128744
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
Inhibitor of DNA binding 4 (ID4) is a helix-loop-helix protein that heterodimerizes with basic helix-loop-helix transcription factors inhibiting their function. ID4 expression is important for adipogenic differentiation of the 3T3-L1 cell line, and inhibition of ID4 is associated with a concomitant decrease in CCAAT/enhancer-binding protein gamma and peroxisome proliferator-activated receptor gamma mRNA and protein expression. Mice with a homozygous deletion of Id4 (Id4(-/-)) have reduced body fat and gain much less weight compared with wild-type littermates when placed on diets with high fat content. Mouse embryonic fibroblasts (MEFs) isolated from Id4(-/-) mice have reduced adipogenic potential when compared with wild-type MEFs. In agreement with changes in morphological differentiation, the levels of CCAAT/enhancer-binding protein alpha and peroxisome proliferator-activated receptor gamma were also reduced in MEFs from Id4(-/-) mice. Our results demonstrate the importance of ID4 in adipocyte differentiation and the implications of this regulation for adipose tissue formation.
引用
收藏
页码:24164 / 24173
页数:10
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