Inhibition of preadipocyte differentiation by myostatin treatment in 3T3-L1 cultures

被引:119
作者
Kim, HS
Liang, L
Dean, RG
Hausman, DB
Hartzell, DL
Baile, CA
机构
[1] Univ Georgia, Dept Anim & Dairy Sci, Athens, GA 30602 USA
[2] Univ Georgia, Dept Foods & Nutr, Athens, GA 30602 USA
[3] MetaMorphix Inc, Baltimore, MD 21227 USA
关键词
myostatin; CCAAT/enhancer-binding protein alpha (C/EBP alpha); peroxisome proliferator-activated receptor gamma (PPAR gamma); 3T3-L1;
D O I
10.1006/bbrc.2001.4435
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
Myostatin, a new TGF-beta family member, is known as a muscle growth inhibitor, but its role in adipocyte development has not been studied. To test the role of Myostatin in 3T3-L1 preadipocyte differentiation, we treated cultured 3T3-L1 preadipocytes with Myostatin dissolved in 0.1% trifluoroacetic acid (TFA) during differentiation after they had become confluent. Myostatin treatment significantly decreased glycerol-3-phosphate dehydrogenase (GPDH) activity and oil Red-O staining compared to controls that did not receive Myostatin. Western blot analysis showed that the expression levels of CCAAT-enhancer binding protein a! (C/EBP alpha) and peroxisome proliferator-activated receptor gamma (PPAR gamma) were significantly decreased by Myostatin treatment (P < 0.05). However, the expression of C/EBP <beta> was not significantly changed by the treatment (P > 0.05). From RT-PCR result, the relative level of leptin mRNA in Myostatin-treated cells was not significantly different (P > 0.1) from the level in cells without Myostatin treatment. Our data show that Myostatin, a secreted protein from muscle, inhibits preadipocyte differentiation in 3T3-L1 cells, which is mediated, in part, by altered regulation of C/EBP a! and PPAR gamma. (C) 2001 Academic Press.
引用
收藏
页码:902 / 906
页数:5
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