Regulation of CCAAT/enhancer binding proteinα (C/EBPα) gene expression by thiazolidinediones in 3T3-L1 adipocytes

被引:9
作者
Hemati, N [1 ]
Erickson, RL [1 ]
Ross, SE [1 ]
Liu, R [1 ]
MacDougald, OA [1 ]
机构
[1] Univ Michigan, Med Ctr, Dept Physiol, Ann Arbor, MI 48109 USA
关键词
D O I
10.1006/bbrc.1998.8204
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
Thiazolidinediones are a class of antidiabetic drugs that induce preadipocyte differentiation by binding and activating peroxisome proliferator-activated receptor gamma 2. Although thiazolidinediones are commonly thought of as insulin-sensitizing agents, these drugs have opposing and antagonistic effects to that of insulin on CCAAT/enhancer binding protein alpha (C/EBP alpha) gene expression in fully differentiated 3T3-L1 adipocytes. Thiazolidinediones induce expression of C/EBP alpha mRNA and protein, while insulin stimulates a rapid decline in C/EBP alpha mRNA and protein. When added in combination, thiazolidinediones block the suppression of C/EBP alpha mRNA by insulin; however, thiazolidinediones do not block the insulin-induced decline in GLUT4 mRNA indicating that repression of C/EBP alpha mRNA is not required for insulin to suppress expression of a C/EBP alpha-responsive gene such as GLUT4. Instead, insulin may regulate GLUT4 mRNA by inactivating C/EBP alpha through dephosphorylation as well as by inducing the expression of the dominant negative form of C/EBP beta (liver inhibitory protein), since both of these processes occur in the presence of thiazolidinediones. (C) 1998 Academic Press.
引用
收藏
页码:20 / 25
页数:6
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