期刊
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
卷 488, 期 2, 页码 91-99出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.abb.2009.07.007
关键词
Metadoxine; Adipogenesis; Protein kinase A; cAMP response element binding protein; CCAAT/enhancer-binding protein beta
资金
- Seoul RBD Program
Adipogenesis is orchestrated by the expression of master adipogenic regulators. In particular, phosphorylation of cAMP response element binding protein (CREB) by protein kinase A promotes CREB nuclear translocation, thereby inducing expression of the adipogenic regulators and resulting in adipogenic maturation. Although metadoxine, an ion-pair of pyridoxine and L-2-pyrrolidone-5-carboxylate, has been shown to inhibit lipid accumulation in the liver, its effect on adipocyte differentiation has never been explored. This study investigated the effects of metadoxine on the differentiation of 3T3-L1 preadipocytes and the molecular mechanism. Metadoxine treatment did not inhibit mitotic clonal expansion, but inhibited late-stage cell differentiation, suggesting that metadoxine may block the differentiation step of preadipocytes. Metadoxine inhibited CREB phosphorylation and binding to the cAMP response element, thereby repressing CCAAT/enhancer-binding protein beta during hormone-induced adipogenesis. Overall, metadoxine inhibits adipogenic differentiation in association with the inhibition of CREB/cAMP response element-dependent CCAAT/enhancer-binding protein b induction in the protein kinase A-CREB pathway. (C) 2009 Elsevier Inc. All rights reserved.
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