Molecular mechanisms of adipocyte differentiation and inhibitory action of Pref-1

被引:51
作者
Smas, CM [1 ]
Sul, HS [1 ]
机构
[1] Univ Calif Berkeley, Dept Nutr Sci, Berkeley, CA 94720 USA
来源
CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION | 1997年 / 7卷 / 04期
关键词
adipocytes; differentiation; pref-1; EGF-like repeat; obesity; 3T3-L1; cells; growth factors; extracellular matrix;
D O I
10.1615/CritRevEukarGeneExpr.v7.i4.10
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Commitment and differentiation of adipocytes is governed by transcription factors that are under the control of the combinatorial effects of hormonal and cell-cell and cell-matrix interaction. Established preadipocyte cell lines, such as 3T3-L1, 3T3-F442A, and Ob 17, have made it possible to examine the molecular details of the differentiation process. Differentiation is accompanied by dramatic increases in adipocyte genes, including adipocyte fatty acid-binding protein and lipid-metabolizing enzymes. Transcription factors PPAR gamma and C/EBP have been shown to transactivate some of the adipocyte-expressed genes. By integrating hormonal and metabolic cues, these nuclear factors may synergistically function in adipocyte lineage determination and differentiation. Adipocyte differentiation involves drastic cell shape alterations that are accompanied by changes in expression of cytoskeletal and extracellular matrix proteins, including decreases in actin and tubulin levels. Pref-1, an EGF repeat containing transmembrane protein, is highly expressed in preadipocytes; this expression is totally abolished after differentiation to adipocytes. Pref-1 is inhibitory for adipocyte differentiation and processing of transmembrane pref-1 generates a biologically active soluble form corresponding to the ectodomain. Interaction of the EGF-repeats of pref-1 with an as yet unidentified receptor may mediate the inhibitory effects of pref-1 in adipocyte differentiation, thereby affecting nuclear events accompanying adipogenesis.
引用
收藏
页码:281 / 298
页数:18
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