Amri E Z, Bertrand B, Ailhaud G, Grimaldi P
Centre de Biochimie (CNRS-UMR 134), U.F.R. Sciences, Université de Nice-Sophia Antipolis, France.
J Lipid Res. 1991 Sep;32(9):1449-56.
The regulation of the expression of adipose-related genes, i.e., aP2, adipsin, and glycerophosphate dehydrogenase (GPDH) by growth hormone (GH) and polyamines, as well as the role of fatty acids, have been investigated in polyamine-dependent Ob1754 cells and Ob1771 preadipose cells. Growth hormone acts as an obligatory hormone for adipsin and GPDH gene expression but its presence is not required for the expression of the aP2 gene. In fully differentiated Ob1771 cells, impairment of fatty acid synthesis by glucose deprivation leads to an inhibition of the aP2 gene expression, whereas the expression of adipsin and GPDH genes remains unaffected. Supplementation of the culture medium with fatty acids prevents the decrease of aP2 gene expression, and this effect appears primarily due to an increase in the transcriptional level of aP2 gene. The induction of aP2 gene has been examined in early committed, lipid-free Ob1771 cells in which fatty acid synthesis is very low despite glucose supplementation. Long-chain fatty acids (greater than or equal to C12) are able to activate the aP2 gene. It is concluded that fatty acids or fatty acid metabolites activate the aP2 gene and subsequently modulate its expression.
在多胺依赖性的Ob1754细胞和Ob1771前脂肪细胞中,研究了生长激素(GH)和多胺对脂肪相关基因,即aP2、脂肪酶和甘油磷酸脱氢酶(GPDH)表达的调节作用,以及脂肪酸的作用。生长激素是脂肪酶和GPDH基因表达所必需的激素,但aP2基因的表达并不需要生长激素的存在。在完全分化的Ob1771细胞中,葡萄糖剥夺导致脂肪酸合成受损,进而抑制aP2基因的表达,而脂肪酶和GPDH基因的表达则不受影响。向培养基中添加脂肪酸可防止aP2基因表达的降低,这种作用主要是由于aP2基因转录水平的增加。在早期定向分化、无脂质的Ob1771细胞中检测了aP2基因的诱导情况,尽管添加了葡萄糖,这些细胞中的脂肪酸合成仍然很低。长链脂肪酸(大于或等于C12)能够激活aP2基因。得出的结论是,脂肪酸或脂肪酸代谢产物激活aP2基因并随后调节其表达。