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脂肪酸对磷酸烯醇式丙酮酸羧激酶基因表达的刺激作用。

Stimulation of phosphoenolpyruvate carboxykinase gene expression by fatty acids.

作者信息

Antras-Ferry J, Le Bigot G, Robin P, Robin D, Forest C

机构信息

Centre de Recherche sur l'Endocrinologie Moléculaire et le Développement, C.N.R.S., Meudon, France.

出版信息

Biochem Biophys Res Commun. 1994 Aug 30;203(1):385-91. doi: 10.1006/bbrc.1994.2194.

Abstract

We used the 3T3-F442A adipocytes and the FAO hepatoma cells to analyze the effect of oleate on phosphoenolpyruvate carboxykinase (PEPCK) gene expression. In serum-deprived, glucose-free medium, 1 mM oleate, bound to albumin in a 6:1 ratio, specifically stimulated PEPCK mRNA. In 3T3-F442A adipocytes, the maximum 5-fold increase occurred in 4 hours then rapidly declined to reach the basal level 20 hours later. This increase was cycloheximide-independent and actinomycin D-dependent, suggesting a direct, transcriptional effect of oleate. FAO cells also responded to oleate with a transient induction of PEPCK mRNA, although the extent of stimulation was lower. Thus, the PEPCK gene provides a useful molecular tool for studying the mechanisms by which fatty acids stimulate gene expression.

摘要

我们使用3T3-F442A脂肪细胞和FAO肝癌细胞来分析油酸对磷酸烯醇式丙酮酸羧激酶(PEPCK)基因表达的影响。在无血清、无糖培养基中,以6:1的比例与白蛋白结合的1 mM油酸特异性地刺激了PEPCK mRNA。在3T3-F442A脂肪细胞中,4小时内出现最大5倍的增加,然后迅速下降,20小时后达到基础水平。这种增加不依赖于放线菌酮,而依赖于放线菌素D,表明油酸具有直接的转录作用。FAO细胞对油酸也有反应,PEPCK mRNA短暂诱导,尽管刺激程度较低。因此,PEPCK基因是研究脂肪酸刺激基因表达机制的有用分子工具。

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