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纤连蛋白对3T3脂肪细胞形态及脂肪生成基因表达的调节作用

Fibronectin modulation of cell shape and lipogenic gene expression in 3T3-adipocytes.

作者信息

Spiegelman B M, Ginty C A

出版信息

Cell. 1983 Dec;35(3 Pt 2):657-66. doi: 10.1016/0092-8674(83)90098-3.

Abstract

The differentiation of 3T3-F442A cells is accompanied by changes in cell morphology, decreased synthesis and assembly of cytoskeletal proteins, and increased biosynthesis of lipogenic enzymes. The differentiation-dependent alterations in actin assembly can be prevented by culture of cells on fibronectin matrices. Under these conditions, morphological change is prevented and the induction of lipogenic enzymes such as glycerophosphate dehydrogenase and fatty acid synthetase is sharply reduced. In contrast, the differentiation-linked decreases in actin and tubulin biosynthesis occur normally. Hybridization of cytoplasmic and nuclear RNA to cloned cDNA probes indicates that the inhibition of lipogenic protein biosynthesis occurs because of reduced levels of specific mRNA production. The inhibitory effects of fibronectin can be reversed by keeping cells in a rounded configuration or by exposing cells to either cytochalasin D, which disrupts the actin cytoskeleton, or insulin, a key lipogenic hormone. These results demonstrate that fibronectin can regulate gene expression for lipogenic proteins and they suggest that it interferes with cytoskeletal and morphological changes necessary for new gene expression.

摘要

3T3 - F442A细胞的分化伴随着细胞形态的改变、细胞骨架蛋白合成与组装的减少以及生脂酶生物合成的增加。纤连蛋白基质上培养细胞可防止肌动蛋白组装中依赖分化的改变。在这些条件下,形态变化被阻止,甘油磷酸脱氢酶和脂肪酸合成酶等生脂酶的诱导显著降低。相反,与分化相关的肌动蛋白和微管蛋白生物合成的减少正常发生。细胞质和细胞核RNA与克隆的cDNA探针杂交表明,生脂蛋白生物合成的抑制是由于特定mRNA产生水平降低所致。通过使细胞保持圆形形态,或将细胞暴露于破坏肌动蛋白细胞骨架的细胞松弛素D或关键生脂激素胰岛素,纤连蛋白的抑制作用可被逆转。这些结果表明纤连蛋白可调节生脂蛋白的基因表达,并且提示它干扰新基因表达所需的细胞骨架和形态变化。

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