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转化生长因子β(TGF-β)抑制原代培养的人脂肪细胞前体细胞的分化。

Transforming growth factor beta (TGF-beta) inhibits the differentiation of human adipocyte precursor cells in primary culture.

作者信息

Petruschke T, Röhrig K, Hauner H

机构信息

Diabetes Research Institute, Heinrich-Heine University Düsseldorf, Germany.

出版信息

Int J Obes Relat Metab Disord. 1994 Aug;18(8):532-6.

PMID:7951472
Abstract

In order to improve our understanding of the control of adipose tissue development in man by adipogenic and antiadipogenic factors we studied the effect of transforming growth factor beta (TGF beta) on the differentiation of human adipocyte precursor cells cultured in a serum-free medium. Addition of TGF beta at concentrations ranging from 5 to 100 pmol/l for 24 h at the beginning of the differentiation process resulted in a dose-dependent reduced expression of glycero-3-phosphate dehydrogenase (GPDH) activity. Continuous exposure of cells to TGF beta completely blocked differentiation even at a concentration of 5 pmol/l. Under these conditions cells were not able to accumulate lipid droplets. This inhibitory effect of TGF beta was not mediated by stimulation of cell proliferation. Exposure of newly developed fat cells to TGF beta was also associated with a significant suppression of GPDH activity. A 10-day incubation of cells with TGF beta reduced GPDH activity by more than 80% compared to controls. Despite this suppressive effect cells retained the typical fat cell-like morphology. In conclusion, these data clearly suggest that TGF beta exerts an inhibitory action on human adipose tissue development and reduces the activity of a lipogenic key enzyme in newly formed fat cells.

摘要

为了增进我们对成脂因子和抗成脂因子对人体脂肪组织发育调控的理解,我们研究了转化生长因子β(TGFβ)对在无血清培养基中培养的人脂肪细胞前体细胞分化的影响。在分化过程开始时添加浓度为5至100 pmol/l的TGFβ24小时,导致甘油-3-磷酸脱氢酶(GPDH)活性的表达呈剂量依赖性降低。即使在5 pmol/l的浓度下,细胞持续暴露于TGFβ也会完全阻断分化。在这些条件下,细胞无法积累脂滴。TGFβ的这种抑制作用不是由细胞增殖的刺激介导的。新形成的脂肪细胞暴露于TGFβ也与GPDH活性的显著抑制有关。与对照组相比,细胞与TGFβ孵育10天可使GPDH活性降低80%以上。尽管有这种抑制作用,细胞仍保持典型的脂肪细胞样形态。总之,这些数据清楚地表明,TGFβ对人体脂肪组织发育具有抑制作用,并降低新形成脂肪细胞中一种生脂关键酶的活性。

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