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前列腺素F2α刺激脂肪细胞前体中转化生长因子-α的表达。

Prostaglandin F2 alpha stimulates transforming growth factor-alpha expression in adipocyte precursors.

作者信息

Lepak N M, Serrero G

机构信息

W. Alton Jones Cell Science Center, Inc., Lake Placid, New York 12946, USA.

出版信息

Endocrinology. 1995 Aug;136(8):3222-9. doi: 10.1210/endo.136.8.7628355.

Abstract

Transforming growth factor-alpha (TGF alpha) and prostaglandin F2 alpha (PGF2 alpha) are potent inhibitors of adipocyte differentiation. We demonstrate here that TGF alpha messenger RNA (mRNA) is expressed in freshly isolated fat pads and in primary culture of adipocyte precursors cultivated in defined medium before and after differentiation. We show that PGF2 alpha stimulated TGF alpha mRNA expression in a dose-dependent manner. PGF2 alpha also stimulated TGF alpha production in the culture medium of adipocyte precursors in primary culture. PGF2 alpha stimulated TGF alpha mRNA expression in both undifferentiated and differentiated cells. 9 alpha,11 beta-PGF2 alpha, which also inhibited adipose differentiation, stimulated TGF alpha mRNA expression similarly to PGF2 alpha, whereas other PGs had no effect on TGF alpha mRNA expression. The time-course experiment indicates that the stimulation of TGF alpha mRNA expression by PGF2 alpha is observed within 6 h of exposure to PGF2 alpha and is inhibited by treatment of the cells with actinomycin D. The effect of PGF2 alpha on TGF alpha expression did not require activation of protein kinase C and was fully reversible. As both TGF alpha and PGF2 alpha are inhibitors of adipose differentiation, it is suggested that stimulation of TGF alpha expression by PGF2 alpha could represent an amplification mechanism to modulate adipocyte precursor differentiation and adipocyte function within the adipose tissue.

摘要

转化生长因子-α(TGFα)和前列腺素F2α(PGF2α)是脂肪细胞分化的强效抑制剂。我们在此证明,TGFα信使核糖核酸(mRNA)在新鲜分离的脂肪垫以及在分化前后于限定培养基中培养的脂肪细胞前体的原代培养物中均有表达。我们表明,PGF2α以剂量依赖性方式刺激TGFα mRNA表达。PGF2α还刺激原代培养的脂肪细胞前体培养基中TGFα的产生。PGF2α在未分化和分化的细胞中均刺激TGFα mRNA表达。9α,11β-前列腺素F2α同样抑制脂肪分化,其刺激TGFα mRNA表达的方式与PGF2α相似,而其他前列腺素对TGFα mRNA表达无影响。时间进程实验表明,在暴露于PGF2α后6小时内即可观察到PGF2α对TGFα mRNA表达的刺激作用,且放线菌素D处理细胞可抑制该作用。PGF2α对TGFα表达的影响不需要蛋白激酶C的激活,并且是完全可逆的。由于TGFα和PGF2α均为脂肪分化的抑制剂,因此提示PGF2α对TGFα表达的刺激可能代表一种放大机制,以调节脂肪组织内脂肪细胞前体的分化和脂肪细胞功能。

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