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3',5'-环磷酸腺苷和佛波酯诱导绒毛膜癌细胞中转化生长因子-β1信使核糖核酸水平。

Adenosine 3',5'-monophosphate and phorbol ester induce transforming growth factor-beta 1 messenger ribonucleic acid levels in choriocarcinoma cells.

作者信息

Ritvos O, Erämaa M

机构信息

Department of Pathology, University of Helsinki, Finland.

出版信息

Endocrinology. 1991 Oct;129(4):2240-5. doi: 10.1210/endo-129-4-2240.

Abstract

Transforming growth factor-beta 1 (TGF-beta 1), a regulator of growth and differentiation of many cell types, has previously been purified from the human placenta, and the messenger (m) RNA is abundantly expressed there. We found that the approximate 2.5-kilobase TGF-beta 1 mRNA is expressed in JEG-3 human choriocarcinoma cells, which have been widely used as a model system for studying the regulation of trophoblast hormone secretion. Cholera toxin (CT) elevates the cellular levels of the second messenger cAMP and increases the secretion of CG and steroids in these cells, thus being a potent inducer of trophoblast-differentiated functions. We show that CT also stimulates TGF-beta 1 mRNA levels in JEG-3 cells in a concentration- and time-dependent manner as studied by Northern and dot blotting. The maximal effect (about 5-fold increase above basal levels) occurs within 12-48 h of induction with a CT concentration of 1.0 ng/ml. The cell-permeable cAMP-analog 8-bromo-cAMP stimulates the accumulation of TGF-beta 1 mRNA in JEG-3 cells as well. Furthermore, this cAMP analog also induces TGF-beta 1 mRNA levels in normal cultured term placental cytotrophoblasts. 12-O-Tetradecanoyl phorbol-13-acetate, an active phorbol ester protein kinase C regulator and inducer of TGF-beta 1 mRNA in many cells, increases TGF-beta 1 mRNA accumulation in JEG-3 cells with a similar time course as cAMP analogs but to a lesser extent. Human HT-1080 fibrosarcoma and A-549 lung carcinoma cells exhibit up-regulation of TGF-beta 1 mRNA in response to TGF-beta 1 itself, but we show that activation of the cAMP-dependent pathway does not affect TGF-beta 1 mRNA levels in these cells. Cycloheximide, an inhibitor of protein synthesis, prevents the effect of CT and 12-O-tetradecanoyl phorbol-13-acetate on TGF-beta 1 mRNA expression in JEG-3 cells, suggesting that a protein mediator may be involved in the transduction of their effects. Our finding of a cAMP-dependent induction pathway for TGF-beta 1 mRNA expression in JEG-3 cells provides a new mechanism for the regulation of the synthesis of this ubiquitous growth and differentiation factor and suggests that TGF-beta 1 may have a role in trophoblast differentiation.

摘要

转化生长因子-β1(TGF-β1)是多种细胞类型生长和分化的调节因子,此前已从人胎盘中纯化出来,其信使核糖核酸(mRNA)在胎盘中大量表达。我们发现,约2.5千碱基的TGF-β1 mRNA在JEG-3人绒毛膜癌细胞中表达,该细胞已被广泛用作研究滋养层激素分泌调节的模型系统。霍乱毒素(CT)可提高第二信使环磷酸腺苷(cAMP)的细胞水平,并增加这些细胞中绒毛膜促性腺激素(CG)和类固醇的分泌,因此是滋养层分化功能的有效诱导剂。我们通过Northern印迹法和斑点印迹法研究表明,CT还以浓度和时间依赖性方式刺激JEG-3细胞中TGF-β1 mRNA水平。在1.0 ng/ml的CT诱导12 - 48小时内出现最大效应(比基础水平增加约5倍)。细胞可渗透的cAMP类似物8-溴-cAMP也刺激JEG-3细胞中TGF-β1 mRNA的积累。此外,这种cAMP类似物还诱导正常培养的足月胎盘细胞滋养层细胞中TGF-β1 mRNA水平。12-O-十四烷酰佛波醇-13-乙酸酯是一种活性佛波醇酯蛋白激酶C调节剂,也是许多细胞中TGF-β1 mRNA的诱导剂,它增加JEG-3细胞中TGF-β1 mRNA的积累,其时间进程与cAMP类似物相似,但程度较小。人HT-1080纤维肉瘤细胞和A-549肺癌细胞对TGF-β1自身有反应,表现为TGF-β1 mRNA上调,但我们表明cAMP依赖性途径的激活并不影响这些细胞中TGF-β1 mRNA水平。蛋白质合成抑制剂放线菌酮可阻止CT和12-O-十四烷酰佛波醇-13-乙酸酯对JEG-3细胞中TGF-β1 mRNA表达的影响,这表明一种蛋白质介质可能参与其效应的转导。我们在JEG-3细胞中发现TGF-β1 mRNA表达的cAMP依赖性诱导途径,为调节这种普遍存在的生长和分化因子的合成提供了一种新机制,并表明TGF-β1可能在滋养层分化中起作用。

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