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人肺成纤维细胞中转化生长因子-β的自诱导

Auto-induction of transforming growth factor-beta in human lung fibroblasts.

作者信息

Kelley J, Shull S, Walsh J J, Cutroneo K R, Absher M

机构信息

Department of Medicine, University of Vermont College of Medicine, Burlington 05405.

出版信息

Am J Respir Cell Mol Biol. 1993 Apr;8(4):417-24. doi: 10.1165/ajrcmb/8.4.417.

Abstract

The type beta transforming growth factors (TGF-beta s) are a family of potent cytokines with diverse effects on proliferation, differentiation, turnover of extracellular matrix components, oncogene expression, and other aspects of cellular phenotype. Unlike lung fibroblasts of certain species, unstimulated human lung fibroblast lines produce little or no TGF-beta in culture. However, TGF-beta has been reported to autoregulate its own production in certain human tumor cells and in rodent cell lines. To test whether this phenomenon is operative in fibroblasts from normal human lung tissue, confluent cultures of IMR90 normal fetal lung fibroblasts were exposed to TGF-beta. Cultures were exposed briefly to purified TGF-beta 1 under serum-free conditions and secretion of newly synthesized TGF-beta over the ensuing 72 h was determined by immunoblotting and bioassays made specific with the use of neutralizing antibodies. Steady-state levels of mRNA for TGF-beta 1 were detected by Northern and slot blot hybridization analysis of total cellular RNA. The 2.5 kb TGF-beta 1 mRNA species rose within 1.5 h of exposure of IMR90 cells to TGF-beta 1 and reached maximal levels after 16 h. Increased levels of TGF-beta were detected in conditioned medium 9 h after the start of the exposure. Thereafter, TGF-beta continued to accumulate at an elevated rate (90 +/- 7 versus < or = 15 pg/10(6) cells/h in uninduced cells) for up to 72 h. As little as 1 ng/ml TGF-beta 1 auto-induced TGF-beta secretion.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

β型转化生长因子(TGF-βs)是一类强效细胞因子,对细胞增殖、分化、细胞外基质成分的更新、癌基因表达及细胞表型的其他方面具有多种作用。与某些物种的肺成纤维细胞不同,未受刺激的人肺成纤维细胞系在培养中产生很少或不产生TGF-β。然而,据报道TGF-β在某些人类肿瘤细胞和啮齿动物细胞系中可自动调节自身的产生。为了测试这种现象在正常人肺组织来源的成纤维细胞中是否起作用,将IMR90正常胎儿肺成纤维细胞的汇合培养物暴露于TGF-β。在无血清条件下将培养物短暂暴露于纯化的TGF-β1,并通过免疫印迹和使用中和抗体进行的生物测定来确定在随后72小时内新合成的TGF-β的分泌情况。通过对总细胞RNA进行Northern和狭缝印迹杂交分析来检测TGF-β1的mRNA稳态水平。IMR90细胞暴露于TGF-β1后1.5小时内,2.5 kb的TGF-β1 mRNA种类增加,并在16小时后达到最高水平。暴露开始9小时后,在条件培养基中检测到TGF-β水平升高。此后,TGF-β继续以升高的速率积累(90±7与未诱导细胞中≤15 pg/10(6)细胞/小时相比),长达72小时。低至1 ng/ml的TGF-β1可自动诱导TGF-β分泌。(摘要截短于250字)

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