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转化生长因子-β对细胞因子产生的调节作用。

Modulation of cytokine production by transforming growth factor-beta.

作者信息

Chantry D, Turner M, Abney E, Feldmann M

机构信息

Charing Cross Sunley Research Center, London, England.

出版信息

J Immunol. 1989 Jun 15;142(12):4295-300.

PMID:2542408
Abstract

Transforming growth factor-beta 1 (TGF-beta 1) is one of a family of polypeptides involved in the regulation of cell growth and differentiation. The effects of human rTGF-beta 1 on the production of IL-1 and TNF by activated PBMC were studied. The addition of TGF-beta 1 alone caused an increase in the levels of mRNA for IL-1 alpha, IL-1 beta, and TGF-alpha. This was due to increased transcription rather than enhanced mRNA stability. The induced mRNA were of the appropriate size as assessed by Northern blotting. However, the mRNA did not appear to be translated into protein, inasmuch as the translation products of IL-1 beta and TNF-alpha were not detected by RIA or ELISA. Furthermore, in experiments utilizing a neutralizing antibody to TGF-beta 1, we were unable to unmask IL-1 biologic activities and unable to detect TNF biologic activity in the WEHI 164 cytotoxicity assay. TGF-beta inhibited in a dose-dependent manner the induction of IL-1 beta by LPS or TNF but not by PHA and PMA. Similarly, LPS induction of TNF-alpha was blocked by TGF-beta, whereas induction of PMA and PHA was completely resistant. TGF-beta 1 did not increase PGE2 secretion or cause elevated intracellular cAMP; thus, the inhibitory effects of TGF-beta 1 seem not to be mediated by PGE2 or cAMP, which have both been implicated in post-transcriptional control of cytokine gene expression. These findings suggest a dual role for TGF-beta 1 in the regulation of cytokine production at both transcriptional and translational levels.

摘要

转化生长因子-β1(TGF-β1)是参与细胞生长和分化调节的多肽家族之一。研究了重组人TGF-β1对活化的外周血单个核细胞(PBMC)产生白细胞介素-1(IL-1)和肿瘤坏死因子(TNF)的影响。单独添加TGF-β1会导致IL-1α、IL-1β和TGF-α的mRNA水平升高。这是由于转录增加而非mRNA稳定性增强所致。通过Northern印迹法评估,诱导产生的mRNA大小合适。然而,这些mRNA似乎并未翻译成蛋白质,因为通过放射免疫分析(RIA)或酶联免疫吸附测定(ELISA)未检测到IL-1β和TNF-α的翻译产物。此外,在使用抗TGF-β1中和抗体的实验中,我们无法揭示IL-1的生物学活性,并且在WEHI 164细胞毒性试验中无法检测到TNF的生物学活性。TGF-β以剂量依赖的方式抑制LPS或TNF诱导的IL-1β产生,但不抑制PHA和PMA诱导的IL-1β产生。同样,TGF-β阻断LPS诱导的TNF-α产生,而对PMA和PHA诱导的TNF-α产生完全无抑制作用。TGF-β1不会增加前列腺素E2(PGE2)的分泌,也不会导致细胞内cAMP升高;因此,TGF-β1的抑制作用似乎不是由PGE2或cAMP介导的,而PGE2和cAMP都与细胞因子基因表达的转录后调控有关。这些发现表明TGF-β1在转录和翻译水平上对细胞因子产生的调节中具有双重作用。

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