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干扰素-γ对培养的人肾小球上皮细胞中C4基因表达的调控

Interferon-gamma regulation of C4 gene expression in cultured human glomerular epithelial cells.

作者信息

Zhou W, Campbell R D, Martin J, Sacks S H

机构信息

Renal Laboratory, United Medical School, Guy's Hospital, London, GB.

出版信息

Eur J Immunol. 1993 Oct;23(10):2477-81. doi: 10.1002/eji.1830231015.

Abstract

The fourth component of human complement is mainly produced in liver, but extrahepatic gene expression has been reported in human renal tissue and other tissues, and is thought to contribute to the inflammatory reaction in local tissue. To identify the cellular origin of C4 synthesis in human kidney, we studied C4 gene expression and regulation by interferon-gamma (IFN-gamma) and C4 protein biosynthesis in isolated glomerular epithelial cells. cDNA/polymerase chain reaction analysis showed that C4 transcripts are present in glomerular epithelial cells (GEC), and that gene expression is up-regulated by IFN-gamma. Metabolic labeling studies showed that GEC synthesize and secrete C4 as three polypeptide chains of approximately 90, 70, and 30 kDa, which correspond to the bands produced by hepatoma cells. These results suggest that the fourth component of complement is produced by GEC. The GEC has an important role in the maintenance of glomerular barrier function, which is lost in a number of complement-dependent conditions; glomerular epithelial synthesis of C4 could have a bearing on the possible physiological or pathological roles of complement under different circumstances.

摘要

人类补体的第四成分主要在肝脏中产生,但已有报道称其在人类肾脏组织和其他组织中有肝外基因表达,并且被认为在局部组织的炎症反应中起作用。为了确定人类肾脏中C4合成的细胞来源,我们研究了分离的肾小球上皮细胞中C4基因的表达以及干扰素-γ(IFN-γ)对其的调控作用和C4蛋白的生物合成。cDNA/聚合酶链反应分析表明,C4转录本存在于肾小球上皮细胞(GEC)中,并且基因表达受IFN-γ上调。代谢标记研究表明,GEC合成并分泌C4,其为三条分别约90、70和30 kDa的多肽链,这与肝癌细胞产生的条带相对应。这些结果表明补体的第四成分是由GEC产生的。GEC在维持肾小球屏障功能中起重要作用,而在许多补体依赖性疾病中该功能会丧失;肾小球上皮细胞合成C4可能与补体在不同情况下的生理或病理作用有关。

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