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衰变加速因子调节肾小球上皮细胞上的补体激活。

Decay accelerating factor regulates complement activation on glomerular epithelial cells.

作者信息

Quigg R J, Nicholson-Weller A, Cybulsky A V, Badalamenti J, Salant D J

机构信息

Evans Memorial Department of Clinical Research, University Hospital, Boston, MA 02118.

出版信息

J Immunol. 1989 Feb 1;142(3):877-82.

PMID:2464030
Abstract

Epithelial cells of the glomerular capillary are the site of C5b-9 mediated injury in rat membranous nephropathy. We investigated the regulation of C activation by cultured glomerular epithelial cells (GEC). Rat and human GEC were more resistant to C injury by homologous C than heterologous C. In human GEC homologous C cytotoxicity was enhanced by antiserum to decay accelerating factor (DAF) indicating that homologous C activation was, at least in part, restricted by membrane DAF. Anti-DAF immunoprecipitated a 67-kDa protein from human glomeruli. In rat GEC, pronase and phosphatidylinositol-specific phospholipase C (which are known to inactivate human DAF) enhanced cytotoxicity by homologous C. Thus, DAF is present on human GEC in culture and in human kidney glomeruli, and a DAF-like protein is present on cultured rat GEC. These proteins regulate C activation in vitro and may play a role in controlling C activation on GEC in vivo.

摘要

肾小球毛细血管的上皮细胞是大鼠膜性肾病中C5b - 9介导损伤的部位。我们研究了培养的肾小球上皮细胞(GEC)对补体(C)激活的调节作用。大鼠和人GEC对同源补体损伤的抵抗能力强于异源补体。在人GEC中,抗衰变加速因子(DAF)抗血清可增强同源补体的细胞毒性,表明同源补体激活至少部分受膜DAF的限制。抗DAF从人肾小球中免疫沉淀出一种67 kDa的蛋白质。在大鼠GEC中,链霉蛋白酶和磷脂酰肌醇特异性磷脂酶C(已知可使人类DAF失活)增强了同源补体的细胞毒性。因此,DAF存在于培养的人GEC和人肾小球中,并且一种类似DAF的蛋白质存在于培养的大鼠GEC中。这些蛋白质在体外调节补体激活,可能在体内控制GEC上的补体激活中发挥作用。

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