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Crry的过表达可保护系膜细胞免受补体介导的损伤。

Overexpression of Crry protects mesangial cells from complement-mediated injury.

作者信息

Nangaku M, Quigg R J, Shankland S J, Okada N, Johnson R J, Couser W G

机构信息

Division of Nephrology, University of Washington, Seattle 98195-6521, USA.

出版信息

J Am Soc Nephrol. 1997 Feb;8(2):223-33. doi: 10.1681/ASN.V82223.

Abstract

Crry is a membrane-associated complement regulatory protein expressed on glomerular mesangial, endothelial, and epithelial cells, which reduces C3/C5 convertase activity. This study utilized an overexpression strategy to determine the functional significance of Crry in cultured rat mesangial cells. A Crry expression vector was constructed and was tagged with a c-myc epitope that allowed transfected Crry to be distinguished from the constitutively expressed protein. In stable clones, overexpressed Crry was clearly detected immunocytochemically both by anti-c-myc and anti-Crry antibody in a membrane localization. The overexpression of Crry was also confirmed by Western blotting and immunoprecipitation. To determine if overexpression of Crry by mesangial cells confers a protective effect from complement attack, complement-mediated cell lysis assays were performed. Crry-transfected mesangial cells demonstrated complete resistance to complement-mediated cell lysis, which was reversed by neutralization of Crry with both monoclonal antibody and F(ab')2 fragments of the antibody. This study also investigated the role of Crry in protecting cells from the effects of sublytic complement attack. Overexpressed Crry suppressed antibody/complement induced production of superoxide, one of the inflammatory mediators induced by sublytic complement attack. Immunocytochemical staining confirmed a reduction in C3 and C5b-9 deposition in Crry-transfected cells. These results demonstrate directly that transfected Crry functions as a potent protector of mesangial cells against complement-mediated injury. Crry may play an important role in modulating the glomerular response to immune injury in vivo.

摘要

Crry是一种在肾小球系膜细胞、内皮细胞和上皮细胞上表达的膜相关补体调节蛋白,它可降低C3/C5转化酶的活性。本研究采用过表达策略来确定Crry在培养的大鼠系膜细胞中的功能意义。构建了一个Crry表达载体,并标记了一个c-myc表位,使得转染的Crry能够与组成型表达的蛋白区分开来。在稳定克隆中,通过抗c-myc和抗Crry抗体在膜定位上均能通过免疫细胞化学清晰检测到过表达的Crry。Crry的过表达也通过蛋白质印迹法和免疫沉淀法得到证实。为了确定系膜细胞中Crry的过表达是否赋予对补体攻击的保护作用,进行了补体介导的细胞裂解试验。转染Crry的系膜细胞对补体介导的细胞裂解表现出完全抗性,用单克隆抗体和该抗体的F(ab')2片段中和Crry可逆转这种抗性。本研究还调查了Crry在保护细胞免受亚溶细胞性补体攻击影响中的作用。过表达的Crry抑制了抗体/补体诱导的超氧化物产生,超氧化物是亚溶细胞性补体攻击诱导的炎症介质之一。免疫细胞化学染色证实转染Crry的细胞中C3和C5b-9沉积减少。这些结果直接表明转染的Crry作为系膜细胞对抗补体介导损伤的有效保护剂发挥作用。Crry可能在调节体内肾小球对免疫损伤的反应中起重要作用。

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