首页> 外文期刊>Journal of Pathology: Journal of the Pathological Society of Great Britain and Ireland >Role of mesangial Factor V expression in crescent formation in rat experimental mesangioproliferative glomerulonephritis.
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Role of mesangial Factor V expression in crescent formation in rat experimental mesangioproliferative glomerulonephritis.

机译:肾小球系膜因子V表达在大鼠实验性血管增生性肾小球肾炎的新月形成中的作用。

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It has been suggested that fibrin deposition participates in the development of crescents in active glomerulonephritis (GN). In human IgA nephropathy, which is a common form of mesangioproliferative GN (MsPGN), crescent formation is occasionally observed in active disease, leading to end-stage renal failure. Factor V is a membrane-bound potent cofactor for the conversion of prothrombin to thrombin by Factor Xa. An in vivo study was conducted to clarify the contribution of local fibrin production to crescent formation in MsPGN through mesangial Factor V expression. Wistar rats were injected intravenously with rabbit anti-rat thymocyte serum. Three days after injection, mesangiolysis with intense mesangial Factor V expression was observed and immunoelectron microscopy revealed fibrin localization in mesangiolytic lesions, which had spread into the glomerular basement membrane adjacent to the destroyed mesangium, accompanied by clots in Bowman's space. Marked glomerular fibrin deposition, together with its deposition in Bowman's space and cellular crescent formation, was noted with mesangial proliferation on day 8. Specific bands for Factor V mRNA were also detected from isolated glomeruli. Fibrin deposition and cellular crescent formation were significantly suppressed by treatment with anti-Factor V antibody. These results suggest that local fibrin production, following mesangial Factor V expression, together with mesangiolysis that spreads to the adjacent glomerular basement membrane, plays a role in crescent formation in MsPGN.
机译:已经提出,纤维蛋白沉积参与活动性肾小球肾炎(GN)中新月形的发展。在人IgA肾病中,它是血管增生性GN(MsPGN)的常见形式,在活动性疾病中偶尔会观察到新月形形成,从而导致晚期肾衰竭。因子V是通过因子Xa将凝血酶原转化为凝血酶的膜结合有效辅因子。进行了一项体内研究,以阐明局部纤维蛋白通过肾小球膜因子V表达对MsPGN中新月形形成的贡献。向Wistar大鼠静脉内注射兔抗大鼠胸腺细胞血清。注射后三天,观察到具有强烈的肾小球系膜因子V表达的血管溶解,免疫电子显微镜检查显示纤维蛋白位于血管溶解性病变中,并已扩散到与被破坏的血管系膜相邻的肾小球基底膜中,并伴有鲍曼腔内的血凝块。在第8天,随着肾小球系膜增生,注意到了明显的肾小球纤维蛋白沉积,以及其在鲍曼氏腔中的沉积和细胞新月形的形成。纤维蛋白沉积和细胞月牙形成被抗因子V抗体治疗显着抑制。这些结果表明,肾小球膜因子V表达后,局部血纤蛋白的产生,以及扩散到邻近肾小球基底膜的血管溶解作用,在MsPGN的新月形成中起作用。

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