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大肠杆菌志贺毒素与人小儿肾小球系膜细胞的结合

Escherichia coli verotoxin binding to human paediatric glomerular mesangial cells.

作者信息

Robinson L A, Hurley R M, Lingwood C, Matsell D G

机构信息

Department of Paediatrics, University of Western Ontario, London, Canada.

出版信息

Pediatr Nephrol. 1995 Dec;9(6):700-4. doi: 10.1007/BF00868715.

Abstract

Haemolytic uraemic syndrome (HUS) remains the leading cause of acute renal failure in children. Although an Escherichia coli-produced verotoxin (VT) has been implicated in the pathogenesis of HUS, the precise mechanisms of disease are not well defined. We hypothesise that the pathogenesis of renal failure in HUS includes the binding of E. coli VT to the glomerular mesangial cell, with consequent effects on renal function. Using human paediatric mesangial cells, we studied the binding and biological effects of the purified verotoxin VT-1. We isolated, purified and characterised paediatric glomerular mesangial cells. The mesangial cells were characterised by their immunoreactivity with both smooth muscle actin and vimentin antibodies, and lack of immunoreactivity with cytokeratin or factor VIII antibodies. Using an fluorescein isothiocyanate-conjugated VT (10(-7)-10(-8) M), we demonstrated specific binding to the mesangial cell membrane by immunofluorescence microscopy. We also demonstrated a dose-dependent inhibition of mesangial cell mitogenesis at concentrations from 10(-9) to 10(-17) M. Our data demonstrate that VT-1 binds to paediatric human glomerular mesangial cells and this binding results in specific biological actions, including an inhibition of cell mitogenesis.

摘要

溶血尿毒综合征(HUS)仍是儿童急性肾衰竭的主要病因。尽管一种大肠杆菌产生的志贺毒素(VT)被认为与HUS的发病机制有关,但确切的疾病机制尚不清楚。我们推测,HUS中肾衰竭的发病机制包括大肠杆菌VT与肾小球系膜细胞的结合,从而对肾功能产生影响。我们使用人小儿系膜细胞,研究了纯化的志贺毒素VT-1的结合及生物学效应。我们分离、纯化并鉴定了小儿肾小球系膜细胞。系膜细胞的特征是与平滑肌肌动蛋白和波形蛋白抗体均有免疫反应性,而与细胞角蛋白或因子VIII抗体无免疫反应性。使用异硫氰酸荧光素偶联的VT(10^-7 - 10^-8 M),我们通过免疫荧光显微镜证明了其与系膜细胞膜的特异性结合。我们还证明,在10^-9至10^-17 M的浓度范围内,系膜细胞有丝分裂受到剂量依赖性抑制。我们的数据表明,VT-1与人小儿肾小球系膜细胞结合,这种结合导致特定的生物学作用,包括抑制细胞有丝分裂。

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