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糖尿病肾小球中胶原蛋白VI的免疫组织化学定位

Immunohistochemical localization of collagen VI in diabetic glomeruli.

作者信息

Nerlich A G, Schleicher E D, Wiest I, Specks U, Timpl R

机构信息

Institute for Pathology, University of Munich, Germany.

出版信息

Kidney Int. 1994 Jun;45(6):1648-56. doi: 10.1038/ki.1994.216.

Abstract

Late stage diabetic nephropathy is histologically characterized by either diffuse or nodular expansion of the glomerular matrix. This is presumed to represent the morphological correlate for the functional impairment of the kidney. The exact matrix composition of the nodular glomerulosclerosis lesion of end-stage diabetic nephropathy is not known. Biochemical studies have provided evidence that the microfibrillar collagen type VI is increased in diabetic nephropathy. Consequently, this immunohistochemical study was designed to evaluate the extent and exact morphologic location of increased collagen VI deposition at various stages of diabetic glomerulosclerosis (GS). An irregular, sometimes spot-like staining of collagen VI was observed in diffuse GS in the mesangial portion. The uninterrupted staining which was evident along the glomerular basement membrane in normal glomeruli was discontinuous in diffusely sclerotic glomeruli. In nodular GS, the markedly increased deposition of collagen VI appeared to be evenly distributed throughout the entire nodular lesion. At the same time, mesangial staining for collagen IV was reduced in nodular GS, suggesting that in the expanded mesangial matrix collagen IV is progressively substituted by collagen VI during the transition from diffuse to nodular GS. The colocalization of PAS staining with collagen VI deposition in nodular GS suggests that the typical Kimmelstiel-Wilson lesions at least in part consist of collagen VI. Biochemical analysis confirmed the increased collagen VI deposition in glomeruli extracted from diabetic patients with nodular GS. Application of two antisera, recognizing primarily the alpha 1(VI)- and alpha 2(VI)-chains and the N-terminal part of alpha 3(VI)-chain, respectively, revealed no difference in staining pattern.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

晚期糖尿病肾病在组织学上的特征是肾小球基质的弥漫性或结节性扩张。这被认为是肾脏功能损害的形态学对应表现。终末期糖尿病肾病结节性肾小球硬化病变的确切基质成分尚不清楚。生化研究已提供证据表明,糖尿病肾病中微原纤维VI型胶原增加。因此,本免疫组织化学研究旨在评估糖尿病肾小球硬化(GS)各阶段胶原VI沉积增加的程度及确切形态学定位。在弥漫性GS的系膜部分观察到胶原VI呈不规则、有时为点状的染色。正常肾小球中沿肾小球基底膜明显的连续染色在弥漫性硬化的肾小球中是不连续的。在结节性GS中,胶原VI沉积明显增加,似乎均匀分布于整个结节性病变中。同时,结节性GS中IV型胶原的系膜染色减少,这表明在从弥漫性向结节性GS转变过程中,在扩张的系膜基质中IV型胶原逐渐被VI型胶原替代。结节性GS中PAS染色与胶原VI沉积的共定位表明,典型的Kimmelstiel-Wilson病变至少部分由VI型胶原组成。生化分析证实,从患有结节性GS的糖尿病患者中提取的肾小球中胶原VI沉积增加。分别应用两种主要识别α1(VI)-链和α2(VI)-链以及α3(VI)-链N端部分的抗血清,染色模式无差异。(摘要截于250字)

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