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VIII型胶原蛋白在人类糖尿病肾病中的表达

Collagen type VIII expression in human diabetic nephropathy.

作者信息

Gerth J, Cohen C D, Hopfer U, Lindenmeyer M T, Sommer M, Gröne H J, Wolf G

机构信息

University of Jena, Jena, Germany.

出版信息

Eur J Clin Invest. 2007 Oct;37(10):767-73. doi: 10.1111/j.1365-2362.2007.01864.x.

Abstract

BACKGROUND

Collagen type VIII is a non-fibrillar short-chain collagen that may modulate migration, proliferation and adherence of various cells. Only very sparse information exists on collagen type VIII expression in human diabetic nephropathy.

MATERIAL AND METHODS

We retrospectively studied mRNA expression for the two collagen type VIII chains (COL8A1 and COL8A2) in 20 biopsies with histologically confirmed diabetic nephropathy by real-time PCR, and compared glomerular and tubular expression with normal kidney [pre-transplant biopsies (n = 10)]. Expression of collagen type VIII was also studied in biopsies from patients with benign nephrosclerosis (BNS; n = 16) and focal-segmental glomerulosclerosis (FSGS; n = 9).

RESULTS

A strong specific induction of COL8A1 mRNA was found in diabetic nephropathy in both glomerular and tubular compartments. There was also a robust induction of COL8A2 in diabetic nephropathy, but overall expression was lower than that of COL8A1 transcripts. No significant increase in COL8A1 and COL8A2 mRNAs expression was found in biopsies from patients with BNS and FSGS compared with normal kidneys. The cross-reactivity of the used anti-alpha1(VIII) antibody with human tissue was confirmed by Western blots. Immunohistological analysis revealed only little staining for collagen type VIII in the normal kidney, localized to vessels. There was an up-regulation of collagen type VIII protein expression as shown by immunohistochemistry in the diabetic nephropathy biopsies mainly localized to mesangial cells, tubules and the interstitium. Proteinuria and serum creatinine did not correlate with glomerular or tubular COL8A1 and COL8A2 mRNA expression in diabetic patients.

CONCLUSION

Our study systemically investigates collagen type VIII expression in human biopsies. Induction of collagen type VIII was specific for diabetic nephropathy and did not occur in the other renal diseases studied. More specific factors of the diabetic environment are likely involved in the stimulated expression because there was no correlation of collagen type VIII mRNA expression with proteinuria. Since collagen type VIII may influence proliferation and migration of cells, it is possible that an increase in renal expression of collagen type VIII initiates other pathophysiological processes (e.g. proliferation of renal fibroblasts) involved in diabetic nephropathy.

摘要

背景

VIII型胶原蛋白是一种非纤维状短链胶原蛋白,可能调节多种细胞的迁移、增殖和黏附。关于VIII型胶原蛋白在人类糖尿病肾病中的表达,仅有非常稀少的信息。

材料与方法

我们通过实时PCR回顾性研究了20例经组织学确诊为糖尿病肾病的活检组织中两条VIII型胶原链(COL8A1和COL8A2)的mRNA表达,并将肾小球和肾小管的表达与正常肾脏[移植前活检组织(n = 10)]进行比较。还研究了良性肾硬化(BNS;n = 16)和局灶节段性肾小球硬化(FSGS;n = 9)患者活检组织中VIII型胶原蛋白的表达。

结果

在糖尿病肾病的肾小球和肾小管区域均发现COL8A1 mRNA有强烈的特异性诱导。糖尿病肾病中COL8A2也有明显诱导,但总体表达低于COL8A1转录本。与正常肾脏相比,BNS和FSGS患者活检组织中COL8A1和COL8A2 mRNA表达无显著增加。Western印迹证实了所用抗α1(VIII)抗体与人体组织的交叉反应性。免疫组织学分析显示,正常肾脏中VIII型胶原蛋白染色极少,局限于血管。免疫组织化学显示,糖尿病肾病活检组织中VIII型胶原蛋白蛋白表达上调,主要定位于系膜细胞、肾小管和间质。糖尿病患者的蛋白尿和血清肌酐与肾小球或肾小管COL8A1和COL8A2 mRNA表达无相关性。

结论

我们的研究系统地调查了人类活检组织中VIII型胶原蛋白的表达。VIII型胶原蛋白的诱导是糖尿病肾病特有的,在其他所研究的肾脏疾病中未发生。由于VIII型胶原蛋白mRNA表达与蛋白尿无相关性,糖尿病环境中更特异的因素可能参与了其表达的刺激。由于VIII型胶原蛋白可能影响细胞的增殖和迁移,肾脏中VIII型胶原蛋白表达的增加可能引发糖尿病肾病中其他病理生理过程(如肾成纤维细胞增殖)。

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