Immunohistochemical characterization of glomerular PDGF B-chain and PDGF β-receptor expression in diabetic rats

被引:89
作者
Nakagawa, H
Sasahara, M
Haneda, M [1 ]
Koya, D
Hazama, F
Kikkawa, R
机构
[1] Shiga Univ Med Sci, Dept Med 3, Otsu, Shiga 5202192, Japan
[2] Shiga Univ Med Sci, Dept Lab Med, Otsu, Shiga 5202192, Japan
[3] Shiga Univ Med Sci, Dept Pathol 2, Otsu, Shiga 5202192, Japan
关键词
platelet-derived growth factor; diabetic nephropathy; immunohistochemistry; mesangial cells; visceral epithelial cells;
D O I
10.1016/S0168-8227(99)00144-8
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Platelet-derived growth factor (PDGF) was found to contribute to the pathophysiological process in the development and progression of glomerulosclerosis characterized by mesangial cell proliferation and accumulation of extracellular matrix. To examine the role of PDGF in the development of diabetic nephropathy, we conducted immunohistochemical analysis for PDGF B-chain (PDGF-B) and PDGF beta-receptor (PDGFR-beta) in the glomeruli of streptozotocin-induced diabetic rats. At 2, 4, and 12 weeks after the onset of diabetes, the expression of PDGF-B ill glomeruli of diabetic rats was increased significantly as compared to control or diabetic rats treated with insulin. Similar changes were observed on PDGFR-beta immunostaining. The immunostaining of mirror sections revealed the existence of PDGF-B or PDGFR-beta not only in mesangial cells but also in visceral epithelial cells. Glomerular volume was significantly increased ill diabetes. This early glomerular abnormality was prevented by an inhibition of PDGF system with trapidil as well as by the treatment of insulin. Our results suggest that the activation of the PDGF system in glomerular cells might play an important role in the development of early glomerular lesion in diabetes. (C) 2000 Elsevier Science ireland Ltd. All rights reserved.
引用
收藏
页码:87 / 98
页数:12
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