Ribozyme targeting of receptor for advanced glycation end products in mouse mesangial cells

被引:49
作者
Tsuji, H [1 ]
Iehara, N
Masegi, T
Imura, M
Ohkawa, J
Arai, H
Ishii, K
Kita, T
Doi, T
机构
[1] Kyoto Univ, Fac Med, Dept Geriatr Med, Sakyo Ku, Kyoto 606, Japan
[2] Kyoto Univ, Fac Med, Div Artificial Kidneys, Sakyo Ku, Kyoto 606, Japan
[3] Univ Tsukuba, Inst Appl Biochem, Tsukuba, Ibaraki 305, Japan
基金
日本学术振兴会;
关键词
D O I
10.1006/bbrc.1998.8489
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Accumulation of extracellular matrix is a characteristic of diabetic nephropathy, and advanced glycation end products (AGEs) are considered to play an important role in the mechanism. To investigate the involvement of the receptor for AGE (RAGE) in upregulation of type IV collagen by AGES, we applied the hammerhead ribozyme for targeting RAGE. We established a stable mouse mesangial cell line that produces the RAGE-specific ribozyme (Rz-RAGE). Both the RAGE mRNA and protein were decreased in the cell line. The amount of type IV collagen mRNA increased by AGES' treatment in control cells. In contrast, the increase of type IV collagen induced by AGEs was not observed in the Rz-RAGE-producing cells. We conclude that the induction of type IV collagen by AGEs is mediated by RAGE and this mechanism could be involved in diabetic nephropathy. This study also suggested the experimental/therapeutic potential of hammerhead ribozymes. (C) 1998 Academic Press.
引用
收藏
页码:583 / 588
页数:6
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