Interleukin-4 modulates collagen synthesis by human mesangial cells in a type-specific manner

被引:15
作者
Nakazato, Y
Okada, H
Tajima, S
Hayashida, T
Kanno, Y
Suzuki, H
Saruta, T
机构
[1] KEIO UNIV, SCH MED, DEPT INTERNAL MED, SHINJUKU KU, TOKYO 160, JAPAN
[2] KEIO UNIV, SCH MED, DEPT DERMATOL, HLTH CTR, SHINJUKU KU, TOKYO 160, JAPAN
来源
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY | 1996年 / 270卷 / 03期
关键词
interleukin-1; type III collagen; western blot; glomerulonephritis;
D O I
10.1152/ajprenal.1996.270.3.F447
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Several studies have suggested an involvement of interleukin (IL)-4 in the pathophysiology of glomerulonephritis (GN). To elucidate its possible role in GN, we have investigated the effect of IL-4 on collagen accumulation by human mesangial cells (MC). After incubation with IL-1 alpha and/or IL-4 for 48 h, types I, III, and IV collagen in both soluble and cell-associated forms were identified by Western blotting. IL-1 alpha stimulated type I and IV collagen synthesis, lacking significant effect on type III collagen synthesis. In contrast, IL-4 stimulated type III collagen synthesis without affecting type I and type TV synthesis. Enzyme-linked immunosorbent assay confirmed the dose-dependent effect of IL-4 on collagen type III secretion (2.0-fold at 10 ng/ml). Importantly, IL-1 alpha-stimulated type I and IV collagen synthesis was suppressed by concomitant IL-4 treatment. Northern analysis of type I and III procollagen mRNAs displayed consistent results. These data indicate that IL-4 selectively stimulates type III collagen synthesis but also suppresses IL-1 alpha-stimulated type I and IV collagen synthesis. Therefore IL-4 could potentially contribute to the pathological changes in glomerular diseases in cooperate with other cytokines.
引用
收藏
页码:F447 / F453
页数:7
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