Important role for macrophages in induction of crescentic anti-GBM glomerulonephritis in WKY rats

被引:48
作者
Isome, M
Fujinaka, H
Adhikary, LP
Kovalenko, P
El-Shemi, AGA
Yoshida, Y
Yaoita, E
Takeishi, T
Takeya, M
Naito, M
Suzuki, H
Yamamoto, T
机构
[1] Niigata Univ, Grad Sch Med & Dent Sci, Inst Nephrol, Dept Struct Pathol, Niigata 9518510, Japan
[2] Niigata Univ, Grad Sch Med & Dent Sci, Dept Pathol 2, Niigata 9518510, Japan
[3] Fukushima Med Univ, Sch Med, Dept Pediat, Fukushima, Japan
[4] Niigata Natl Hosp, Dept Pediat, Kashiwazaki, Japan
[5] Kumamoto Univ, Fac Med & Pharmaceut Sci, Dept Cell Pathol, Kumamoto, Japan
关键词
anti-GBM glomerulonephritis; CD8; macrophage; monocyte; receptor; scavenger;
D O I
10.1093/ndt/gfh558
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background. A crucial role for CD8(+) cells in induction of crescentic anti-glomerular basement membrane (GBM) glomerulonephritis (GN) in WKY rats was demonstrated in studies showing that depletion of CD8(+) cells completely suppressed glomerular accumulation of monocytes/macrophages (Mo/Mphi), crescent formation and proteinuria. Because these studies did not definitively identify CD8(+) cells as the cause of tissue injury, we examined the roles of Mo/Mphi in the development of anti-GBM GN. Methods. We examined correlations between the amount of urinary protein and the numbers of glomerular CD8(+) cells or Mo/Mphi in rats after administrating different doses of anti-GBM antibody (5.0, 7.5, 10.0 and 25.0 mul/100 g body weight). The roles of Mo/Mphi in induction of GN were examined in animals by depleting Mo/Mphi in the glomerulus. To do this. rats were injected intravenously with liposome-encapsulated dichloromethylene diphosphonate (liposome-MDP) from day 3 to day 7 after anti-GBM antibody injection and they were then sacrificed at day 8. Results. Liposome-MDP treatment significantly reduced the number of ED-1(+) Mo/Mphi accumulated in glomeruli from 32.1 +/- 1.2 to 1.4 +/- 0.3/glomerular cross-section (mean +/- SD, P < 0.01), and the amount of urinary protein from 103.8 +/- 19.8 to 31.8 +/- 15.9 mg/day (P < 0.01), as well as the incidence of crescentic glomeruli from 91.3 +/- 2.7 to 23.3 +/- 7.6% (P < 0.01) at day 8. This treatment also reduced the number of CD8(+) cells accumulating in the glomeruli from 5.4 +/- 0.7 to 0.5 +/- 0.1/glomerular cross-section (P < 0.01). Upregulation of glomerular intercellular adhesion molecule 1 (ICAM-1) and monocyte chemoattractant protein 1 (MCP-1) mRNA expression was suppressed by Mo/Mphi depletion. Conclusion. These results indicate that Mo/Mphi play an important role in the induction of crescentic anti-GBM GN and glomerular injury.
引用
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页码:2997 / 3004
页数:8
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