Adoptive transfer of genetically modified macrophages elucidated TGF-β-mediated 'self-defence' of the glomerulus against local action of macrophages

被引:6
作者
Kitamura, M [1 ]
机构
[1] UCL, Sch Med, Rayne Inst, Dept Med Glomerular Bioengn Unit, London WC1E 6JJ, England
关键词
D O I
10.1093/ndt/14.suppl_1.35
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
TGF-beta has several anti-inflammatory properties which may be relevant to prevention of or recovery from acute glomerular inflammation. Using genetically modified mesangial cells and a technique for in vivo macrophage transfer, this article provides evidence for TGF-beta-mediated 'self-defence' of the glomerulus against macrophages. Rat mesangial cells stably transfected with TGF-beta 1 showed a blunted response to the macrophage-derived, proinflammatory cytokine IL-1 beta. In contrast, mesangial cells expressing the dominant-interfering TGF-beta receptor showed an enhanced response to IL-1. Similarly, externally added TGF-beta 1 inhibited the cytokine response of normal glomeruli, and isolated nephritic glomeruli producing active TGF-beta 1 showed a depressed response to IL-1 beta, compared to normal glomeruli. Consistent with these in vitro results, in vivo transfer of activated macrophages revealed that the TGF-beta-producing glomeruli are insensitive to the effector action of macrophages. These results indicate that TGF-beta 1 functions as an endogen ous 'defender' that counteracts local action of activated macrophages in the glomerulus.
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页码:35 / 38
页数:4
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