PARTICLES FROM DIALYSIS TUBING STIMULATE INTERLEUKIN-1 SECRETION BY MACROPHAGES

被引:14
|
作者
BOMMER, J
WEINREICH, T
LOVETT, DH
BOUILLON, R
RITZ, E
GEMSA, D
机构
[1] VET ADM MED CTR, UNIV CALIF, SAN FRANCISCO, CA 94121 USA
[2] CATHOLIC UNIV LEUVEN, DEPT ENDOCRINOL, B-3000 LOUVAIN, BELGIUM
[3] UNIV MARBURG, INST IMMUNOL, W-3550 MARBURG, GERMANY
关键词
Bioincompatibility; Haemodialysis; Interleukin; 1; Macrophages; Uraemia;
D O I
10.1093/ndt/5.3.208
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
Loading of tissue macrophages with dialysistubing-derived particles may occur during chronic haemodialysis. Previous studies have demonstrated that these particle-laden macrophages release significant quantities of prostaglandins. In these experiments, the effects of dialysis-tubing-particle loading on the release of the central inflammatory mediator, interleukin 1 (IL 1), was examined. Rats received daily injections of silicone or polyvinylchloride (PVC) particles, and were compared to animals given saline alone. The silicone and PVC groups received a total of 3 A-109 particles over a 4-week period. Non-stimulated peritoneal macrophages from control animals released a median of 4.1 (range 1.2-10.3) U IL 1 per 106 cells. In contrast, macrophages from silicone- and PVC-loaded animals spontaneously released high levels of IL 1 (median 21.8; range 10-36.7) and 94 (range 36-336) U per 106 cells respectively). Following in vitro stimulation with bacterial iipopolysaccharide (LPS), peritoneal macrophages from silicone- and PVC-treated animals released large amounts of IL 1 (median 538 (range 359-2017) U and median 653 (range 326-1134) U per 106 cells, respectively) as compared to LPS-stimulated macrophages from control animals (median 332 (range 130-306) U per 106 cells)). Zymosan or LPS stimulation of splenic cells from silicone- and PVC-loaded animals also secreted increased quantities of IL 1 as compared to controls. The chronic loading of tissue macrophages in dialysis patients with tubing-derived particles may result in augmented release of IL 1, with subsequent activation of inflammatory processes. © 1990 European Dialysis and Transplant Association-European Renal Association.
引用
收藏
页码:208 / 213
页数:6
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