ATRIAL-NATRIURETIC-FACTOR MODULATES NITRIC-OXIDE PRODUCTION - AN ANF-C RECEPTOR-MEDIATED EFFECT

被引:41
作者
MCLAY, JS [1 ]
CHATTERJEE, PK [1 ]
JARDINE, AG [1 ]
HAWKSWORTH, GM [1 ]
机构
[1] UNIV GLASGOW,WESTERN INFIRM,DEPT MED & THERAPEUT,GLASGOW G11 6NT,LANARK,SCOTLAND
关键词
ANF; ANF-C RECEPTOR; NITRIC OXIDE; IMMUNOMODULATION; CYCLIC GMP; CYTOKINE;
D O I
10.1097/00004872-199506000-00008
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Objectives: To investigate the possible immunomodulatory and regulatory functions of atrial natriuretic factor (ANF) and the natriuretic peptide C (NPR-C) receptor in the control of cytokine-stimulated nitric oxide production in primary cultures of human proximal tubular cells. Methods: Freshly prepared human proximal tubular cells were seeded on plastic plates and allowed to reach confluence. The confluent cells were then incubated with ANF or cyclic((4-23))ANF (C-(4-23)ANF) alone, or preincubated with ANF or C-(4-23)ANF before incubation with the nitric oxide-stimulating combination of cytokines interleukin-1 beta (10 u/ml), tumour necrosis factor-alpha (10 ng/ml) and interferon-gamma (100 u/ml). Results: In the present series of experiments we have found that incubation of primary cultures of human proximal tubular cells with ANF or C-(4-23)ANF stimulates nitric oxide production dose-dependently, Paradoxically, ANF acting via the NPR-C receptor also inhibits cytokine activation of the enzyme-inducible nitric oxide synthase via a cyclic GMP-independent mechanism. Both of these effects were reproduced by the NPR-C receptor-specific ligand C-(4-23)ANF. Conclusions: These findings represent novel actions of ANF mediated via the NPR-C receptor. The results also provide a simple model system in which to study the subcellular mechanisms of NPR-C receptor activation.
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页码:625 / 630
页数:6
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