Glomerular endothelial cells respond to calcium-mobilizing agonists with release of EDRF.

Glomerular endothelial cells respond to calcium-mobilizing agonists with release of EDRF.
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肾小球内皮细胞响应钙动员激动剂并释放 EDRF。

DOI:
10.1152/ajprenal.1990.258.5.f1295
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发表时间:
1990
期刊:
The American journal of physiology
影响因子:
--
通讯作者:
Ballermann,BJ
Ballermann,BJ
中科院分区:
--
文献类型:
--
作者:
Marsden,PA;Brock,TA;Ballermann,BJ

文献摘要

被引文献

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为了确定肾小球内皮细胞(glomerular endothelial cells, GEN)是否通过释放内皮源性松弛因子(endothelial -derived relax factor, EDRF)在局部控制肾小球功能中发挥作用,我们测定了几种激动剂对GEN胞质钙浓度([Ca2+]i)和GEN EDRF释放的影响。缓激素、ATP、凝血酶和血小板活化因子(PAF)均以浓度依赖性的方式增加GEN中的[Ca2+]i,而血清素、乙酰胆碱、苯肾上腺素和内皮素-1则没有影响。将肾小球系膜细胞(GMC)与GEN增强的系膜细胞鸟苷3′,5′-环单磷酸(cGMP)含量共孵育5 - 6倍,缓激肽引起GMC cGMP含量在GEN存在而不是不存在的情况下进一步呈浓度依赖性增加。GEN依赖的缓激肽刺激的GMC cGMP积累被血红蛋白和亚甲基蓝所消除,被棉酚所钝化,并被超氧化物歧化酶所增强。其他能够增加GEN [Ca2+]i的激动剂也能在GEN存在而不存在的情况下刺激GMC cGMP的积累,因此培养的GEN释放一种刺激邻近系膜细胞cGMP积累的因子,具有EDRF的药理学特征。
To determine whether glomerular endothelial cells (GEN) may play a role in the local control of glomerular function by releasing endothelium-derived relaxing factor (EDRF), the effect of several agonists on GEN cytosolic calcium concentration ([Ca2+]i) and GEN EDRF release was determined. Bradykinin, ATP, thrombin, and platelet-activating factor (PAF) all increased [Ca2+]i in GEN in a concentration-dependent manner, whereas serotonin, acetylcholine, phenylephrine, and endothelin-1 were without effect. Coincubation of glomerular mesangial cells (GMC) with GEN augmented mesangial cell guanosine 3',5'-cyclic monophosphate (cGMP) content five- to sixfold, Bradykinin elicited a further concentration-dependent increase in GMC cGMP content in the presence but not absence of GEN. The GEN-dependent bradykinin-stimulated GMC cGMP accumulation was abolished by hemoglobin and methylene blue, blunted by gossypol, and augmented by superoxide dismutase. Other agonists capable of augmenting GEN [Ca2+]i also stimulated GMC cGMP accumulation in the presence but not in the absence of GEN. Thus cultured GEN release a factor that stimulates cGMP accumulation in adjacent mesangial cells which has the pharmacological characteristics of EDRF.