Marsden P A, Dorfman D M, Collins T, Brenner B M, Orkin S H, Ballermann B J
Harvard Center for the Study of Kidney Diseases, Brigham and Women's Hospital, Boston, Massachusetts.
Am J Physiol. 1991 Jul;261(1 Pt 2):F117-25. doi: 10.1152/ajprenal.1991.261.1.F117.
Endothelin (ET)-1 is a powerful vasoconstrictor known to be produced and secreted by endothelial cells lining large vessels. Because ET-1 stimulates glomerular mesangial cell contraction, glomerular capillary endothelial cells (GEN), normally situated in close apposition to mesangial cells, were examined for potential ET expression and secretion. Cultured bovine GEN released ET in a time-dependent fashion. ET secretion was significantly stimulated by bradykinin, an agonist known to activate phospholipase C in these cells. Preproendothelin 1 (preproET-1) mRNA levels in GEN rose in a biphasic manner on stimulation with bradykinin. The early increments (at 30 min) were not dependent on new protein synthesis, whereas the late rise (6 h after addition of bradykinin) appeared to be protein synthesis dependent. Neither early or late bradykinin-stimulated preproET-1 mRNA expression in glomerular endothelial cells was due to inhibition of mRNA breakdown. Both phases of preproET-1 mRNA expression were observed with other glomerular endothelial cell calcium-mobilizing agonists, namely thrombin, and were mimicked by the calcium ionophore ionomycin. By contrast, the protein kinase C activator phorbol myristate acetate only enhanced preproET-1 mRNA expression at 30 min and suppressed expression thereafter. It is concluded that GEN have the potential to express and secrete ET-1 in a phospholipase C-regulated fashion. Furthermore, because glomerular mesangial cells respond to this peptide, the findings raise the possibility of paracrine regulation of mesangial cell tone by glomerular endothelial cell-derived ET-1.
内皮素(ET)-1是一种强效血管收缩剂,已知由大血管内衬的内皮细胞产生和分泌。由于ET-1刺激肾小球系膜细胞收缩,因此对通常与系膜细胞紧密相邻的肾小球毛细血管内皮细胞(GEN)进行了潜在ET表达和分泌的检测。培养的牛GEN以时间依赖性方式释放ET。缓激肽是一种已知能激活这些细胞中磷脂酶C的激动剂,可显著刺激ET分泌。用缓激肽刺激后,GEN中前内皮素原1(preproET-1)mRNA水平呈双相上升。早期增加(30分钟时)不依赖于新的蛋白质合成,而后期上升(添加缓激肽后6小时)似乎依赖于蛋白质合成。肾小球内皮细胞中缓激肽刺激的preproET-1 mRNA表达的早期或晚期阶段均不是由于mRNA降解受到抑制所致。用其他肾小球内皮细胞钙动员激动剂(即凝血酶)也观察到了preproET-1 mRNA表达的两个阶段,并且钙离子载体离子霉素可模拟这种表达。相比之下,蛋白激酶C激活剂佛波醇肉豆蔻酸酯仅在30分钟时增强preproET-1 mRNA表达,此后则抑制表达。得出的结论是,GEN有潜力以磷脂酶C调节的方式表达和分泌ET-1。此外,由于肾小球系膜细胞对这种肽有反应,这些发现增加了肾小球内皮细胞衍生的ET-1对系膜细胞张力进行旁分泌调节的可能性。