Sawada T, Haneda M, Togawa M, Kikkawa R
Third Department of Medicine, Shiga University of Medical Science, Japan.
Nihon Jinzo Gakkai Shi. 1996 Nov;38(11):469-74.
Mesangial expansion is one of the histological abnormalities observed among the various glomerular diseases. It is due largely to the accumulation of extracellular matrix (ECM) proteins, such as type IV collagen, laminin and fibronectin. In order to examine the abilities of mesangial cells to produce type IV collagen, we used enzyme-linked immunosorbent assay to measure type IV collagen secreted from cultured rat mesangial cells. After exposing confluent cells to endothelin-1 (ET-1, 0.01 microM), insulin-like growth factor-1 (100 ng/ml) angiotensin-II (1 microM) and transforming growth factor-beta (1 ng/ml) for 24 hours, type IV collagen production increased 1.5 approximately 2.5 times. ET-1 stimulated type IV collagen production in a dose-dependent fashion, and this effect was blocked by the protein kinase C inhibitor, staurosporine. Atrial natriuretic peptide (ANP) inhibited the increase in type IV collagen production caused by ET-1 in a dose-dependent fashion. Addition of 8-bromo-cGMP similarly suppressed the stimulation of type IV collagen production caused by ET-1. These findings indicate that ET-1 stimulates type IV collagen synthesis in cultured rat mesangial cells by a mechanism probably involving activation of PKC, and that ANP inhibits ET-1-induced production of type IV collagen through a cGMP-dependent process.
系膜扩张是各种肾小球疾病中观察到的组织学异常之一。这主要归因于细胞外基质(ECM)蛋白的积累,如IV型胶原、层粘连蛋白和纤连蛋白。为了检测系膜细胞产生IV型胶原的能力,我们使用酶联免疫吸附测定法来测量培养的大鼠系膜细胞分泌的IV型胶原。将汇合的细胞暴露于内皮素-1(ET-1,0.01微摩尔)、胰岛素样生长因子-1(100纳克/毫升)、血管紧张素-II(1微摩尔)和转化生长因子-β(1纳克/毫升)24小时后,IV型胶原的产生增加了1.5至2.5倍。ET-1以剂量依赖的方式刺激IV型胶原的产生,并且这种效应被蛋白激酶C抑制剂星形孢菌素阻断。心房利钠肽(ANP)以剂量依赖的方式抑制ET-1引起的IV型胶原产生的增加。添加8-溴-cGMP同样抑制了ET-1对IV型胶原产生的刺激。这些发现表明,ET-1通过一种可能涉及蛋白激酶C激活的机制刺激培养的大鼠系膜细胞中IV型胶原的合成,并且ANP通过一个cGMP依赖的过程抑制ET-1诱导的IV型胶原的产生。