胰岛素影响自发性高血压大鼠血管平滑肌细胞增殖及肌动蛋白分布的丝裂原激酶的机制探讨

Effects of insulin on the distribution of actins in vascular smooth muscle cells in the process of proliferation via mitogen-activated protein kinase in vitro

血管平滑肌细胞增殖的同时伴有细胞内肌动蛋白分布的改变 ,这种改变受PKC MAPK信号转导途径调控 ,但目前机制尚不清楚。为探讨胰岛素对PKC MAPK信号转导途径参与调控血管平滑肌细胞增殖及细胞内肌动蛋白分布的影响 ,本研究用PKC抑制剂预处理SHR大鼠体外培养的血管平滑肌细胞 ,观察预处理的血管平滑肌细胞经胰岛素刺激后细胞内DNA的合成、MAPK的活性、表达及细胞内肌动蛋白的分布。发现 ,胰岛素刺激后可使血管平滑肌细胞增殖 ,同时伴有 [3 H]TdR掺入增加、MAPK活性及表达与对照组比较明显升高。这些作用可被PKC抑制剂阻断。胰岛素在刺激血管平滑肌细胞增殖的同时也使细胞内肌动蛋白重新分布 ,这一效应也可被PKC抑制剂阻断。上述结果提示 。

Proliferation of vascular smooth muscle cells (VSMCs) is often accompanied by changes in intracellular actin distribution The changes are controlled by the signal transduction pathways of protein kinase C/mitogenic activated protein kinase (PKC MAPK), but the mechanism is unclear In order to study the effect of insulin on the intracellular signal transduction (PKC MAPK) probably involved in the modulation of proliferation and redistribution of actins in the VSMCs, the DNA synthesis, MAPK activities and its gene expression, and the redistribution of intracellular actins were investigated in the isolated VSMCs of SHR pretreated with PKC inhibitor and/or insulin, respectively We found that insulin treatment resulted in a proliferation of the VSMCs and an increase in TdR incorpovation. Meanwhile, the activities and expression of MAPK increased significantly compared to the control group. These effects of insulin were blocked by PKC inhibitor. In addition, insulin caused a redistribution of the intracellular actins in VSMCs, which was also inhibited by PKC inhibitor. It is, therefore, suggested that these effects of insulin on VSMCs proliferation and distribution of the intracellular actins may be mediated by the MAPK signal transduction pathway.