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.
- Author:
Xu-Kai WANG
1
;
Yan WANG
;
Zuo-Yun HE
;
Guang-Yao LIU
;
Cheng-Ming YANG
Author Information
1. Department of Cardiology, Daping Hospital, The 3rd Military Medical University, Chongqing 400042. wangxuk@btamail.net.cn
- Publication Type:Journal Article
- MeSH:
Actins;
metabolism;
Animals;
Cell Division;
drug effects;
In Vitro Techniques;
Insulin;
pharmacology;
Mitogen-Activated Protein Kinases;
physiology;
Muscle, Smooth, Vascular;
cytology;
Myocytes, Smooth Muscle;
drug effects;
enzymology;
metabolism;
Protein Kinase C;
physiology;
Rats;
Rats, Inbred SHR;
Tissue Distribution
- From:
Acta Physiologica Sinica
2002;54(2):165-170
- CountryChina
- Language:Chinese
-
Abstract:
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 proliferation of the VSMCs and an increase in [(3)H] TdR incorporation. 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.
