RRC ID 12042
Author Nakano N, Urasawa K, Takagi Y, Saito T, Kaneta S, Ishikawa S, Higashi H, Tsutsui H, Hatakeyama M, Kitabatake A.
Title Downregulation of cyclin-dependent kinase inhibitor; p57(kip2), is involved in the cell cycle progression of vascular smooth muscle cells.
Journal Biochem. Biophys. Res. Commun.
Abstract Immature vascular smooth muscle cells (VSMCs) proliferate responding to extrinsic mitogens and accumulate in neointima after arterial injuries. Cell proliferation is positively regulated by cyclin/cyclin-dependent kinase (CDK) complex and negatively controlled by CDK inhibitors; CKIs such as p27(kip1) and p57(kip2). In this study, embryonic rat thoracic aorta VSMCs; A10 were G0/G1 arrested by serum starvation, re-stimulated with serum, and harvested every four hours. Both CKIs co-expressed in quiescent VSMCs and rapidly diminished by stimulation. Protein level of p27(kip1) was regulated by both transcription and post-transcription, but that of p57(kip2) was mainly by post-transcription. Supplemental overexpression of p57(kip2) inhibited the activations of G1 cyclin/CDKs and subsequent hyperphosphorylations of all three retinoblastoma pocket proteins as well as G1/S transition of cell cycle. Our findings suggest that the downregulations of not only p27(kip1), but also p57(kip2) responding to mitogenic stimulation, play key roles in the cell cycle progression of VSMCs.
Volume 338(3)
Pages 1661-7
Published 2005-12-23
DOI 10.1016/j.bbrc.2005.10.093
PII S0006-291X(05)02344-2
PMID 16259944
MeSH Animals Cell Cycle / physiology* Cells, Cultured Cyclin G Cyclin G1 Cyclin-Dependent Kinase Inhibitor p57 / genetics Cyclin-Dependent Kinase Inhibitor p57 / metabolism* Cyclins / metabolism Down-Regulation* Gene Expression Regulation, Enzymologic Muscle, Smooth, Vascular / cytology* Muscle, Smooth, Vascular / metabolism* Protein Binding RNA, Messenger / genetics Rats Serum
IF 2.559
Times Cited 9
WOS Category BIOPHYSICS BIOCHEMISTRY & MOLECULAR BIOLOGY
Resource
DNA material pAxCAwt pAdex1CAwt (RDB1678)