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KMID : 0311120080490040592
Yonsei Medical Journal
2008 Volume.49 No. 4 p.592 ~ p.600
The Inhibition of Insulin-stimulated Proliferation of Vascular Smooth Muscle Cells by Rosiglitazone Is Mediated by the Akt-mTOR-P70S6K Pathway
Park Sung-Ha

Chung Nam-Sik
Cho Seung-Yun
Jang Yang-Soo
Song Hee-sang
Park Sung-ha
Lim So-yeon
Lee Sun-ju
Song Byeong-Wook
Kim Hye-Jung
Cha Min-Ji
Choi Eun-ju
Hwang Ki-Chul
Abstract
Purpose: Thiazolidinediones (TZDs) are known to inhibit the proliferation of vascular smooth muscle cell (VSMC) by increasing the activity of p27Kip1 and retinoblastoma protein (RB). However, the upstream signaling mechanisms associated with this pathway have not been elucidated. The Akt-mTOR-P70S6 kinase pathway is the central regulator of cell growth and proliferation, and increases cell proliferation by inhibiting the activities of p27Kip1 and retinoblastoma protein (RB). Therefore, we hypothesized in this study that rosiglitazone inhibits VSMC proliferation through the inhibition of the Akt-TOR-P70S6K signaling pathway.

Materials and Methods: Rat aortic smooth muscle cells (RAoSMCs) were treated with 10¥ìM of rosiglitazone 24 hours before the addition of insulin as a mitogenic stimulus. Western blot analysis was performed to determine the inhibitory effect of rosiglitazone treatment on the Akt-mTOR-P70S6K signaling pathway. Carotid balloon injury was also performed in Otsuka Long-Evans Tokushima Fatty (OLETF) diabetic rats that were pretreated with 3 mg/kg of rosiglitazone.

Results: Western blot analysis demonstrated significant inhibition of activation of p-Akt, p-m-TOR, and p-p70S6K in cells treated with rosiglitazone. The inhibition of the activation of the p-mTOR-p-p70S6K pathway seemed to be mediated by both the upstream PI3K pathway and MEK-ERK complex.

Conclusion: The inhibitory effect of rosiglitazone on RAoSMC proliferation in vitro and in vivo is mediated by the inhibition of the Akt-mTOR-P70S6K pathway.
KEYWORD
Rosiglitazone, smooth muscle cells, mammalian target of rapamycin, insulin
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