Li Yue, Li Xuan, Liu Jie, Guo Wei, Zhang Hongchao, Wang Jianchang
Department of Cardiac surgery, Air Force General Hospital of People`s Liberation Army, Beijing, China.
Department of Vascular and Thyroid Surgery, 1st Hospital of China Medical University, Shenyang, Liaoning, China.
PLoS One. 2017 Jan 11;12(1):e0170036. doi: 10.1371/journal.pone.0170036. eCollection 2017.
Platelet-derived growth factor (PDGF) plays an essential role in proliferation of vascular smooth muscle cells (VSMCs). The Rb/E2F and TSC/mTOR pathways contribute to the proliferation of VSMCs, but its exact roles in PDGF-induced proliferation are unclear. In this study, we demonstrated the roles of Rb/E2F and TSC/mTOR pathways in PDGF-induced proliferation in VSMCs. We found that PDGF stimulates the activity of E2F and mTOR pathways, and knockdown of either Rb or TSC2 increases PDGF-induced proliferation in VSMCs. More interestingly, we revealed that enhancing both E2F and mTOR activity leads to synergistic inhibition of PDGF-induced proliferation in VSMCs. We further identified that the synergistic inhibition effect is caused by the induced oxidative stress. Summarily, these data suggest the important regulations of Rb/E2F and TSC/mTOR pathways in PDGF-induced proliferation in VSMCs, and also present a promising way to limit deregulated proliferation by PDGF induction in VSMCs.
血小板衍生生长因子(PDGF)在血管平滑肌细胞(VSMC)增殖中起重要作用。Rb/E2F和TSC/mTOR信号通路参与VSMC的增殖,但其在PDGF诱导的增殖中的具体作用尚不清楚。在本研究中,我们证明了Rb/E2F和TSC/mTOR信号通路在PDGF诱导的VSMC增殖中的作用。我们发现PDGF刺激E2F和mTOR信号通路的活性,敲低Rb或TSC2均可增加PDGF诱导的VSMC增殖。更有趣的是,我们发现增强E2F和mTOR活性会协同抑制PDGF诱导的VSMC增殖。我们进一步确定这种协同抑制作用是由诱导的氧化应激引起的。总之,这些数据表明Rb/E2F和TSC/mTOR信号通路在PDGF诱导的VSMC增殖中具有重要调节作用,也为限制PDGF诱导的VSMC增殖失控提供了一种有前景的方法。