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增强的Rb/E2F和TSC/mTOR信号通路协同抑制血小板衍生生长因子诱导的血管平滑肌细胞增殖。

Enhanced Rb/E2F and TSC/mTOR Pathways Induce Synergistic Inhibition in PDGF-Induced Proliferation in Vascular Smooth Muscle Cells.

作者信息

Li Yue, Li Xuan, Liu Jie, Guo Wei, Zhang Hongchao, Wang Jianchang

机构信息

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.

出版信息

PLoS One. 2017 Jan 11;12(1):e0170036. doi: 10.1371/journal.pone.0170036. eCollection 2017.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba04/5226788/2fcabd93ce8b/pone.0170036.g001.jpg

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