Publication: Enhanced Rb/E2F and TSC/mTOR Pathways Induce Synergistic Inhibition in PDGF-Induced Proliferation in Vascular Smooth Muscle Cells
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Date
2017
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Public Library of Science
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Citation
Li, Yue, Xuan Li, Jie Liu, Wei Guo, Hongchao Zhang, and Jianchang Wang. 2017. “Enhanced Rb/E2F and TSC/mTOR Pathways Induce Synergistic Inhibition in PDGF-Induced Proliferation in Vascular Smooth Muscle Cells.” PLoS ONE 12 (1): e0170036. doi:10.1371/journal.pone.0170036. http://dx.doi.org/10.1371/journal.pone.0170036.
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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.
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Keywords
Biology and Life Sciences, Cell Biology, Cell Processes, Cell Proliferation, Oxidative Stress, Bioassays and physiological analysis, Biochemical analysis, Colorimetric assays, MTT assay, Enzyme assays, Cell Cycle and Cell Division, Genetics, Gene Expression, Biochemistry, Enzymology, Enzymes, Oxidoreductases, Luciferase, Proteins, Cell Growth, Biotechnology, Bioengineering, Synthetic Bioengineering, Genome Engineering, Synthetic Genome Editing, Crispr, Engineering and Technology, Synthetic Biology, Synthetic Genomics
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