首页> 美国卫生研究院文献>International Journal of Medical Sciences >Activated Yes-Associated Protein Accelerates Cell Cycle Inhibits Apoptosis and Delays Senescence in Human Periodontal Ligament Stem Cells
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Activated Yes-Associated Protein Accelerates Cell Cycle Inhibits Apoptosis and Delays Senescence in Human Periodontal Ligament Stem Cells

机译:激活的是相关蛋白加速人类牙周膜干细胞的细胞周期抑制细胞凋亡并延缓衰老。

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摘要

>Objectives: To provide insight into the biological effects of activated Yes-associated protein (YAP) on the proliferation, apoptosis, and senescence of human periodontal ligament stem cells (h-PDLSCs).>Methods: h-PDLSCs were isolated by the limiting dilution method, and their surface markers were quantified by flow cytometry. Enhanced green fluorescence protein (EGFP)-labeled lentiviral vector was used to activate YAP in h-PDLSCs, then qRT-PCR and Western blotting were used to evaluate the expression level of YAP. Immunofluorescence was used to detect the location of YAP in h-PDLSCs. The proliferation activity was detected by cell counting kit-8 (CCK-8) and 5-ethynyl-2'-deoxyuridine (EdU), and the cell cycle was determined by flow cytometry. Apoptosis was analyzed by Annexin V-APC staining. Cell senescence was detected by β-galactosidase staining. Proteins in ERK, Bcl-2, and p53 signaling pathways were detected by Western blotting.>Results: h-PDLSCs were isolated successfully and were positive for human mesenchymal stem cell surface markers. After YAP was activated by lentiviral vector, the mRNA and protein of YAP were highly expressed, and more YAP translocated into the nucleus. When YAP was overexpressed in h-PDLSCs, proliferation activity was improved; early and late apoptosis rates decreased (P<0.05); the proportion of cells in G2/M phases increased (P<0.05), while that in G0/G1 phase decreased (P<0.05); cellular senescence was delayed (P<0.01); the expression of P-MEK, P-ERK, P-P90RSK and P-Msk increased, while the expression of Bcl-2 family members (Bak, Bid and Bik) decreased.>Conclusions: Activated YAP promotes proliferation, inhibits apoptosis, and delays senescence of h-PDLSCs. The Hippo-YAP signaling pathway can influence ERK and Bcl-2 signaling pathways.
机译:>目的:目的是了解激活的Yes关联蛋白(YAP)对人牙周膜干细胞(h-PDLSCs)增殖,凋亡和衰老的生物学影响。>方法: 通过有限稀释法分离出h-PDLSCs,并通过流式细胞仪对其表面标志物进行定量。用增强绿色荧光蛋白(EGFP)标记的慢病毒载体激活h-PDLSCs中的YAP,然后用qRT-PCR和Western blotting评估YAP的表达水平。免疫荧光用于检测hAPDSLS中YAP的位置。通过细胞计数试剂盒8(CCK-8)和5-乙炔基-2'-脱氧尿苷(EdU)检测增殖活性,并通过流式细胞术确定细胞周期。通过膜联蛋白V-APC染色分析细胞凋亡。通过β-半乳糖苷酶染色检测细胞衰老。通过Western blotting检测ERK,Bcl-2和p53信号通路中的蛋白质。>结果: h-PDLSCs成功分离,对人间充质干细胞表面标志物呈阳性。慢病毒载体激活YAP后,YAP的mRNA和蛋白高度表达,更多的YAP易位到细胞核中。当在h-PDLSCs中过表达YAP时,增殖活性得到改善。早期和晚期细胞凋亡率降低(P <0.05); G2 / M期细胞比例增加(P <0.05),而G0 / G1期细胞减少(P <0.05);细胞衰老延迟(P <0.01); P-MEK,P-ERK,P-P90RSK和P-Msk的表达增加,而Bcl-2家族成员(Bak,Bid和Bik)的表达减少。>结论:活化的YAP促进了增殖,抑制细胞凋亡,并延迟h-PDLSCs的衰老。 Hippo-YAP信号通路可以影响ERK和Bcl-2信号通路。

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