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Yes 相关蛋白敲低通过 Erk 和 Bcl-2 信号通路的串扰诱导人牙周膜干细胞凋亡并抑制其增殖。

Knockdown of Yes-Associated Protein Induces the Apoptosis While Inhibits the Proliferation of Human Periodontal Ligament Stem Cells through Crosstalk between Erk and Bcl-2 Signaling Pathways.

机构信息

School of Stomatology, Shandong University, Jinan, China.

Shandong provincial key laboratory of oral tissue regeneration , Jinan, China.

出版信息

Int J Med Sci. 2017 Sep 19;14(12):1231-1240. doi: 10.7150/ijms.20504. eCollection 2017.

Abstract

The purpose of this study was to provide an insight into the biological effects of knockdown Yes-associated protein (YAP) on the proliferation and apoptosis of human periodontal ligament stem cells (h-PDLSCs). Immunofluorescence and Western blot were used to evaluate Hippo-YAP signaling expression level. Enhanced green fluorescence protein lentiviral vector was constructed to down-regulate YAP in h-PDLSCs. Real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR) and Western blot were used to detect the interfering efficiency of YAP expression. The proliferation activity was detected by EdU staining. Analysis of apoptosis in h-PDLSCs was done through Annexin V-APC staining, while cell cycle analysis was detected by flow cytometry. Cellular senescence was analyzed by β-galactosidase activity detection. The expression of elements in signaling pathways related with proliferation and apoptosis was detected by Western blot. YAP was located in nucleus and cytoplasm. After the lentivirus transfection, the expression of YAP mRNA and protein was significantly reduced (P<0.001). When YAP was knocked down, the proliferation activity of h-PDLSCs was inhibited; the early & late apoptosis rates increased; the proportion of cells in G1 phases increased (P<0.05), while that in G2 and S phase decreased (P<0.05); cellular senescence was accelerated (P<0.01); ERK and its target proteins P-P90RSK and P-MEK were reduced while Bcl-2 family members increased. Knockdown of YAP inhibits the proliferation activity and induces apoptosis of h-PDLSCs with the involvement of Hippo pathway and has a crosstalk between Erk and Bcl-2 signaling pathways.

摘要

本研究旨在深入了解敲低 Yes 相关蛋白(YAP)对人牙周膜干细胞(h-PDLSCs)增殖和凋亡的生物学影响。采用免疫荧光和 Western blot 评估 Hippo-YAP 信号表达水平。构建增强型绿色荧光蛋白慢病毒载体以下调 h-PDLSCs 中的 YAP。实时定量逆转录聚合酶链反应(qRT-PCR)和 Western blot 用于检测 YAP 表达的干扰效率。通过 EdU 染色检测增殖活性。通过 Annexin V-APC 染色分析 h-PDLSCs 的凋亡,通过流式细胞术检测细胞周期分析。通过β-半乳糖苷酶活性检测分析细胞衰老。通过 Western blot 检测与增殖和凋亡相关的信号通路中元素的表达。YAP 位于细胞核和细胞质中。转染慢病毒后,YAP mRNA 和蛋白的表达明显降低(P<0.001)。当 YAP 被敲低时,h-PDLSCs 的增殖活性受到抑制;早期和晚期凋亡率增加;G1 期细胞比例增加(P<0.05),而 G2 和 S 期细胞比例减少(P<0.05);细胞衰老加速(P<0.01);ERK 及其靶蛋白 P-P90RSK 和 P-MEK 减少,而 Bcl-2 家族成员增加。敲低 YAP 抑制 h-PDLSCs 的增殖活性并诱导其凋亡,涉及 Hippo 通路,并且 Erk 和 Bcl-2 信号通路之间存在串扰。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abcc/5666556/c5622dcb7560/ijmsv14p1231g001.jpg

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