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

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 l...

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Veröffentlicht in:International journal of medical sciences 2017-01, Vol.14 (12), p.1231-1240
Hauptverfasser: Wen, Yong, Ji, Yawen, Zhang, Yunpeng, Jiang, Baoqi, Tang, Cuizhu, Wang, Qi, Chen, Xiyan, Jia, Linglu, Gu, Weiting, Xu, Xin
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container_issue 12
container_start_page 1231
container_title International journal of medical sciences
container_volume 14
creator Wen, Yong
Ji, Yawen
Zhang, Yunpeng
Jiang, Baoqi
Tang, Cuizhu
Wang, Qi
Chen, Xiyan
Jia, Linglu
Gu, Weiting
Xu, Xin
description 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
doi_str_mv 10.7150/ijms.20504
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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&lt;0.001). When YAP was knocked down, the proliferation activity of h-PDLSCs was inhibited; the early &amp; late apoptosis rates increased; the proportion of cells in G1 phases increased (P&lt;0.05), while that in G2 and S phase decreased (P&lt;0.05); cellular senescence was accelerated (P&lt;0.01); ERK and its target proteins P-P90RSK and P-MEK were reduced while Bcl-2 family members increased. 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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&lt;0.001). When YAP was knocked down, the proliferation activity of h-PDLSCs was inhibited; the early &amp; late apoptosis rates increased; the proportion of cells in G1 phases increased (P&lt;0.05), while that in G2 and S phase decreased (P&lt;0.05); cellular senescence was accelerated (P&lt;0.01); ERK and its target proteins P-P90RSK and P-MEK were reduced while Bcl-2 family members increased. 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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&lt;0.001). When YAP was knocked down, the proliferation activity of h-PDLSCs was inhibited; the early &amp; late apoptosis rates increased; the proportion of cells in G1 phases increased (P&lt;0.05), while that in G2 and S phase decreased (P&lt;0.05); cellular senescence was accelerated (P&lt;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.</abstract><cop>Australia</cop><pub>Ivyspring International Publisher</pub><pmid>29104479</pmid><doi>10.7150/ijms.20504</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Adaptor Proteins, Signal Transducing - genetics
Adaptor Proteins, Signal Transducing - metabolism
Apoptosis
Cell Nucleus - metabolism
Cell Proliferation
Cells, Cultured
Cytoplasm - metabolism
Down-Regulation
Gene Knockdown Techniques
Humans
MAP Kinase Signaling System
Periodontal Ligament - cytology
Phosphoproteins - genetics
Phosphoproteins - metabolism
Protein-Serine-Threonine Kinases - metabolism
Proto-Oncogene Proteins c-bcl-2 - metabolism
Research Paper
RNA, Messenger
RNA, Small Interfering
Stem Cells - metabolism
Transcription Factors
Transfection
title 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
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