author_facet Gu, Ke
Fu, Xucheng
Tian, Hui
Zhang, Yafei
Li, Aonan
Wang, Ying
Wen, Yong
Gu, Weiting
Gu, Ke
Fu, Xucheng
Tian, Hui
Zhang, Yafei
Li, Aonan
Wang, Ying
Wen, Yong
Gu, Weiting
author Gu, Ke
Fu, Xucheng
Tian, Hui
Zhang, Yafei
Li, Aonan
Wang, Ying
Wen, Yong
Gu, Weiting
spellingShingle Gu, Ke
Fu, Xucheng
Tian, Hui
Zhang, Yafei
Li, Aonan
Wang, Ying
Wen, Yong
Gu, Weiting
Journal of Cellular Biochemistry
TAZ promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐SMAD3
Cell Biology
Molecular Biology
Biochemistry
author_sort gu, ke
spelling Gu, Ke Fu, Xucheng Tian, Hui Zhang, Yafei Li, Aonan Wang, Ying Wen, Yong Gu, Weiting 0730-2312 1097-4644 Wiley Cell Biology Molecular Biology Biochemistry http://dx.doi.org/10.1002/jcb.29346 <jats:title>Abstract</jats:title><jats:sec><jats:title>Objective</jats:title><jats:p>This study aims to offer insights about the biological influence of TAZ, which is a transcriptional coactivator containing a PDZ‐binding motif, upon the apoptosis, proliferation, and osteogenic differentiation of human periodontal ligament stem cells (h‐PDLSCs).</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>We used the green fluorescence protein lentivirus infection system to knockdown or overexpress TAZ in h‐PDLSCs. 5‐ethynyl‐2’‐deoxyuridine (EdU) staining detected the proliferative activity, and h‐PDLSC apoptosis was analyzed by Annexin V‐APC staining. TAZ knockdown or overexpression was performed to determine the osteogenic differentiation function of TAZ during the osteogenic induction of h‐PDLSCs. The molecular mechanism of TAZ in the promotion of h‐PDLSC osteogenesis was also explored. The chemical inhibitor of SMAD2/3 SIS3 HCL was used to identify the effects in vitro osteogenic differentiation and bone formation in h‐PDLSCs overexpressing TAZ.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>TAZ overexpression resulted in enhanced cell rapid multiplication, which increased the expression of messenger RNA in stemness‐related genes. By comparison, TAZ knockdown reduced proliferative activity and increased the apoptosis of h‐PDLSCs. After the 7‐day osteogenic induction period, alkaline phosphatase activity in the TAZ‐overexpression group was significantly increased, and mineralized nodules increased significantly after osteogenic induction for 21 days. Similarly, osteoblast differentiation of h‐PDLSCs was impaired after TAZ knockdown. However, the osteogenic potential of the group exposed to the p‐SMAD3 inhibitor was restored to its original level.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>Hippo/TAZ plays a positive role inside the proliferation, stemness maintenance, and osteogenic specialization of h‐PDLSCs, and the specific downstream factor of osteogenic differentiation is SMAD3.</jats:p></jats:sec> TAZ promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐SMAD3 Journal of Cellular Biochemistry
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Chemie und Pharmazie
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recordtype ai
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series Journal of Cellular Biochemistry
source_id 49
title TAZ promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐SMAD3
title_unstemmed TAZ promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐SMAD3
title_full TAZ promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐SMAD3
title_fullStr TAZ promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐SMAD3
title_full_unstemmed TAZ promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐SMAD3
title_short TAZ promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐SMAD3
title_sort taz promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐smad3
topic Cell Biology
Molecular Biology
Biochemistry
url http://dx.doi.org/10.1002/jcb.29346
publishDate 2020
physical 1101-1113
description <jats:title>Abstract</jats:title><jats:sec><jats:title>Objective</jats:title><jats:p>This study aims to offer insights about the biological influence of TAZ, which is a transcriptional coactivator containing a PDZ‐binding motif, upon the apoptosis, proliferation, and osteogenic differentiation of human periodontal ligament stem cells (h‐PDLSCs).</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>We used the green fluorescence protein lentivirus infection system to knockdown or overexpress TAZ in h‐PDLSCs. 5‐ethynyl‐2’‐deoxyuridine (EdU) staining detected the proliferative activity, and h‐PDLSC apoptosis was analyzed by Annexin V‐APC staining. TAZ knockdown or overexpression was performed to determine the osteogenic differentiation function of TAZ during the osteogenic induction of h‐PDLSCs. The molecular mechanism of TAZ in the promotion of h‐PDLSC osteogenesis was also explored. The chemical inhibitor of SMAD2/3 SIS3 HCL was used to identify the effects in vitro osteogenic differentiation and bone formation in h‐PDLSCs overexpressing TAZ.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>TAZ overexpression resulted in enhanced cell rapid multiplication, which increased the expression of messenger RNA in stemness‐related genes. By comparison, TAZ knockdown reduced proliferative activity and increased the apoptosis of h‐PDLSCs. After the 7‐day osteogenic induction period, alkaline phosphatase activity in the TAZ‐overexpression group was significantly increased, and mineralized nodules increased significantly after osteogenic induction for 21 days. Similarly, osteoblast differentiation of h‐PDLSCs was impaired after TAZ knockdown. However, the osteogenic potential of the group exposed to the p‐SMAD3 inhibitor was restored to its original level.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>Hippo/TAZ plays a positive role inside the proliferation, stemness maintenance, and osteogenic specialization of h‐PDLSCs, and the specific downstream factor of osteogenic differentiation is SMAD3.</jats:p></jats:sec>
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author Gu, Ke, Fu, Xucheng, Tian, Hui, Zhang, Yafei, Li, Aonan, Wang, Ying, Wen, Yong, Gu, Weiting
author_facet Gu, Ke, Fu, Xucheng, Tian, Hui, Zhang, Yafei, Li, Aonan, Wang, Ying, Wen, Yong, Gu, Weiting, Gu, Ke, Fu, Xucheng, Tian, Hui, Zhang, Yafei, Li, Aonan, Wang, Ying, Wen, Yong, Gu, Weiting
author_sort gu, ke
container_issue 2
container_start_page 1101
container_title Journal of Cellular Biochemistry
container_volume 121
description <jats:title>Abstract</jats:title><jats:sec><jats:title>Objective</jats:title><jats:p>This study aims to offer insights about the biological influence of TAZ, which is a transcriptional coactivator containing a PDZ‐binding motif, upon the apoptosis, proliferation, and osteogenic differentiation of human periodontal ligament stem cells (h‐PDLSCs).</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>We used the green fluorescence protein lentivirus infection system to knockdown or overexpress TAZ in h‐PDLSCs. 5‐ethynyl‐2’‐deoxyuridine (EdU) staining detected the proliferative activity, and h‐PDLSC apoptosis was analyzed by Annexin V‐APC staining. TAZ knockdown or overexpression was performed to determine the osteogenic differentiation function of TAZ during the osteogenic induction of h‐PDLSCs. The molecular mechanism of TAZ in the promotion of h‐PDLSC osteogenesis was also explored. The chemical inhibitor of SMAD2/3 SIS3 HCL was used to identify the effects in vitro osteogenic differentiation and bone formation in h‐PDLSCs overexpressing TAZ.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>TAZ overexpression resulted in enhanced cell rapid multiplication, which increased the expression of messenger RNA in stemness‐related genes. By comparison, TAZ knockdown reduced proliferative activity and increased the apoptosis of h‐PDLSCs. After the 7‐day osteogenic induction period, alkaline phosphatase activity in the TAZ‐overexpression group was significantly increased, and mineralized nodules increased significantly after osteogenic induction for 21 days. Similarly, osteoblast differentiation of h‐PDLSCs was impaired after TAZ knockdown. However, the osteogenic potential of the group exposed to the p‐SMAD3 inhibitor was restored to its original level.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>Hippo/TAZ plays a positive role inside the proliferation, stemness maintenance, and osteogenic specialization of h‐PDLSCs, and the specific downstream factor of osteogenic differentiation is SMAD3.</jats:p></jats:sec>
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spelling Gu, Ke Fu, Xucheng Tian, Hui Zhang, Yafei Li, Aonan Wang, Ying Wen, Yong Gu, Weiting 0730-2312 1097-4644 Wiley Cell Biology Molecular Biology Biochemistry http://dx.doi.org/10.1002/jcb.29346 <jats:title>Abstract</jats:title><jats:sec><jats:title>Objective</jats:title><jats:p>This study aims to offer insights about the biological influence of TAZ, which is a transcriptional coactivator containing a PDZ‐binding motif, upon the apoptosis, proliferation, and osteogenic differentiation of human periodontal ligament stem cells (h‐PDLSCs).</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>We used the green fluorescence protein lentivirus infection system to knockdown or overexpress TAZ in h‐PDLSCs. 5‐ethynyl‐2’‐deoxyuridine (EdU) staining detected the proliferative activity, and h‐PDLSC apoptosis was analyzed by Annexin V‐APC staining. TAZ knockdown or overexpression was performed to determine the osteogenic differentiation function of TAZ during the osteogenic induction of h‐PDLSCs. The molecular mechanism of TAZ in the promotion of h‐PDLSC osteogenesis was also explored. The chemical inhibitor of SMAD2/3 SIS3 HCL was used to identify the effects in vitro osteogenic differentiation and bone formation in h‐PDLSCs overexpressing TAZ.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>TAZ overexpression resulted in enhanced cell rapid multiplication, which increased the expression of messenger RNA in stemness‐related genes. By comparison, TAZ knockdown reduced proliferative activity and increased the apoptosis of h‐PDLSCs. After the 7‐day osteogenic induction period, alkaline phosphatase activity in the TAZ‐overexpression group was significantly increased, and mineralized nodules increased significantly after osteogenic induction for 21 days. Similarly, osteoblast differentiation of h‐PDLSCs was impaired after TAZ knockdown. However, the osteogenic potential of the group exposed to the p‐SMAD3 inhibitor was restored to its original level.</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>Hippo/TAZ plays a positive role inside the proliferation, stemness maintenance, and osteogenic specialization of h‐PDLSCs, and the specific downstream factor of osteogenic differentiation is SMAD3.</jats:p></jats:sec> TAZ promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐SMAD3 Journal of Cellular Biochemistry
spellingShingle Gu, Ke, Fu, Xucheng, Tian, Hui, Zhang, Yafei, Li, Aonan, Wang, Ying, Wen, Yong, Gu, Weiting, Journal of Cellular Biochemistry, TAZ promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐SMAD3, Cell Biology, Molecular Biology, Biochemistry
title TAZ promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐SMAD3
title_full TAZ promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐SMAD3
title_fullStr TAZ promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐SMAD3
title_full_unstemmed TAZ promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐SMAD3
title_short TAZ promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐SMAD3
title_sort taz promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐smad3
title_unstemmed TAZ promotes the proliferation and osteogenic differentiation of human periodontal ligament stem cells via the p‐SMAD3
topic Cell Biology, Molecular Biology, Biochemistry
url http://dx.doi.org/10.1002/jcb.29346