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Downregulation of DAB2IP Promotes Mesenchymal-To-Neuroepithelial Transition and Neuronal Differentiation of Human Mesenchymal Stem Cells
The DOC-2/DAB2 interactive protein (DAB2IP) is a new member of the Ras GTPase–activating protein family. Recent studies have shown that, in addition to its tumor suppressive role in various tumors, DAB2IP also plays an important role in regulating neuronal migration and positioning during brain deve...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3779184/ https://www.ncbi.nlm.nih.gov/pubmed/24073285 http://dx.doi.org/10.1371/journal.pone.0075884 |
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author | Chang, Sunny Li-Yun Chou, Ruey-Hwang Zeng, Hong-Jie Lin, Yu-Hsuan Chiu, Tai-Yu Yang, De-Ming Hung, Shih-Chieh Lai, Chih-Ho Hsieh, Jer-Tsong Shyu, Woei-Cherng Yu, Yung-Luen |
author_facet | Chang, Sunny Li-Yun Chou, Ruey-Hwang Zeng, Hong-Jie Lin, Yu-Hsuan Chiu, Tai-Yu Yang, De-Ming Hung, Shih-Chieh Lai, Chih-Ho Hsieh, Jer-Tsong Shyu, Woei-Cherng Yu, Yung-Luen |
author_sort | Chang, Sunny Li-Yun |
collection | PubMed |
description | The DOC-2/DAB2 interactive protein (DAB2IP) is a new member of the Ras GTPase–activating protein family. Recent studies have shown that, in addition to its tumor suppressive role in various tumors, DAB2IP also plays an important role in regulating neuronal migration and positioning during brain development. In this study, we determined the roles of DAB2IP in the neuronal differentiation of human mesenchymal stem cells (hMSCs). We found that lentiviral short hairpin RNA (shRNA)-mediated knockdown of DAB2IP promoted the mesenchymal-to-neuroepithelial stem cell transition (MtNeST) and neuronal differentiation, which were accompanied by a reduction of cell proliferation but not apoptosis or cellular senescence. This suggests that DAB2IP plays an important role in the neuronal induction of hMSCs. Moreover, our finding that reduction of glycogen synthase kinase 3 beta (GSK3β) activity upon LiCl pretreatment inhibited both the MtNeST and production of MAP2-positive cells upon DAB2IP knockdown suggests that this transition is most likely mediated by regulation of the GSK3β signaling pathway. Our study demonstrates that DAB2IP participates in the first step of neuron induction of hMSCs, which implies a potentially important role for DAB2IP in the MtNeST during neurogenesis. |
format | Online Article Text |
id | pubmed-3779184 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37791842013-09-26 Downregulation of DAB2IP Promotes Mesenchymal-To-Neuroepithelial Transition and Neuronal Differentiation of Human Mesenchymal Stem Cells Chang, Sunny Li-Yun Chou, Ruey-Hwang Zeng, Hong-Jie Lin, Yu-Hsuan Chiu, Tai-Yu Yang, De-Ming Hung, Shih-Chieh Lai, Chih-Ho Hsieh, Jer-Tsong Shyu, Woei-Cherng Yu, Yung-Luen PLoS One Research Article The DOC-2/DAB2 interactive protein (DAB2IP) is a new member of the Ras GTPase–activating protein family. Recent studies have shown that, in addition to its tumor suppressive role in various tumors, DAB2IP also plays an important role in regulating neuronal migration and positioning during brain development. In this study, we determined the roles of DAB2IP in the neuronal differentiation of human mesenchymal stem cells (hMSCs). We found that lentiviral short hairpin RNA (shRNA)-mediated knockdown of DAB2IP promoted the mesenchymal-to-neuroepithelial stem cell transition (MtNeST) and neuronal differentiation, which were accompanied by a reduction of cell proliferation but not apoptosis or cellular senescence. This suggests that DAB2IP plays an important role in the neuronal induction of hMSCs. Moreover, our finding that reduction of glycogen synthase kinase 3 beta (GSK3β) activity upon LiCl pretreatment inhibited both the MtNeST and production of MAP2-positive cells upon DAB2IP knockdown suggests that this transition is most likely mediated by regulation of the GSK3β signaling pathway. Our study demonstrates that DAB2IP participates in the first step of neuron induction of hMSCs, which implies a potentially important role for DAB2IP in the MtNeST during neurogenesis. Public Library of Science 2013-09-20 /pmc/articles/PMC3779184/ /pubmed/24073285 http://dx.doi.org/10.1371/journal.pone.0075884 Text en © 2013 Chang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Chang, Sunny Li-Yun Chou, Ruey-Hwang Zeng, Hong-Jie Lin, Yu-Hsuan Chiu, Tai-Yu Yang, De-Ming Hung, Shih-Chieh Lai, Chih-Ho Hsieh, Jer-Tsong Shyu, Woei-Cherng Yu, Yung-Luen Downregulation of DAB2IP Promotes Mesenchymal-To-Neuroepithelial Transition and Neuronal Differentiation of Human Mesenchymal Stem Cells |
title | Downregulation of DAB2IP Promotes Mesenchymal-To-Neuroepithelial Transition and Neuronal Differentiation of Human Mesenchymal Stem Cells |
title_full | Downregulation of DAB2IP Promotes Mesenchymal-To-Neuroepithelial Transition and Neuronal Differentiation of Human Mesenchymal Stem Cells |
title_fullStr | Downregulation of DAB2IP Promotes Mesenchymal-To-Neuroepithelial Transition and Neuronal Differentiation of Human Mesenchymal Stem Cells |
title_full_unstemmed | Downregulation of DAB2IP Promotes Mesenchymal-To-Neuroepithelial Transition and Neuronal Differentiation of Human Mesenchymal Stem Cells |
title_short | Downregulation of DAB2IP Promotes Mesenchymal-To-Neuroepithelial Transition and Neuronal Differentiation of Human Mesenchymal Stem Cells |
title_sort | downregulation of dab2ip promotes mesenchymal-to-neuroepithelial transition and neuronal differentiation of human mesenchymal stem cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3779184/ https://www.ncbi.nlm.nih.gov/pubmed/24073285 http://dx.doi.org/10.1371/journal.pone.0075884 |
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