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MEST Regulates the Stemness of Human Periodontal Ligament Stem Cells
Periodontal ligament (PDL) stem cells (PDLSCs) have been reported as a useful cell source for periodontal tissue regeneration. However, one of the issues is the difficulty of obtaining a sufficient number of PDLSCs for clinical application because very few PDLSCs can be isolated from PDL tissue of d...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7366229/ https://www.ncbi.nlm.nih.gov/pubmed/32724317 http://dx.doi.org/10.1155/2020/9672673 |
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author | Hasegawa, Daigaku Hasegawa, Kana Kaneko, Hiroshi Yoshida, Shinichiro Mitarai, Hiromi Arima, Mai Tomokiyo, Atsushi Hamano, Sayuri Sugii, Hideki Wada, Naohisa Kiyoshima, Tamotsu Maeda, Hidefumi |
author_facet | Hasegawa, Daigaku Hasegawa, Kana Kaneko, Hiroshi Yoshida, Shinichiro Mitarai, Hiromi Arima, Mai Tomokiyo, Atsushi Hamano, Sayuri Sugii, Hideki Wada, Naohisa Kiyoshima, Tamotsu Maeda, Hidefumi |
author_sort | Hasegawa, Daigaku |
collection | PubMed |
description | Periodontal ligament (PDL) stem cells (PDLSCs) have been reported as a useful cell source for periodontal tissue regeneration. However, one of the issues is the difficulty of obtaining a sufficient number of PDLSCs for clinical application because very few PDLSCs can be isolated from PDL tissue of donors. Therefore, we aimed to identify a specific factor that converts human PDL cells into stem-like cells. In this study, microarray analysis comparing the gene profiles of human PDLSC lines (2-14 and 2-23) with those of a cell line with a low differentiation potential (2-52) identified the imprinted gene mesoderm-specific transcript (MEST). MEST was expressed in the cytoplasm of 2-23 cells. Knockdown of MEST by siRNA in 2-23 cells inhibited the expression of stem cell markers, such as CD105, CD146, p75NTR, N-cadherin, and NANOG; the proliferative potential; and multidifferentiation capacity for osteoblasts, adipocytes, and chondrocytes. On the other hand, overexpression of MEST in 2-52 cells enhanced the expression of stem cell markers and PDL-related markers and the multidifferentiation capacity. In addition, MEST-overexpressing 2-52 cells exhibited a change in morphology from a spindle shape to a stem cell-like round shape that was similar to 2-14 and 2-23 cell morphologies. These results suggest that MEST plays a critical role in the maintenance of stemness in PDLSCs and converts PDL cells into PDLSC-like cells. Therefore, this study indicates that MEST may be a therapeutic factor for periodontal tissue regeneration by inducing PDLSCs. |
format | Online Article Text |
id | pubmed-7366229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-73662292020-07-27 MEST Regulates the Stemness of Human Periodontal Ligament Stem Cells Hasegawa, Daigaku Hasegawa, Kana Kaneko, Hiroshi Yoshida, Shinichiro Mitarai, Hiromi Arima, Mai Tomokiyo, Atsushi Hamano, Sayuri Sugii, Hideki Wada, Naohisa Kiyoshima, Tamotsu Maeda, Hidefumi Stem Cells Int Research Article Periodontal ligament (PDL) stem cells (PDLSCs) have been reported as a useful cell source for periodontal tissue regeneration. However, one of the issues is the difficulty of obtaining a sufficient number of PDLSCs for clinical application because very few PDLSCs can be isolated from PDL tissue of donors. Therefore, we aimed to identify a specific factor that converts human PDL cells into stem-like cells. In this study, microarray analysis comparing the gene profiles of human PDLSC lines (2-14 and 2-23) with those of a cell line with a low differentiation potential (2-52) identified the imprinted gene mesoderm-specific transcript (MEST). MEST was expressed in the cytoplasm of 2-23 cells. Knockdown of MEST by siRNA in 2-23 cells inhibited the expression of stem cell markers, such as CD105, CD146, p75NTR, N-cadherin, and NANOG; the proliferative potential; and multidifferentiation capacity for osteoblasts, adipocytes, and chondrocytes. On the other hand, overexpression of MEST in 2-52 cells enhanced the expression of stem cell markers and PDL-related markers and the multidifferentiation capacity. In addition, MEST-overexpressing 2-52 cells exhibited a change in morphology from a spindle shape to a stem cell-like round shape that was similar to 2-14 and 2-23 cell morphologies. These results suggest that MEST plays a critical role in the maintenance of stemness in PDLSCs and converts PDL cells into PDLSC-like cells. Therefore, this study indicates that MEST may be a therapeutic factor for periodontal tissue regeneration by inducing PDLSCs. Hindawi 2020-07-08 /pmc/articles/PMC7366229/ /pubmed/32724317 http://dx.doi.org/10.1155/2020/9672673 Text en Copyright © 2020 Daigaku Hasegawa et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Hasegawa, Daigaku Hasegawa, Kana Kaneko, Hiroshi Yoshida, Shinichiro Mitarai, Hiromi Arima, Mai Tomokiyo, Atsushi Hamano, Sayuri Sugii, Hideki Wada, Naohisa Kiyoshima, Tamotsu Maeda, Hidefumi MEST Regulates the Stemness of Human Periodontal Ligament Stem Cells |
title | MEST Regulates the Stemness of Human Periodontal Ligament Stem Cells |
title_full | MEST Regulates the Stemness of Human Periodontal Ligament Stem Cells |
title_fullStr | MEST Regulates the Stemness of Human Periodontal Ligament Stem Cells |
title_full_unstemmed | MEST Regulates the Stemness of Human Periodontal Ligament Stem Cells |
title_short | MEST Regulates the Stemness of Human Periodontal Ligament Stem Cells |
title_sort | mest regulates the stemness of human periodontal ligament stem cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7366229/ https://www.ncbi.nlm.nih.gov/pubmed/32724317 http://dx.doi.org/10.1155/2020/9672673 |
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