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Enhancement of Matrix Metalloproteinase-2 (MMP-2) as a Potential Chondrogenic Marker during Chondrogenic Differentiation of Human Adipose-Derived Stem Cells

Human adipose-derived stem cells (hASCs) have a capacity to undergo adipogenic, chondrogenic, and osteogenic differentiation. Recently, hASCs were applied to various fields including cell therapy for tissue regeneration. However, it is hard to predict the direction of differentiation of hASCs in rea...

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Autores principales: Arai, Yoshie, Park, Sunghyun, Choi, Bogyu, Ko, Kyoung-Won, Choi, Won Chul, Lee, Joong-Myung, Han, Dong-Wook, Park, Hun-Kuk, Han, Inbo, Lee, Jong Hun, Lee, Soo-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4926495/
https://www.ncbi.nlm.nih.gov/pubmed/27322256
http://dx.doi.org/10.3390/ijms17060963
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author Arai, Yoshie
Park, Sunghyun
Choi, Bogyu
Ko, Kyoung-Won
Choi, Won Chul
Lee, Joong-Myung
Han, Dong-Wook
Park, Hun-Kuk
Han, Inbo
Lee, Jong Hun
Lee, Soo-Hong
author_facet Arai, Yoshie
Park, Sunghyun
Choi, Bogyu
Ko, Kyoung-Won
Choi, Won Chul
Lee, Joong-Myung
Han, Dong-Wook
Park, Hun-Kuk
Han, Inbo
Lee, Jong Hun
Lee, Soo-Hong
author_sort Arai, Yoshie
collection PubMed
description Human adipose-derived stem cells (hASCs) have a capacity to undergo adipogenic, chondrogenic, and osteogenic differentiation. Recently, hASCs were applied to various fields including cell therapy for tissue regeneration. However, it is hard to predict the direction of differentiation of hASCs in real-time. Matrix metalloproteinases (MMPs) are one family of proteolytic enzymes that plays a pivotal role in regulating the biology of stem cells. MMPs secreted by hASCs are expected to show different expression patterns depending on the differentiation state of hASCs because biological functions exhibit different patterns during the differentiation of stem cells. Here, we investigated proteolytic enzyme activity, especially MMP-2 activity, in hASCs during their differentiation. The activities of proteolytic enzymes and MMP-2 were higher during chondrogenic differentiation than during adipogenic and osteogenic differentiation. During chondrogenic differentiation, mRNA expression of MMP-2 and the level of the active form of MMP-2 were increased, which also correlated with Col II. It is concluded that proteolytic enzyme activity and the level of the active form of MMP-2 were increased during chondrogenic differentiation, which was accelerated in the presence of Col II protein. According to our findings, MMP-2 could be a candidate maker for real-time detection of chondrogenic differentiation of hASCs.
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spelling pubmed-49264952016-07-06 Enhancement of Matrix Metalloproteinase-2 (MMP-2) as a Potential Chondrogenic Marker during Chondrogenic Differentiation of Human Adipose-Derived Stem Cells Arai, Yoshie Park, Sunghyun Choi, Bogyu Ko, Kyoung-Won Choi, Won Chul Lee, Joong-Myung Han, Dong-Wook Park, Hun-Kuk Han, Inbo Lee, Jong Hun Lee, Soo-Hong Int J Mol Sci Article Human adipose-derived stem cells (hASCs) have a capacity to undergo adipogenic, chondrogenic, and osteogenic differentiation. Recently, hASCs were applied to various fields including cell therapy for tissue regeneration. However, it is hard to predict the direction of differentiation of hASCs in real-time. Matrix metalloproteinases (MMPs) are one family of proteolytic enzymes that plays a pivotal role in regulating the biology of stem cells. MMPs secreted by hASCs are expected to show different expression patterns depending on the differentiation state of hASCs because biological functions exhibit different patterns during the differentiation of stem cells. Here, we investigated proteolytic enzyme activity, especially MMP-2 activity, in hASCs during their differentiation. The activities of proteolytic enzymes and MMP-2 were higher during chondrogenic differentiation than during adipogenic and osteogenic differentiation. During chondrogenic differentiation, mRNA expression of MMP-2 and the level of the active form of MMP-2 were increased, which also correlated with Col II. It is concluded that proteolytic enzyme activity and the level of the active form of MMP-2 were increased during chondrogenic differentiation, which was accelerated in the presence of Col II protein. According to our findings, MMP-2 could be a candidate maker for real-time detection of chondrogenic differentiation of hASCs. MDPI 2016-06-17 /pmc/articles/PMC4926495/ /pubmed/27322256 http://dx.doi.org/10.3390/ijms17060963 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Arai, Yoshie
Park, Sunghyun
Choi, Bogyu
Ko, Kyoung-Won
Choi, Won Chul
Lee, Joong-Myung
Han, Dong-Wook
Park, Hun-Kuk
Han, Inbo
Lee, Jong Hun
Lee, Soo-Hong
Enhancement of Matrix Metalloproteinase-2 (MMP-2) as a Potential Chondrogenic Marker during Chondrogenic Differentiation of Human Adipose-Derived Stem Cells
title Enhancement of Matrix Metalloproteinase-2 (MMP-2) as a Potential Chondrogenic Marker during Chondrogenic Differentiation of Human Adipose-Derived Stem Cells
title_full Enhancement of Matrix Metalloproteinase-2 (MMP-2) as a Potential Chondrogenic Marker during Chondrogenic Differentiation of Human Adipose-Derived Stem Cells
title_fullStr Enhancement of Matrix Metalloproteinase-2 (MMP-2) as a Potential Chondrogenic Marker during Chondrogenic Differentiation of Human Adipose-Derived Stem Cells
title_full_unstemmed Enhancement of Matrix Metalloproteinase-2 (MMP-2) as a Potential Chondrogenic Marker during Chondrogenic Differentiation of Human Adipose-Derived Stem Cells
title_short Enhancement of Matrix Metalloproteinase-2 (MMP-2) as a Potential Chondrogenic Marker during Chondrogenic Differentiation of Human Adipose-Derived Stem Cells
title_sort enhancement of matrix metalloproteinase-2 (mmp-2) as a potential chondrogenic marker during chondrogenic differentiation of human adipose-derived stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4926495/
https://www.ncbi.nlm.nih.gov/pubmed/27322256
http://dx.doi.org/10.3390/ijms17060963
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