Effects of matrix metalloproteinases on the fate of mesenchymal stem cells
Mesenchymal stem cells (MSCs) have great potential as a source of cells for cell-based therapy because of their ability for self-renewal and differentiation into functional cells. Moreover, matrix metalloproteinases (MMPs) have a critical role in the differentiation of MSCs into different lineages....
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Veröffentlicht in: | Stem cell research & therapy 2016-09, Vol.7 (1), p.129-129, Article 129 |
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description | Mesenchymal stem cells (MSCs) have great potential as a source of cells for cell-based therapy because of their ability for self-renewal and differentiation into functional cells. Moreover, matrix metalloproteinases (MMPs) have a critical role in the differentiation of MSCs into different lineages. MSCs also interact with exogenous MMPs at their surface, and regulate the pericellular localization of MMP activities. The fate of MSCs is regulated by specific MMPs associated with a key cell lineage. Recent reports suggest the integration of MMPs in the differentiation, angiogenesis, proliferation, and migration of MSCs. These interactions are not fully understood and warrant further investigation, especially for their application as therapeutic tools to treat different diseases. Therefore, overexpression of a single MMP or tissue-specific inhibitor of metalloproteinase in MSCs may promote transdifferentiation into a specific cell lineage, which can be used for the treatment of some diseases. In this review, we critically discuss the identification of various MMPs and the signaling pathways that affect the differentiation, migration, angiogenesis, and proliferation of MSCs. |
doi_str_mv | 10.1186/s13287-016-0393-1 |
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Moreover, matrix metalloproteinases (MMPs) have a critical role in the differentiation of MSCs into different lineages. MSCs also interact with exogenous MMPs at their surface, and regulate the pericellular localization of MMP activities. The fate of MSCs is regulated by specific MMPs associated with a key cell lineage. Recent reports suggest the integration of MMPs in the differentiation, angiogenesis, proliferation, and migration of MSCs. These interactions are not fully understood and warrant further investigation, especially for their application as therapeutic tools to treat different diseases. Therefore, overexpression of a single MMP or tissue-specific inhibitor of metalloproteinase in MSCs may promote transdifferentiation into a specific cell lineage, which can be used for the treatment of some diseases. 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In this review, we critically discuss the identification of various MMPs and the signaling pathways that affect the differentiation, migration, angiogenesis, and proliferation of MSCs.</description><subject>Analysis</subject><subject>Animals</subject><subject>Cell Differentiation - physiology</subject><subject>Cell Lineage - physiology</subject><subject>Cell proliferation</subject><subject>Cell Transdifferentiation - physiology</subject><subject>Cell- and Tissue-Based Therapy - methods</subject><subject>Humans</subject><subject>Matrix Metalloproteinases - metabolism</subject><subject>Mesenchymal Stromal Cells - metabolism</subject><subject>Metalloproteins</subject><subject>Neovascularization</subject><subject>Review</subject><subject>Signal Transduction - physiology</subject><subject>Stem cells</subject><subject>Stem Cells - metabolism</subject><issn>1757-6512</issn><issn>1757-6512</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNptklFrFDEUhQdRbKn9Ab7IgCD6MDU3aZKZF6GUWisFQfsessnNTkpmsk4y0v57M25bd8XkISH3uyfcw6mq10BOAFrxMQGjrWwIiIawjjXwrDoEyWUjONDnO_eD6jilW1IWY4SI05fVAZUCqGDisPp64RyanOro6kHnyd_VA2YdQtxMMaMfdcJSHOvcY-10xj8gJhxNfz_oUKeMQ20whPSqeuF0SHj8cB5VN58vbs6_NNffLq_Oz64bIyjPjbNm5Yy0WlroutZ2iB0xhAlOLAdAysFSvrJCaiAOmeVCc7Ei0lgUQrOj6tNWdjOvBrQGxzzpoDaTH_R0r6L2ar8y-l6t4y_Fi1WthCLw_kFgij9nTFkNPi0T6BHjnBS00AGlsu0K-vYf9DbO01imKxQVshOEkb_UWgdUfnSx_GsWUXV2KrigLSGyUCf_ocq2OHgTR3S-vO81fNhrKEzGu7zWc0rq6sf3ffbdDtujDrlPMczZxzHtg7AFzRRTmtA9GQdELblS21ypYpZacqUWw97sOv7U8Zgi9hvjM8Yb</recordid><startdate>20160909</startdate><enddate>20160909</enddate><creator>Almalki, Sami G</creator><creator>Agrawal, Devendra K</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160909</creationdate><title>Effects of matrix metalloproteinases on the fate of mesenchymal stem cells</title><author>Almalki, Sami G ; 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Moreover, matrix metalloproteinases (MMPs) have a critical role in the differentiation of MSCs into different lineages. MSCs also interact with exogenous MMPs at their surface, and regulate the pericellular localization of MMP activities. The fate of MSCs is regulated by specific MMPs associated with a key cell lineage. Recent reports suggest the integration of MMPs in the differentiation, angiogenesis, proliferation, and migration of MSCs. These interactions are not fully understood and warrant further investigation, especially for their application as therapeutic tools to treat different diseases. Therefore, overexpression of a single MMP or tissue-specific inhibitor of metalloproteinase in MSCs may promote transdifferentiation into a specific cell lineage, which can be used for the treatment of some diseases. 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subjects | Analysis Animals Cell Differentiation - physiology Cell Lineage - physiology Cell proliferation Cell Transdifferentiation - physiology Cell- and Tissue-Based Therapy - methods Humans Matrix Metalloproteinases - metabolism Mesenchymal Stromal Cells - metabolism Metalloproteins Neovascularization Review Signal Transduction - physiology Stem cells Stem Cells - metabolism |
title | Effects of matrix metalloproteinases on the fate of mesenchymal stem cells |
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