Mesenchymal stem cells' interaction with skin: Wound-healing effect on fibroblast cells and skin tissue
ABSTRACT Mesenchymal stem cells (MSCs) are multipotent progenitor cells with the ability to secrete growth factors. Because wound healing is associated with fibroblast cells and extracellular matrix (ECM) in the dermis and epidermis, we used fibroblast cells to resolve the question of whether or not...
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Veröffentlicht in: | Wound repair and regeneration 2010-11, Vol.18 (6), p.655-661 |
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creator | Jeon, Young Keul Jang, Yun Ho Yoo, Dong Ryeol Kim, Si Na Lee, Sang Koo Nam, Myeong Jin |
description | ABSTRACT
Mesenchymal stem cells (MSCs) are multipotent progenitor cells with the ability to secrete growth factors. Because wound healing is associated with fibroblast cells and extracellular matrix (ECM) in the dermis and epidermis, we used fibroblast cells to resolve the question of whether or not MSCs regulate wound healing in vitro via a regenerative function. Using a cell proliferation assay, we demonstrated that conditioned media (CM) obtained from MSCs significantly enhanced the cell survival ability of fibroblast cells. Moreover, by measurement of mRNA and protein, we observed that CM also promoted the production or secretion of collagen, elastin, and fibronectin. To better understand the effects of ECM‐related wound healing, we measured the level of collagen‐degradative enzyme (matrix metalloprotease‐1), and observed that CM suppressed matrix metalloprotease‐1 expression. For the determination of oxidative stress, which has an influence on wound healing, we performed the superoxide dismutase and glutathione peroxidase assays; our results suggested that CM inhibited the oxidative stress of fibroblast cells. In order to widely investigate the wound‐healing effects of MSCs, we performed in vivo experiments, and observed that MSCs stimulated wound healing. In summary, the results of this study suggest that MSCs inhibit the loss of fibroblast cells and ECM, and accumulation of oxidative stress. We found that MSCs stimulate wound healing in vitro and in vivo, suggesting that MSCs have the potential to enhance wound healing. |
doi_str_mv | 10.1111/j.1524-475X.2010.00636.x |
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Mesenchymal stem cells (MSCs) are multipotent progenitor cells with the ability to secrete growth factors. Because wound healing is associated with fibroblast cells and extracellular matrix (ECM) in the dermis and epidermis, we used fibroblast cells to resolve the question of whether or not MSCs regulate wound healing in vitro via a regenerative function. Using a cell proliferation assay, we demonstrated that conditioned media (CM) obtained from MSCs significantly enhanced the cell survival ability of fibroblast cells. Moreover, by measurement of mRNA and protein, we observed that CM also promoted the production or secretion of collagen, elastin, and fibronectin. To better understand the effects of ECM‐related wound healing, we measured the level of collagen‐degradative enzyme (matrix metalloprotease‐1), and observed that CM suppressed matrix metalloprotease‐1 expression. For the determination of oxidative stress, which has an influence on wound healing, we performed the superoxide dismutase and glutathione peroxidase assays; our results suggested that CM inhibited the oxidative stress of fibroblast cells. In order to widely investigate the wound‐healing effects of MSCs, we performed in vivo experiments, and observed that MSCs stimulated wound healing. In summary, the results of this study suggest that MSCs inhibit the loss of fibroblast cells and ECM, and accumulation of oxidative stress. We found that MSCs stimulate wound healing in vitro and in vivo, suggesting that MSCs have the potential to enhance wound healing.</description><identifier>ISSN: 1067-1927</identifier><identifier>EISSN: 1524-475X</identifier><identifier>DOI: 10.1111/j.1524-475X.2010.00636.x</identifier><identifier>PMID: 20955344</identifier><language>eng</language><publisher>Malden, USA: Blackwell Publishing Inc</publisher><subject>Animals ; Cell Movement ; Cell Proliferation ; Cell survival ; Collagen ; Collagen - metabolism ; Culture Media, Conditioned ; Dermis ; Elastin ; Elastin - metabolism ; Enzymes ; Epidermis ; Extracellular matrix ; Fibroblasts ; Fibroblasts - metabolism ; Fibronectin ; Fibronectins - metabolism ; Glutathione peroxidase ; Glutathione Peroxidase - metabolism ; Growth factors ; In Vitro Techniques ; Male ; Matrix Metalloproteinase 1 - metabolism ; Mesenchymal Stromal Cells - physiology ; Mesenchyme ; mRNA ; Oxidative Stress ; Rats ; Rats, Sprague-Dawley ; Secretion ; Skin ; Skin - cytology ; Skin - injuries ; Stem cells ; Superoxide dismutase ; Superoxide Dismutase - metabolism ; Wound Healing</subject><ispartof>Wound repair and regeneration, 2010-11, Vol.18 (6), p.655-661</ispartof><rights>2010 by the Wound Healing Society</rights><rights>2010 by the Wound Healing Society.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5226-7efdbf1562fb60196b7cf7aa891b910d128f3027aefaaa406c61238c0e4dacf63</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1524-475X.2010.00636.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1524-475X.2010.00636.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20955344$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jeon, Young Keul</creatorcontrib><creatorcontrib>Jang, Yun Ho</creatorcontrib><creatorcontrib>Yoo, Dong Ryeol</creatorcontrib><creatorcontrib>Kim, Si Na</creatorcontrib><creatorcontrib>Lee, Sang Koo</creatorcontrib><creatorcontrib>Nam, Myeong Jin</creatorcontrib><title>Mesenchymal stem cells' interaction with skin: Wound-healing effect on fibroblast cells and skin tissue</title><title>Wound repair and regeneration</title><addtitle>Wound Repair Regen</addtitle><description>ABSTRACT
Mesenchymal stem cells (MSCs) are multipotent progenitor cells with the ability to secrete growth factors. Because wound healing is associated with fibroblast cells and extracellular matrix (ECM) in the dermis and epidermis, we used fibroblast cells to resolve the question of whether or not MSCs regulate wound healing in vitro via a regenerative function. Using a cell proliferation assay, we demonstrated that conditioned media (CM) obtained from MSCs significantly enhanced the cell survival ability of fibroblast cells. Moreover, by measurement of mRNA and protein, we observed that CM also promoted the production or secretion of collagen, elastin, and fibronectin. To better understand the effects of ECM‐related wound healing, we measured the level of collagen‐degradative enzyme (matrix metalloprotease‐1), and observed that CM suppressed matrix metalloprotease‐1 expression. For the determination of oxidative stress, which has an influence on wound healing, we performed the superoxide dismutase and glutathione peroxidase assays; our results suggested that CM inhibited the oxidative stress of fibroblast cells. In order to widely investigate the wound‐healing effects of MSCs, we performed in vivo experiments, and observed that MSCs stimulated wound healing. In summary, the results of this study suggest that MSCs inhibit the loss of fibroblast cells and ECM, and accumulation of oxidative stress. We found that MSCs stimulate wound healing in vitro and in vivo, suggesting that MSCs have the potential to enhance wound healing.</description><subject>Animals</subject><subject>Cell Movement</subject><subject>Cell Proliferation</subject><subject>Cell survival</subject><subject>Collagen</subject><subject>Collagen - metabolism</subject><subject>Culture Media, Conditioned</subject><subject>Dermis</subject><subject>Elastin</subject><subject>Elastin - metabolism</subject><subject>Enzymes</subject><subject>Epidermis</subject><subject>Extracellular matrix</subject><subject>Fibroblasts</subject><subject>Fibroblasts - metabolism</subject><subject>Fibronectin</subject><subject>Fibronectins - metabolism</subject><subject>Glutathione peroxidase</subject><subject>Glutathione Peroxidase - metabolism</subject><subject>Growth factors</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Matrix Metalloproteinase 1 - metabolism</subject><subject>Mesenchymal Stromal Cells - physiology</subject><subject>Mesenchyme</subject><subject>mRNA</subject><subject>Oxidative Stress</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Secretion</subject><subject>Skin</subject><subject>Skin - cytology</subject><subject>Skin - injuries</subject><subject>Stem cells</subject><subject>Superoxide dismutase</subject><subject>Superoxide Dismutase - metabolism</subject><subject>Wound Healing</subject><issn>1067-1927</issn><issn>1524-475X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi1ERT_gLyDfesp27MR2grigiraIbZFWQHqzHGfc9TYfJU7U3X-P0y17xRePPM87suYhhDJYsHguNgsmeJZkStwvOMRXAJnKxfYNOTk03sYapEpYwdUxOQ1hAwBCFPk7csyhECLNshPycIsBO7vetaahYcSWWmyacE59N-Jg7Oj7jj77cU3Do-8-0bKfujpZo2l890DRObQjjYjz1dBXjQnjfgA1Xf0SoaMPYcL35MiZJuCH1_uM_Lr6-vPyJln-uP52-WWZWMG5TBS6unJMSO4qCayQlbJOGZMXrCoY1IznLgWuDDpjTAbSSsbT3AJmtbFOpmfkfD_3aej_TBhG3fow_8h02E9BFyKTEJfwfzLnLK6WZXkkP76SU9VirZ8G35php_9tMQKf98Czb3B36DPQsy290bMUPUvRsy39YktvdblaxSLGk33cRwHbQ9wMj1qqVAld3l3r29_lslx9B32f_gWDTZil</recordid><startdate>201011</startdate><enddate>201011</enddate><creator>Jeon, Young Keul</creator><creator>Jang, Yun Ho</creator><creator>Yoo, Dong Ryeol</creator><creator>Kim, Si Na</creator><creator>Lee, Sang Koo</creator><creator>Nam, Myeong Jin</creator><general>Blackwell Publishing Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>201011</creationdate><title>Mesenchymal stem cells' interaction with skin: Wound-healing effect on fibroblast cells and skin tissue</title><author>Jeon, Young Keul ; Jang, Yun Ho ; Yoo, Dong Ryeol ; Kim, Si Na ; Lee, Sang Koo ; Nam, Myeong Jin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5226-7efdbf1562fb60196b7cf7aa891b910d128f3027aefaaa406c61238c0e4dacf63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Cell Movement</topic><topic>Cell Proliferation</topic><topic>Cell survival</topic><topic>Collagen</topic><topic>Collagen - metabolism</topic><topic>Culture Media, Conditioned</topic><topic>Dermis</topic><topic>Elastin</topic><topic>Elastin - metabolism</topic><topic>Enzymes</topic><topic>Epidermis</topic><topic>Extracellular matrix</topic><topic>Fibroblasts</topic><topic>Fibroblasts - metabolism</topic><topic>Fibronectin</topic><topic>Fibronectins - metabolism</topic><topic>Glutathione peroxidase</topic><topic>Glutathione Peroxidase - metabolism</topic><topic>Growth factors</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Matrix Metalloproteinase 1 - metabolism</topic><topic>Mesenchymal Stromal Cells - physiology</topic><topic>Mesenchyme</topic><topic>mRNA</topic><topic>Oxidative Stress</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Secretion</topic><topic>Skin</topic><topic>Skin - cytology</topic><topic>Skin - injuries</topic><topic>Stem cells</topic><topic>Superoxide dismutase</topic><topic>Superoxide Dismutase - metabolism</topic><topic>Wound Healing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jeon, Young Keul</creatorcontrib><creatorcontrib>Jang, Yun Ho</creatorcontrib><creatorcontrib>Yoo, Dong Ryeol</creatorcontrib><creatorcontrib>Kim, Si Na</creatorcontrib><creatorcontrib>Lee, Sang Koo</creatorcontrib><creatorcontrib>Nam, Myeong Jin</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Wound repair and regeneration</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jeon, Young Keul</au><au>Jang, Yun Ho</au><au>Yoo, Dong Ryeol</au><au>Kim, Si Na</au><au>Lee, Sang Koo</au><au>Nam, Myeong Jin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mesenchymal stem cells' interaction with skin: Wound-healing effect on fibroblast cells and skin tissue</atitle><jtitle>Wound repair and regeneration</jtitle><addtitle>Wound Repair Regen</addtitle><date>2010-11</date><risdate>2010</risdate><volume>18</volume><issue>6</issue><spage>655</spage><epage>661</epage><pages>655-661</pages><issn>1067-1927</issn><eissn>1524-475X</eissn><abstract>ABSTRACT
Mesenchymal stem cells (MSCs) are multipotent progenitor cells with the ability to secrete growth factors. Because wound healing is associated with fibroblast cells and extracellular matrix (ECM) in the dermis and epidermis, we used fibroblast cells to resolve the question of whether or not MSCs regulate wound healing in vitro via a regenerative function. Using a cell proliferation assay, we demonstrated that conditioned media (CM) obtained from MSCs significantly enhanced the cell survival ability of fibroblast cells. Moreover, by measurement of mRNA and protein, we observed that CM also promoted the production or secretion of collagen, elastin, and fibronectin. To better understand the effects of ECM‐related wound healing, we measured the level of collagen‐degradative enzyme (matrix metalloprotease‐1), and observed that CM suppressed matrix metalloprotease‐1 expression. For the determination of oxidative stress, which has an influence on wound healing, we performed the superoxide dismutase and glutathione peroxidase assays; our results suggested that CM inhibited the oxidative stress of fibroblast cells. In order to widely investigate the wound‐healing effects of MSCs, we performed in vivo experiments, and observed that MSCs stimulated wound healing. In summary, the results of this study suggest that MSCs inhibit the loss of fibroblast cells and ECM, and accumulation of oxidative stress. We found that MSCs stimulate wound healing in vitro and in vivo, suggesting that MSCs have the potential to enhance wound healing.</abstract><cop>Malden, USA</cop><pub>Blackwell Publishing Inc</pub><pmid>20955344</pmid><doi>10.1111/j.1524-475X.2010.00636.x</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cell Movement Cell Proliferation Cell survival Collagen Collagen - metabolism Culture Media, Conditioned Dermis Elastin Elastin - metabolism Enzymes Epidermis Extracellular matrix Fibroblasts Fibroblasts - metabolism Fibronectin Fibronectins - metabolism Glutathione peroxidase Glutathione Peroxidase - metabolism Growth factors In Vitro Techniques Male Matrix Metalloproteinase 1 - metabolism Mesenchymal Stromal Cells - physiology Mesenchyme mRNA Oxidative Stress Rats Rats, Sprague-Dawley Secretion Skin Skin - cytology Skin - injuries Stem cells Superoxide dismutase Superoxide Dismutase - metabolism Wound Healing |
title | Mesenchymal stem cells' interaction with skin: Wound-healing effect on fibroblast cells and skin tissue |
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