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Conditioned Medium from Human Adipose-Derived Mesenchymal Stem Cell Culture Prevents UVB-Induced Skin Aging in Human Keratinocytes and Dermal Fibroblasts
Human adipose-derived mesenchymal stem cells-conditioned medium (ADSC-CM) contains cytokines and growth factors that can facilitate the regeneration and repair of various tissues and organs. In the present study, the protective activity of ADSC-CM treatment was investigated in UVB-irradiated human k...
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Published in: | International journal of molecular sciences 2019-12, Vol.21 (1), p.49 |
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description | Human adipose-derived mesenchymal stem cells-conditioned medium (ADSC-CM) contains cytokines and growth factors that can facilitate the regeneration and repair of various tissues and organs. In the present study, the protective activity of ADSC-CM treatment was investigated in UVB-irradiated human keratinocyte cell line HaCaTs and normal human dermal fibroblasts (NHDFs). It was found that ADSC-CM can modulate the expression of the signaling molecules in the early UVB responsive signaling pathways, including mitogen activated protein kinases (MAPKs), activator protein 1 (AP-1), and nuclear factor kappa B (NF-κB). In addition, ADSC-CM treatment could upregulate antioxidant response element (ARE) such as phase II gene heme oxygenase-1 (HO-1) and increase the expression of collagen synthesis enhancer gene transforming growth factor-β (TGF-β). The expression of matrix metalloproteinase-1 (MMP-1) and procollagen type I synthesis inhibitors such as interleukin-6 (IL-6) was also found to be suppressed upon ADSC-CM treatment. Taken together, our study illustrates the anti-photoaging activities of ADSC-CM in cell-based models. |
doi_str_mv | 10.3390/ijms21010049 |
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In the present study, the protective activity of ADSC-CM treatment was investigated in UVB-irradiated human keratinocyte cell line HaCaTs and normal human dermal fibroblasts (NHDFs). It was found that ADSC-CM can modulate the expression of the signaling molecules in the early UVB responsive signaling pathways, including mitogen activated protein kinases (MAPKs), activator protein 1 (AP-1), and nuclear factor kappa B (NF-κB). In addition, ADSC-CM treatment could upregulate antioxidant response element (ARE) such as phase II gene heme oxygenase-1 (HO-1) and increase the expression of collagen synthesis enhancer gene transforming growth factor-β (TGF-β). The expression of matrix metalloproteinase-1 (MMP-1) and procollagen type I synthesis inhibitors such as interleukin-6 (IL-6) was also found to be suppressed upon ADSC-CM treatment. Taken together, our study illustrates the anti-photoaging activities of ADSC-CM in cell-based models.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms21010049</identifier><identifier>PMID: 31861704</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Activator protein 1 ; Adipose Tissue - cytology ; Adipose Tissue - metabolism ; Aging ; Aging (artificial) ; Antioxidants ; Apoptosis ; Binding sites ; Cell culture ; Cell Culture Techniques ; Cells, Cultured ; Collagen ; Culture Media, Conditioned - pharmacology ; Cytokines - metabolism ; Fibroblasts ; Fibroblasts - cytology ; Fibroblasts - drug effects ; Fibroblasts - radiation effects ; Gene Expression Regulation - drug effects ; Gene Expression Regulation - radiation effects ; Growth factors ; Heme ; Heme oxygenase (decyclizing) ; Humans ; Interleukin 6 ; Interstitial collagenase ; Keratinocytes ; Keratinocytes - cytology ; Keratinocytes - drug effects ; Keratinocytes - radiation effects ; Kinases ; Matrix metalloproteinase ; Matrix Metalloproteinase 1 - metabolism ; Matrix metalloproteinases ; Mesenchymal stem cells ; Mesenchymal Stem Cells - cytology ; Mesenchymal Stem Cells - metabolism ; Metalloproteinase ; NF-κB protein ; Organs ; Oxygenase ; Phosphorylation ; Procollagen ; Proteins ; Radiation ; Signal transduction ; Signal Transduction - drug effects ; Signal Transduction - radiation effects ; Skin Aging - drug effects ; Stem cells ; Transcription factors ; Transforming growth factor-b ; Ultraviolet Rays - adverse effects ; Wound healing</subject><ispartof>International journal of molecular sciences, 2019-12, Vol.21 (1), p.49</ispartof><rights>2019 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/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 by the authors. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-d39caa9cefc17b72ae588d37af930c4eaddacb4f9172cd4c903c7f7c614ffb843</citedby><cites>FETCH-LOGICAL-c412t-d39caa9cefc17b72ae588d37af930c4eaddacb4f9172cd4c903c7f7c614ffb843</cites><orcidid>0000-0001-9369-6542 ; 0000-0001-5948-9929 ; 0000-0001-9787-465X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2548713204/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2548713204?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31861704$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Lu</creatorcontrib><creatorcontrib>Ngo, Hien T T</creatorcontrib><creatorcontrib>Hwang, Eunson</creatorcontrib><creatorcontrib>Wei, Xuan</creatorcontrib><creatorcontrib>Liu, Ying</creatorcontrib><creatorcontrib>Liu, Jia</creatorcontrib><creatorcontrib>Yi, Tae-Hoo</creatorcontrib><title>Conditioned Medium from Human Adipose-Derived Mesenchymal Stem Cell Culture Prevents UVB-Induced Skin Aging in Human Keratinocytes and Dermal Fibroblasts</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Human adipose-derived mesenchymal stem cells-conditioned medium (ADSC-CM) contains cytokines and growth factors that can facilitate the regeneration and repair of various tissues and organs. In the present study, the protective activity of ADSC-CM treatment was investigated in UVB-irradiated human keratinocyte cell line HaCaTs and normal human dermal fibroblasts (NHDFs). It was found that ADSC-CM can modulate the expression of the signaling molecules in the early UVB responsive signaling pathways, including mitogen activated protein kinases (MAPKs), activator protein 1 (AP-1), and nuclear factor kappa B (NF-κB). In addition, ADSC-CM treatment could upregulate antioxidant response element (ARE) such as phase II gene heme oxygenase-1 (HO-1) and increase the expression of collagen synthesis enhancer gene transforming growth factor-β (TGF-β). The expression of matrix metalloproteinase-1 (MMP-1) and procollagen type I synthesis inhibitors such as interleukin-6 (IL-6) was also found to be suppressed upon ADSC-CM treatment. Taken together, our study illustrates the anti-photoaging activities of ADSC-CM in cell-based models.</description><subject>Activator protein 1</subject><subject>Adipose Tissue - cytology</subject><subject>Adipose Tissue - metabolism</subject><subject>Aging</subject><subject>Aging (artificial)</subject><subject>Antioxidants</subject><subject>Apoptosis</subject><subject>Binding sites</subject><subject>Cell culture</subject><subject>Cell Culture Techniques</subject><subject>Cells, Cultured</subject><subject>Collagen</subject><subject>Culture Media, Conditioned - pharmacology</subject><subject>Cytokines - metabolism</subject><subject>Fibroblasts</subject><subject>Fibroblasts - cytology</subject><subject>Fibroblasts - drug effects</subject><subject>Fibroblasts - radiation effects</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Gene Expression Regulation - radiation effects</subject><subject>Growth factors</subject><subject>Heme</subject><subject>Heme oxygenase (decyclizing)</subject><subject>Humans</subject><subject>Interleukin 6</subject><subject>Interstitial collagenase</subject><subject>Keratinocytes</subject><subject>Keratinocytes - cytology</subject><subject>Keratinocytes - drug effects</subject><subject>Keratinocytes - radiation effects</subject><subject>Kinases</subject><subject>Matrix metalloproteinase</subject><subject>Matrix Metalloproteinase 1 - metabolism</subject><subject>Matrix metalloproteinases</subject><subject>Mesenchymal stem cells</subject><subject>Mesenchymal Stem Cells - cytology</subject><subject>Mesenchymal Stem Cells - metabolism</subject><subject>Metalloproteinase</subject><subject>NF-κB protein</subject><subject>Organs</subject><subject>Oxygenase</subject><subject>Phosphorylation</subject><subject>Procollagen</subject><subject>Proteins</subject><subject>Radiation</subject><subject>Signal transduction</subject><subject>Signal Transduction - drug effects</subject><subject>Signal Transduction - radiation effects</subject><subject>Skin Aging - drug effects</subject><subject>Stem cells</subject><subject>Transcription factors</subject><subject>Transforming growth factor-b</subject><subject>Ultraviolet Rays - 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cytology</topic><topic>Adipose Tissue - metabolism</topic><topic>Aging</topic><topic>Aging (artificial)</topic><topic>Antioxidants</topic><topic>Apoptosis</topic><topic>Binding sites</topic><topic>Cell culture</topic><topic>Cell Culture Techniques</topic><topic>Cells, Cultured</topic><topic>Collagen</topic><topic>Culture Media, Conditioned - pharmacology</topic><topic>Cytokines - metabolism</topic><topic>Fibroblasts</topic><topic>Fibroblasts - cytology</topic><topic>Fibroblasts - drug effects</topic><topic>Fibroblasts - radiation effects</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Gene Expression Regulation - radiation effects</topic><topic>Growth factors</topic><topic>Heme</topic><topic>Heme oxygenase (decyclizing)</topic><topic>Humans</topic><topic>Interleukin 6</topic><topic>Interstitial collagenase</topic><topic>Keratinocytes</topic><topic>Keratinocytes - cytology</topic><topic>Keratinocytes - drug effects</topic><topic>Keratinocytes - radiation effects</topic><topic>Kinases</topic><topic>Matrix metalloproteinase</topic><topic>Matrix Metalloproteinase 1 - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Lu</au><au>Ngo, Hien T T</au><au>Hwang, Eunson</au><au>Wei, Xuan</au><au>Liu, Ying</au><au>Liu, Jia</au><au>Yi, Tae-Hoo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Conditioned Medium from Human Adipose-Derived Mesenchymal Stem Cell Culture Prevents UVB-Induced Skin Aging in Human Keratinocytes and Dermal Fibroblasts</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2019-12-19</date><risdate>2019</risdate><volume>21</volume><issue>1</issue><spage>49</spage><pages>49-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Human adipose-derived mesenchymal stem cells-conditioned medium (ADSC-CM) contains cytokines and growth factors that can facilitate the regeneration and repair of various tissues and organs. In the present study, the protective activity of ADSC-CM treatment was investigated in UVB-irradiated human keratinocyte cell line HaCaTs and normal human dermal fibroblasts (NHDFs). It was found that ADSC-CM can modulate the expression of the signaling molecules in the early UVB responsive signaling pathways, including mitogen activated protein kinases (MAPKs), activator protein 1 (AP-1), and nuclear factor kappa B (NF-κB). In addition, ADSC-CM treatment could upregulate antioxidant response element (ARE) such as phase II gene heme oxygenase-1 (HO-1) and increase the expression of collagen synthesis enhancer gene transforming growth factor-β (TGF-β). The expression of matrix metalloproteinase-1 (MMP-1) and procollagen type I synthesis inhibitors such as interleukin-6 (IL-6) was also found to be suppressed upon ADSC-CM treatment. Taken together, our study illustrates the anti-photoaging activities of ADSC-CM in cell-based models.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>31861704</pmid><doi>10.3390/ijms21010049</doi><orcidid>https://orcid.org/0000-0001-9369-6542</orcidid><orcidid>https://orcid.org/0000-0001-5948-9929</orcidid><orcidid>https://orcid.org/0000-0001-9787-465X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Activator protein 1 Adipose Tissue - cytology Adipose Tissue - metabolism Aging Aging (artificial) Antioxidants Apoptosis Binding sites Cell culture Cell Culture Techniques Cells, Cultured Collagen Culture Media, Conditioned - pharmacology Cytokines - metabolism Fibroblasts Fibroblasts - cytology Fibroblasts - drug effects Fibroblasts - radiation effects Gene Expression Regulation - drug effects Gene Expression Regulation - radiation effects Growth factors Heme Heme oxygenase (decyclizing) Humans Interleukin 6 Interstitial collagenase Keratinocytes Keratinocytes - cytology Keratinocytes - drug effects Keratinocytes - radiation effects Kinases Matrix metalloproteinase Matrix Metalloproteinase 1 - metabolism Matrix metalloproteinases Mesenchymal stem cells Mesenchymal Stem Cells - cytology Mesenchymal Stem Cells - metabolism Metalloproteinase NF-κB protein Organs Oxygenase Phosphorylation Procollagen Proteins Radiation Signal transduction Signal Transduction - drug effects Signal Transduction - radiation effects Skin Aging - drug effects Stem cells Transcription factors Transforming growth factor-b Ultraviolet Rays - adverse effects Wound healing |
title | Conditioned Medium from Human Adipose-Derived Mesenchymal Stem Cell Culture Prevents UVB-Induced Skin Aging in Human Keratinocytes and Dermal Fibroblasts |
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