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Adipose-derived mesenchymal stem cells inhibit activation of hepatic stellate cells in vitro and ameliorate rat liver fibrosis in vivo
Background/purpose Previous studies suggested that mesenchymal stem cells may ameliorate fibrogenesis through the inhibition of hepatic stellate cells (HSCs) activation. This study aimed to investigate whether adipose derived mesenchymal stem cells (ADSCs) could modulate the activation of HSCs and c...
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Published in: | Journal of the Formosan Medical Association 2015-02, Vol.114 (2), p.130-138 |
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container_title | Journal of the Formosan Medical Association |
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creator | Yu, Fuxiang Ji, Shiqiang Su, Longfeng Wan, Li Zhang, Shengchu Dai, Chunlei Wang, Yang Fu, Junhui Zhang, Qiyu |
description | Background/purpose Previous studies suggested that mesenchymal stem cells may ameliorate fibrogenesis through the inhibition of hepatic stellate cells (HSCs) activation. This study aimed to investigate whether adipose derived mesenchymal stem cells (ADSCs) could modulate the activation of HSCs and contribute to the recovery of liver fibrogenesis. Methods ADSCs and HSCs were isolated from Sprague-Dawley rats and co-cultured using a transwells insert. Cell proliferation, apoptosis and smooth muscle α-actin (α-SMA) expression in HSCs were examined. Rats were injected with CCl4 to induce liver fibrogenesis. After injection of ADSCs through portal vein, the rats were examined for pathological changes in the liver. α-SMA expression and hydroxyproline content in the liver and serum levels of collagen III and hyaluronic acid was detected. Results After co-culturing for 72 h, the proliferation and activation of HSCs was inhibited by ADSCs and the apoptosis of HSCs was promoted by ADSCs. Transplantation of ADSCs inhibited liver fibrogenesis in the rats. Conclusion ADSCs inhibit the proliferation and activation of HSCs in vitro and inhibit liver fibrogenesis in rat model, suggesting the potential application of ADSCs in liver fibrogenesis therapy. |
doi_str_mv | 10.1016/j.jfma.2012.12.002 |
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fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_3534994fd56448f984345d2de4159bad</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S0929664612005840</els_id><doaj_id>oai_doaj_org_article_3534994fd56448f984345d2de4159bad</doaj_id><sourcerecordid>1655520518</sourcerecordid><originalsourceid>FETCH-LOGICAL-c521t-97cc1b857cd466ba52ab07c02e3402176b715eb9618f54c322c4ac64484bd94d3</originalsourceid><addsrcrecordid>eNp9UkuO1DAQzQLEDAMXYIG8ZNON7dhOLCGk0YjPSCOxANaWPxXawYkbOx2pb8AxOAsnw6ZnesECqWSX7PdeqepV07wgeEswEa_H7ThMeksxodsSGNNHzSWWVG6EYOKieZrziDETUoonzQXloutJxy-bn9fO72OGjYPkV3Boggyz3R0nHVBeYEIWQsjIzztv_IK0XfyqFx9nFAe0g33JbQWGoBc4g3__Wv2SItKzQ3qC4GOq3-VAoZRJaPAmxewfsGt81jwedMjw_P6-ar6-f_fl5uPm7tOH25vru43llCwb2VlLTM8765gQRnOqDe4sptAyTEknTEc4GClIP3BmW0ot01Yw1jPjJHPtVXN70nVRj2qf_KTTUUXt1d-HmL4pnUpPAVTLWyYlGxyv_EH2rGXcUQeMcGl01Xp10tqn-OMAeVGTz3UEeoZ4yIoIzjnFnPQFSk9QW9rOCYZzaYJVdVCNqjqoqoOqRHGwkF7e6x_MBO5MebCvAN6cAFAmtnpIKltf7APnE9iltOT_r__2H7oNfvZWh-9whDzGQ5qLF4qoXAjqc92nuk6EYsx7hts_ni_GgQ</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1655520518</pqid></control><display><type>article</type><title>Adipose-derived mesenchymal stem cells inhibit activation of hepatic stellate cells in vitro and ameliorate rat liver fibrosis in vivo</title><source>IngentaConnect Journals</source><creator>Yu, Fuxiang ; Ji, Shiqiang ; Su, Longfeng ; Wan, Li ; Zhang, Shengchu ; Dai, Chunlei ; Wang, Yang ; Fu, Junhui ; Zhang, Qiyu</creator><creatorcontrib>Yu, Fuxiang ; Ji, Shiqiang ; Su, Longfeng ; Wan, Li ; Zhang, Shengchu ; Dai, Chunlei ; Wang, Yang ; Fu, Junhui ; Zhang, Qiyu</creatorcontrib><description>Background/purpose Previous studies suggested that mesenchymal stem cells may ameliorate fibrogenesis through the inhibition of hepatic stellate cells (HSCs) activation. This study aimed to investigate whether adipose derived mesenchymal stem cells (ADSCs) could modulate the activation of HSCs and contribute to the recovery of liver fibrogenesis. Methods ADSCs and HSCs were isolated from Sprague-Dawley rats and co-cultured using a transwells insert. Cell proliferation, apoptosis and smooth muscle α-actin (α-SMA) expression in HSCs were examined. Rats were injected with CCl4 to induce liver fibrogenesis. After injection of ADSCs through portal vein, the rats were examined for pathological changes in the liver. α-SMA expression and hydroxyproline content in the liver and serum levels of collagen III and hyaluronic acid was detected. Results After co-culturing for 72 h, the proliferation and activation of HSCs was inhibited by ADSCs and the apoptosis of HSCs was promoted by ADSCs. Transplantation of ADSCs inhibited liver fibrogenesis in the rats. Conclusion ADSCs inhibit the proliferation and activation of HSCs in vitro and inhibit liver fibrogenesis in rat model, suggesting the potential application of ADSCs in liver fibrogenesis therapy.</description><identifier>ISSN: 0929-6646</identifier><identifier>DOI: 10.1016/j.jfma.2012.12.002</identifier><identifier>PMID: 25678175</identifier><language>eng</language><publisher>Singapore: Elsevier B.V</publisher><subject>Actins - metabolism ; adipose derived mesenchymal stem cells ; Adipose Tissue - cytology ; Animals ; Apoptosis ; Carbon Tetrachloride ; Cell Proliferation ; Cells, Cultured ; fibrosis ; hepatic stellate cells ; Hepatic Stellate Cells - cytology ; Internal Medicine ; Liver - pathology ; Liver Cirrhosis - chemically induced ; Liver Cirrhosis - therapy ; Male ; Mesenchymal Stem Cell Transplantation ; Mesenchymal Stromal Cells - cytology ; proliferation ; Rats ; Rats, Sprague-Dawley</subject><ispartof>Journal of the Formosan Medical Association, 2015-02, Vol.114 (2), p.130-138</ispartof><rights>2013</rights><rights>Copyright © 2013. Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c521t-97cc1b857cd466ba52ab07c02e3402176b715eb9618f54c322c4ac64484bd94d3</citedby><cites>FETCH-LOGICAL-c521t-97cc1b857cd466ba52ab07c02e3402176b715eb9618f54c322c4ac64484bd94d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25678175$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yu, Fuxiang</creatorcontrib><creatorcontrib>Ji, Shiqiang</creatorcontrib><creatorcontrib>Su, Longfeng</creatorcontrib><creatorcontrib>Wan, Li</creatorcontrib><creatorcontrib>Zhang, Shengchu</creatorcontrib><creatorcontrib>Dai, Chunlei</creatorcontrib><creatorcontrib>Wang, Yang</creatorcontrib><creatorcontrib>Fu, Junhui</creatorcontrib><creatorcontrib>Zhang, Qiyu</creatorcontrib><title>Adipose-derived mesenchymal stem cells inhibit activation of hepatic stellate cells in vitro and ameliorate rat liver fibrosis in vivo</title><title>Journal of the Formosan Medical Association</title><addtitle>J Formos Med Assoc</addtitle><description>Background/purpose Previous studies suggested that mesenchymal stem cells may ameliorate fibrogenesis through the inhibition of hepatic stellate cells (HSCs) activation. This study aimed to investigate whether adipose derived mesenchymal stem cells (ADSCs) could modulate the activation of HSCs and contribute to the recovery of liver fibrogenesis. Methods ADSCs and HSCs were isolated from Sprague-Dawley rats and co-cultured using a transwells insert. Cell proliferation, apoptosis and smooth muscle α-actin (α-SMA) expression in HSCs were examined. Rats were injected with CCl4 to induce liver fibrogenesis. After injection of ADSCs through portal vein, the rats were examined for pathological changes in the liver. α-SMA expression and hydroxyproline content in the liver and serum levels of collagen III and hyaluronic acid was detected. Results After co-culturing for 72 h, the proliferation and activation of HSCs was inhibited by ADSCs and the apoptosis of HSCs was promoted by ADSCs. Transplantation of ADSCs inhibited liver fibrogenesis in the rats. Conclusion ADSCs inhibit the proliferation and activation of HSCs in vitro and inhibit liver fibrogenesis in rat model, suggesting the potential application of ADSCs in liver fibrogenesis therapy.</description><subject>Actins - metabolism</subject><subject>adipose derived mesenchymal stem cells</subject><subject>Adipose Tissue - cytology</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Carbon Tetrachloride</subject><subject>Cell Proliferation</subject><subject>Cells, Cultured</subject><subject>fibrosis</subject><subject>hepatic stellate cells</subject><subject>Hepatic Stellate Cells - cytology</subject><subject>Internal Medicine</subject><subject>Liver - pathology</subject><subject>Liver Cirrhosis - chemically induced</subject><subject>Liver Cirrhosis - therapy</subject><subject>Male</subject><subject>Mesenchymal Stem Cell Transplantation</subject><subject>Mesenchymal Stromal Cells - cytology</subject><subject>proliferation</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><issn>0929-6646</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9UkuO1DAQzQLEDAMXYIG8ZNON7dhOLCGk0YjPSCOxANaWPxXawYkbOx2pb8AxOAsnw6ZnesECqWSX7PdeqepV07wgeEswEa_H7ThMeksxodsSGNNHzSWWVG6EYOKieZrziDETUoonzQXloutJxy-bn9fO72OGjYPkV3Boggyz3R0nHVBeYEIWQsjIzztv_IK0XfyqFx9nFAe0g33JbQWGoBc4g3__Wv2SItKzQ3qC4GOq3-VAoZRJaPAmxewfsGt81jwedMjw_P6-ar6-f_fl5uPm7tOH25vru43llCwb2VlLTM8765gQRnOqDe4sptAyTEknTEc4GClIP3BmW0ot01Yw1jPjJHPtVXN70nVRj2qf_KTTUUXt1d-HmL4pnUpPAVTLWyYlGxyv_EH2rGXcUQeMcGl01Xp10tqn-OMAeVGTz3UEeoZ4yIoIzjnFnPQFSk9QW9rOCYZzaYJVdVCNqjqoqoOqRHGwkF7e6x_MBO5MebCvAN6cAFAmtnpIKltf7APnE9iltOT_r__2H7oNfvZWh-9whDzGQ5qLF4qoXAjqc92nuk6EYsx7hts_ni_GgQ</recordid><startdate>20150201</startdate><enddate>20150201</enddate><creator>Yu, Fuxiang</creator><creator>Ji, Shiqiang</creator><creator>Su, Longfeng</creator><creator>Wan, Li</creator><creator>Zhang, Shengchu</creator><creator>Dai, Chunlei</creator><creator>Wang, Yang</creator><creator>Fu, Junhui</creator><creator>Zhang, Qiyu</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><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>7X8</scope><scope>DOA</scope></search><sort><creationdate>20150201</creationdate><title>Adipose-derived mesenchymal stem cells inhibit activation of hepatic stellate cells in vitro and ameliorate rat liver fibrosis in vivo</title><author>Yu, Fuxiang ; Ji, Shiqiang ; Su, Longfeng ; Wan, Li ; Zhang, Shengchu ; Dai, Chunlei ; Wang, Yang ; Fu, Junhui ; Zhang, Qiyu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c521t-97cc1b857cd466ba52ab07c02e3402176b715eb9618f54c322c4ac64484bd94d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Actins - metabolism</topic><topic>adipose derived mesenchymal stem cells</topic><topic>Adipose Tissue - cytology</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Carbon Tetrachloride</topic><topic>Cell Proliferation</topic><topic>Cells, Cultured</topic><topic>fibrosis</topic><topic>hepatic stellate cells</topic><topic>Hepatic Stellate Cells - cytology</topic><topic>Internal Medicine</topic><topic>Liver - pathology</topic><topic>Liver Cirrhosis - chemically induced</topic><topic>Liver Cirrhosis - therapy</topic><topic>Male</topic><topic>Mesenchymal Stem Cell Transplantation</topic><topic>Mesenchymal Stromal Cells - cytology</topic><topic>proliferation</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yu, Fuxiang</creatorcontrib><creatorcontrib>Ji, Shiqiang</creatorcontrib><creatorcontrib>Su, Longfeng</creatorcontrib><creatorcontrib>Wan, Li</creatorcontrib><creatorcontrib>Zhang, Shengchu</creatorcontrib><creatorcontrib>Dai, Chunlei</creatorcontrib><creatorcontrib>Wang, Yang</creatorcontrib><creatorcontrib>Fu, Junhui</creatorcontrib><creatorcontrib>Zhang, Qiyu</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of the Formosan Medical Association</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yu, Fuxiang</au><au>Ji, Shiqiang</au><au>Su, Longfeng</au><au>Wan, Li</au><au>Zhang, Shengchu</au><au>Dai, Chunlei</au><au>Wang, Yang</au><au>Fu, Junhui</au><au>Zhang, Qiyu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adipose-derived mesenchymal stem cells inhibit activation of hepatic stellate cells in vitro and ameliorate rat liver fibrosis in vivo</atitle><jtitle>Journal of the Formosan Medical Association</jtitle><addtitle>J Formos Med Assoc</addtitle><date>2015-02-01</date><risdate>2015</risdate><volume>114</volume><issue>2</issue><spage>130</spage><epage>138</epage><pages>130-138</pages><issn>0929-6646</issn><abstract>Background/purpose Previous studies suggested that mesenchymal stem cells may ameliorate fibrogenesis through the inhibition of hepatic stellate cells (HSCs) activation. This study aimed to investigate whether adipose derived mesenchymal stem cells (ADSCs) could modulate the activation of HSCs and contribute to the recovery of liver fibrogenesis. Methods ADSCs and HSCs were isolated from Sprague-Dawley rats and co-cultured using a transwells insert. Cell proliferation, apoptosis and smooth muscle α-actin (α-SMA) expression in HSCs were examined. Rats were injected with CCl4 to induce liver fibrogenesis. After injection of ADSCs through portal vein, the rats were examined for pathological changes in the liver. α-SMA expression and hydroxyproline content in the liver and serum levels of collagen III and hyaluronic acid was detected. Results After co-culturing for 72 h, the proliferation and activation of HSCs was inhibited by ADSCs and the apoptosis of HSCs was promoted by ADSCs. Transplantation of ADSCs inhibited liver fibrogenesis in the rats. Conclusion ADSCs inhibit the proliferation and activation of HSCs in vitro and inhibit liver fibrogenesis in rat model, suggesting the potential application of ADSCs in liver fibrogenesis therapy.</abstract><cop>Singapore</cop><pub>Elsevier B.V</pub><pmid>25678175</pmid><doi>10.1016/j.jfma.2012.12.002</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Actins - metabolism adipose derived mesenchymal stem cells Adipose Tissue - cytology Animals Apoptosis Carbon Tetrachloride Cell Proliferation Cells, Cultured fibrosis hepatic stellate cells Hepatic Stellate Cells - cytology Internal Medicine Liver - pathology Liver Cirrhosis - chemically induced Liver Cirrhosis - therapy Male Mesenchymal Stem Cell Transplantation Mesenchymal Stromal Cells - cytology proliferation Rats Rats, Sprague-Dawley |
title | Adipose-derived mesenchymal stem cells inhibit activation of hepatic stellate cells in vitro and ameliorate rat liver fibrosis in vivo |
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