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10.5966/sctm.2015-0265 http://scihub22266oqcxt.onion/10.5966/sctm.2015-0265 C5442725!5442725 !28170193     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=28170193 &cmd=llinks): Failed to open stream: HTTP request failed! 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Human Menstrual Blood-Derived Stem Cells Ameliorate Liver Fibrosis in Mice by Targeting Hepatic Stellate Cells via Paracrine Mediators |pdf=|usr=}}{{28170193 }} gab.com Text Human Menstrual Blood-Derived Stem Cells Ameliorate Liver Fibrosis in Mice by Targeting Hepatic Stellate Cells via Paracrine Mediators JO: Stem Cells Transl Med http://www.kidney.de/pget.php?&tw=1&pmid=28170193 #FOAvip Mesenchymal stem cells (MSCs) may have potential applications in regenerative medicine for the treatment of chronic liver diseases (CLDs). Human menstrual blood is a novel source of MSCs, termed menstrual blood-derived stem cells (MenSCs). Compared with bone marrow MSCs, MenSCs exhibit a higher proliferation rate and they can be obtained through a simple, safe, painless procedure without ethical concerns. Although the therapeutic efficacy of MenSCs has been explored in some diseases, their effects on liver fibrosis are still unclear. In the present study, we investigated the therapeutic effects of MenSC transplantation in a carbon tetrachloride-induced mouse model of liver fibrosis. These results revealed that MenSCs markedly improved liver function, attenuated collagen deposition, and inhibited activated hepatic stellate cells up to 2 weeks after transplantation. Moreover, tracking of green fluorescent protein-expressing MenSCs demonstrated that transplanted cells migrated to the sites of injury, but few differentiated into functional hepatocyte-like cells. Transwell coculturing experiments also showed that MenSCs suppressed proliferation of LX-2 cells (an immortalized hepatic stellate cell line) through secretion of monocyte chemoattractant protein-1, interleukin-6, hepatocyte growth factor, growth-related oncogene, interleukin-8, and osteoprotegerin. Collectively, our results provided preliminary evidence for the antifibrotic capacity of MenSCs in liver fibrosis and suggested that these cells may be an alternative therapeutic approach for the treatment of CLDs. Stem Cells Translational Medicine 2017;6:272-284. Twit Text FOAVip Human Menstrual Blood-Derived Stem Cells Ameliorate Liver Fibrosis in Mice by Targeting Hepatic Stellate Cells via Paracrine Mediators ????Stem Cells Transl Med http://www.kidney.de/pget.php?&tw=1&pmid=28170193 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28170193 #FOAvip English Wikipedia <ref>{{Cite pmid|28170193 }}</ref> Human Menstrual Blood-Derived Stem Cells Ameliorate Liver Fibrosis in Mice by Targeting Hepatic Stellate Cells via Paracrine Mediators #MMPMID28170193 Chen L ; Zhang C ; Chen L ; Wang X ; Xiang B ; Wu X ; Guo Y ; Mou X ; Yuan L ; Chen B ; Wang J ; Xiang C Stem Cells Transl Med 2017[Jan]; 6 (1 ): 272-284 PMID28170193 show ga Mesenchymal stem cells (MSCs) may have potential applications in regenerative medicine for the treatment of chronic liver diseases (CLDs). Human menstrual blood is a novel source of MSCs, termed menstrual blood-derived stem cells (MenSCs). Compared with bone marrow MSCs, MenSCs exhibit a higher proliferation rate and they can be obtained through a simple, safe, painless procedure without ethical concerns. Although the therapeutic efficacy of MenSCs has been explored in some diseases, their effects on liver fibrosis are still unclear. In the present study, we investigated the therapeutic effects of MenSC transplantation in a carbon tetrachloride-induced mouse model of liver fibrosis. These results revealed that MenSCs markedly improved liver function, attenuated collagen deposition, and inhibited activated hepatic stellate cells up to 2 weeks after transplantation. Moreover, tracking of green fluorescent protein-expressing MenSCs demonstrated that transplanted cells migrated to the sites of injury, but few differentiated into functional hepatocyte-like cells. Transwell coculturing experiments also showed that MenSCs suppressed proliferation of LX-2 cells (an immortalized hepatic stellate cell line) through secretion of monocyte chemoattractant protein-1, interleukin-6, hepatocyte growth factor, growth-related oncogene, interleukin-8, and osteoprotegerin. Collectively, our results provided preliminary evidence for the antifibrotic capacity of MenSCs in liver fibrosis and suggested that these cells may be an alternative therapeutic approach for the treatment of CLDs. Stem Cells Translational Medicine 2017;6:272-284. |*Menstruation [MESH] |*Paracrine Communication [MESH] |Actins/metabolism [MESH] |Animals [MESH] |Carbon Tetrachloride [MESH] |Cell Cycle Checkpoints [MESH] |Cell Movement [MESH] |Cell Proliferation [MESH] |Cell Shape [MESH] |Collagen/metabolism [MESH] |Cytokines/metabolism [MESH] |Gene Expression Regulation [MESH] |Hepatic Stellate Cells/*cytology [MESH] |Humans [MESH] |Immunophenotyping [MESH] |Liver Cirrhosis/genetics/pathology/*therapy [MESH] |Male [MESH] |Mice, Inbred ICR [MESH] |Stem Cell Transplantation [MESH] |Stem Cells/*cytology [MESH]Human Menstrual Blood-Derived Stem Cells Ameliorate Liver Fibrosis in (epmc).pdf DeepDyve Pubget Overpricing