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Human umbilical cord/placenta mesenchymal stem cell conditioned medium attenuates intestinal fibrosis in vivo and in vitro

Authors
 Yoon Jeong Choi  ;  Woo Ram Kim  ;  Duk Hwan Kim  ;  Jee Hyun Kim  ;  Jun Hwan Yoo 
Citation
 STEM CELL RESEARCH & THERAPY, Vol.15(1) : 69, 2024-03 
Journal Title
STEM CELL RESEARCH & THERAPY
Issue Date
2024-03
MeSH
Actins / metabolism ; Animals ; Colitis* / chemically induced ; Colitis* / metabolism ; Colitis* / therapy ; Culture Media, Conditioned / metabolism ; Culture Media, Conditioned / pharmacology ; Dextran Sulfate / toxicity ; Disease Models, Animal ; Fibrosis ; Humans ; Immunologic Factors ; Mesenchymal Stem Cells* / metabolism ; Mice ; Mice, Inbred C57BL ; Transforming Growth Factor beta1 / metabolism ; Umbilical Cord
Keywords
Conditioned medium ; Intestinal fibrosis ; Mesenchymal stem cells ; Placenta ; Umbilical cord
Abstract
Background: A significant unmet need in inflammatory bowel disease is the lack of anti-fibrotic agents targeting intestinal fibrosis. This study aimed to investigate the anti-fibrogenic properties and mechanisms of the conditioned medium (CM) from human umbilical cord/placenta-derived mesenchymal stem cells (UC/PL-MSC-CM) in a murine intestinal fibrosis model and human primary intestinal myofibroblasts (HIMFs). Methods: UC/PL-MSC-CM was concentrated 15-fold using a 3 kDa cut-off filter. C57BL/6 mice aged 7 weeks old were randomly assigned to one of four groups: (1) control, (2) dextran sulfate sodium (DSS), (3) DSS + CM (late-phase treatment), and (4) DSS + CM (early-phase treatment). Chronic DSS colitis and intestinal fibrosis was induced by three cycles of DSS administration. One DSS cycle consisted of 7 days of oral DSS administration (1.75%, 2%, and 2.5% DSS), followed by 14 days of drinking water. UC/PL-MSC-CM was intraperitoneally administered in the late phase (from day 50, 10 times) or early phase (from day 29, 10 times) of DSS cycles. HIMFs were treated with TGF-β1 and co-treated with UC/PL-MSC-CM (10% of culture media) in the cellular model. Results: In the animal study, UC/PL-MSC-CM reduced submucosa/muscularis propria thickness and collagen deposition, which improved intestinal fibrosis in chronic DSS colitis. The UC/PL-MSC-CM significantly reduced the expressions of procollagen1A1 and α-smooth muscle actin, which DSS significantly elevated. The anti-fibrogenic effect was more apparent in the UC-MSC-CM or early-phase treatment model. The UC/PL-MSC-CM reduced procollagen1A1, fibronectin, and α-smooth muscle actin expression in HIMFs in the cellular model. The UC/PL-MSC-CM downregulated fibrogenesis by suppressing RhoA, MRTF-A, and SRF expression. Conclusions: Human UC/PL-MSC-CM inhibits TGF-β1-induced fibrogenic activation in HIMFs by blocking the Rho/MRTF/SRF pathway and chronic DSS colitis-induced intestinal fibrosis. Thus, it may be regarded as a novel candidate for stem cell-based therapy of intestinal fibrosis. © The Author(s) 2024.
Files in This Item:
T202404188.pdf Download
DOI
10.1186/s13287-024-03678-4
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Woo Ram(김우람)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/200093
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