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논문 기본 정보

자료유형
학술저널
저자정보
Wang Xianyao (Guizhou Medical University) Wang Huizhen (Nanyang Medical College) Lu Junhou (Medical College of Soochow University) Feng Zhanhui (Affiliated Hospital of Guizhou Medical University) Liu Zhongshan (Affiliated Hospital of Guizhou Medical University) Song Hailiang (Department of General Surgery Dalang Hospital) Wang Heng (Department of Pharmacology Qiannan Medical College for Nationalities) Zhou Yanhua (Guizhou Medical University) Xu Jianwei (School of Basic Medicine Guizhou Medical University)
저널정보
한국조직공학과 재생의학회 조직공학과 재생의학 조직공학과 재생의학 제17권 제5호
발행연도
2020.1
수록면
683 - 693 (11page)

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BACKGROUND: Mesenchymal stem cell (MSC)-based cell transplantation is an effective means of treating chronic liver injury, fibrosis and end-stage liver disease. However, extensive studies have found that only a small number of transplanted cells migrate to the site of injury or lesion, and repair efficacy is very limited. METHODS: Bone marrow-derived MSCs (BM-MSCs) were generated that overexpressed the erythropoietin (EPO) gene using a lentivirus. Cell Counting Kit-8 was used to detect the viability of BM-MSCs after overexpressing EPO. Cell migration and apoptosis were verified using Boyden chamber and flow cytometry, respectively. Finally, the anti-fibrosis efficacy of EPO-MSCs was evaluated in vivo using immunohistochemical analysis. RESULTS: EPO overexpression promoted cell viability and migration of BM-MSCs without inducing apoptosis, and EPO-MSC treatment significantly alleviated liver fibrosis in a carbon tetrachloride (CCl4) induced mouse liver fibrosis model. CONCLUSION: EPO-MSCs enhance anti-fibrotic efficacy, with higher cell viability and stronger migration ability compared with treatment with BM-MSCs only. These findings support improving the efficiency of MSCs transplantation as a potential therapeutic strategy for liver fibrosis.

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