Mesenchymal stem cells facilitate recovery from chemically induced liver damage and decrease liver fibrosis

被引:75
作者
Chang, Yao-Jen [3 ]
Liu, Jen-Wea [1 ,2 ]
Lin, Po-Cheng [1 ,2 ]
Sun, Li-Yi [1 ,2 ]
Peng, Chih-Wen [4 ,5 ]
Luo, Geng-Hong [1 ,2 ]
Chen, Tse-Min [6 ]
Lee, Ru-Ping [7 ]
Lin, Shinn-Zong [8 ,9 ,10 ,11 ]
Harn, Horng-Jyh [12 ,13 ]
Chiou, Tzyy-Wen [1 ,2 ]
机构
[1] Natl Dong Hwa Univ, Dept Life Sci, Shoufeng, Hualien, Taiwan
[2] Natl Dong Hwa Univ, Grad Inst Biotechnol, Shoufeng, Hualien, Taiwan
[3] Buddhist Tzu Chi Gen Hosp Taipei Branch, Dept Surg, Taipei, Taiwan
[4] Tzu Chi Univ & Hosp, Dept Life Sci, Hualien, Taiwan
[5] Tzu Chi Univ & Hosp, Gene Therapy Div, Hualien, Taiwan
[6] Hualien Armed Force Gen Hosp, Dept Lab, Hualien, Taiwan
[7] Tzu Chi Univ, Dept Nursery, Hualien, Taiwan
[8] China Med Univ & Hosp, Ctr Neuropsychiat, Taichung, Taiwan
[9] Beigang Hosp, Taichung, Taiwan
[10] Beigang Hosp, Yunlin, Taiwan
[11] China Med Univ & Hosp, Ctr Neuropsychiat, Yunlin, Taiwan
[12] China Med Univ Hosp, Dept Pathol, Taichung, Taiwan
[13] China Med Univ, Dept Pathol, Taichung, Taiwan
关键词
Liver damage; Liver fibrosis; Metalloproteinase; Carbon tetrachloride; Bone marrow mesenchymal stem cell; Green fluorescent protein; HEPATOCYTE GROWTH-FACTOR; MATRIX METALLOPROTEINASE-13; DIFFERENTIATION; RAT; EXPRESSION; REGENERATION;
D O I
10.1016/j.lfs.2009.08.003
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Aims: To investigate the feasibility and mechanism of liver damage repair using human bone marrow mesenchymal stem cells (hBMMSCs), we investigated the potential for hBMMSCs in recovery from liver damage, including fibrotic liver repair, using the CCl4-induced model for liver damage in the rat. Main methods: Rats were injected with 0.5 ml/kg CCl4 to induce liver damage and progressive liver fibrosis. hBMMSCs labeled with GFP were injected into the rats through the portal vein. Key findings: After one day of transplantation, GFP-labeled cells were found around the liver lobules, the hepatic blood vessels, and the edge of the liver lobes. Biochemical and histopathological analyses showed significantly increased recovery from liver damage in the transplanted group. In addition, transplanted hBMMSCs express matrix metalloproteinases (MMP), and liver fibrosis was significantly decreased. The degree of fibrosis reduction paralleled the number of hBMMSCs observed in liver sections. Significance: Our data suggest that hBMMSCs may facilitate recovery from chronic liver damage and may decrease liver fibrosis. Therefore, hBMMSCs are a potential option for treatment of liver cirrhosis. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:517 / 525
页数:9
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