Pre-treatments enhance the therapeutic effects of mesenchymal stem cells in liver diseases

被引:66
作者
Hu, Chenxia [1 ,2 ]
Wu, Zhongwen [1 ,2 ]
Li, Lanjuan [1 ,2 ]
机构
[1] Zhejiang Univ, Collaborat Innovat Ctr Diag & Treatment Infect Di, State Key Lab Diag & Treatment Infect Dis, Sch Med,Affiliated Hosp 1, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Univ, Affiliated Hosp 1, Natl Clin Res Ctr Infect Dis, Sch Med, Hangzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
gene modification; liver disease; mesenchymal stem cell; pre-treatment; survival; HEPATOCYTE-LIKE CELLS; HEPATIC DIFFERENTIATION; RAT MODEL; MICRORNA BIOGENESIS; IN-VITRO; TRANSPLANTATION; OVEREXPRESSION; TISSUE; IMMUNOMODULATION; PROLIFERATION;
D O I
10.1111/jcmm.14788
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Liver diseases caused by viral infection, alcohol abuse and metabolic disorders can progress to end-stage liver failure, liver cirrhosis and liver cancer, which are a growing cause of death worldwide. Although liver transplantation and hepatocyte transplantation are useful strategies to promote liver regeneration, they are limited by scarce sources of organs and hepatocytes. Mesenchymal stem cells (MSCs) restore liver injury after hepatogenic differentiation and exert immunomodulatory, anti-inflammatory, antifibrotic, antioxidative stress and antiapoptotic effects on liver cells in vivo. After isolation and culture in vitro, MSCs are faced with nutrient and oxygen deprivation, and external growth factors maintain MSC capacities for further applications. In addition, MSCs are placed in a harsh microenvironment, and anoikis and inflammation after transplantation in vivo significantly decrease their regenerative capacity. Pre-treatment with chemical agents, hypoxia, an inflammatory microenvironment and gene modification can protect MSCs against injury, and pre-treated MSCs show improved hepatogenic differentiation, homing capacity, survival and paracrine effects in vitro and in vivo in regard to attenuating liver injury. In this review, we mainly focus on pre-treatments and the underlying mechanisms for improving the therapeutic effects of MSCs in various liver diseases. Thus, we provide evidence for the development of MSC-based cell therapy to prevent acute or chronic liver injury. Mesenchymal stem cells have potential as a therapeutic to prolong the survival of patients with end-stage liver diseases in the near future.
引用
收藏
页码:40 / 49
页数:10
相关论文
共 76 条
[11]   The combination of miR-122 overexpression and Let-7f silencing induces hepatic differentiation of adipose tissue-derived stem cells [J].
Davoodian, Nahid ;
Lotfi, Abbas S. ;
Soleimani, Masoud ;
Ghaneialvar, Hori .
CELL BIOLOGY INTERNATIONAL, 2017, 41 (10) :1083-1092
[12]   MicroRNA-122 Overexpression Promotes Hepatic Differentiation of Human Adipose Tissue-Derived Stem Cells [J].
Davoodian, Nahid ;
Lotfi, Abbas S. ;
Soleimani, Masoud ;
Mowla, Seyed Javad .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2014, 115 (09) :1582-1593
[13]   Cytokine treatment optimises the immunotherapeutic effects of umbilical cord-derived MSC for treatment of inflammatory liver disease [J].
de Witte, Samantha F. H. ;
Merino, Ana M. ;
Franquesa, Marcella ;
Strini, Tanja ;
van Zoggel, Johanna A. A. ;
Korevaar, Sander S. ;
Luk, Franka ;
Gargesha, Madhu ;
O'Flynn, Lisa ;
Roy, Debashish ;
Elliman, Steve J. ;
Newsome, Philip N. ;
Baan, Carla C. ;
Hoogduijn, Martin J. .
STEM CELL RESEARCH & THERAPY, 2017, 8
[14]   Human hepatocyte transplantation: current experience and future challenges [J].
Dhawan, Anil ;
Puppi, Juliana ;
Hughes, Robin D. ;
Mitry, Ragai R. .
NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2010, 7 (05) :288-298
[15]   Overexpression of transcription factor Foxa2 and Hnf1α induced rat bone mesenchymal stem cells into hepatocytes [J].
Ding, Yi ;
Chang, Cuifang ;
Niu, Zhipeng ;
Dai, Keqiang ;
Geng, Xiaofang ;
Li, Deming ;
Guo, Jianlin ;
Xu, Cunshuan .
CYTOTECHNOLOGY, 2016, 68 (05) :2037-2047
[16]   The mesenchymal stem cell secretome as an acellular regenerative therapy for liver disease [J].
Driscoll, Julia ;
Patel, Tushar .
JOURNAL OF GASTROENTEROLOGY, 2019, 54 (09) :763-773
[17]   Intravenous Anesthetics Enhance the Ability of Human Bone Marrow-Derived Mesenchymal Stem Cells to Alleviate Hepatic Ischemia-Reperfusion Injury in a Receptor-Dependent Manner [J].
Feng, Jiayu ;
Yao, Weifeng ;
Zhang, Yihan ;
Xiang, Andy Peng ;
Yuan, Dongdong ;
Hei, Ziqing .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2018, 47 (02) :556-566
[18]  
Fisher L R, 1995, Liver Transpl Surg, V1, P10, DOI 10.1002/lt.500010104
[19]   Targeting MET in cancer: rationale and progress [J].
Gherardi, Ermanno ;
Birchmeier, Walter ;
Birchmeier, Carmen ;
Woude, George Vande .
NATURE REVIEWS CANCER, 2012, 12 (02) :89-103
[20]  
Gregory RI, 2005, CELL, V123, P631, DOI 10.1016/j.cell.2005.10.022