Recent advances in the role of exosomes in liver fibrosis

被引:7
作者
Shen, Jiliang [1 ]
Cao, Jiasheng [1 ]
Chen, Mingyu [1 ,4 ]
Zhang, Yaping [2 ,3 ]
机构
[1] Sir Run Run Shaw Hosp, Dept Gen Surg, Hangzhou, Peoples R China
[2] Zhejiang Univ, Sir Run Run Shaw Hosp, Sch Med, Dept Anesthesiol, Hangzhou, Peoples R China
[3] Zhejiang Univ, Sir Run Run Shaw Hosp, Sch Med, 3 East Qing Chun Rd, Hangzhou 310016, Zhejiang, Peoples R China
[4] Zhejiang Univ, Sir Run Run Shaw Hosp, Sch Med, Dept Gen Surg, Hangzhou 310016, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
exosome; hepatic stellate cell; liver fibrosis; mesenchymal stem cell; microRNA; vesicle; HEPATIC STELLATE CELLS; MESENCHYMAL STEM-CELLS; AUTOPHAGY;
D O I
10.1111/jgh.16203
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and AimWe aim to summarize the current status of research on the role of exosomes in liver fibrosis. MethodsA review of the relevant literature was performed and the key findings were presented. ResultsMost studies focused on the role of exosomes derived from mesenchymal stem cells, other types of stem cells, and liver resident cells including hepatocytes, cholangiocytes, and hepatic stellate cells in liver fibrosis. Exosomes have been reported to play an essential role in the inactivation or activation of hepatic stellate cells through the delivery of non-coding RNAs and proteins. In recent years, this exosome cargo has become a research hotspot. ConclusionsRecent studies have indicated the potential therapeutic benefit of exosomes in liver fibrosis.
引用
收藏
页码:1083 / 1088
页数:6
相关论文
共 39 条
[31]   Development of a novel anti-HER2 scFv by ribosome display and in silico evaluation of its 3D structure and interaction with HER2, alone and after fusion to LAMP2B [J].
Salimi, Fatemeh ;
Moghadam, Mehdi Forouzandeh ;
Rajabibazl, Masoumeh .
MOLECULAR BIOLOGY REPORTS, 2018, 45 (06) :2247-2256
[32]   H19 Promotes Cholestatic Liver Fibrosis by Preventing ZEB1-Mediated Inhibition of Epithelial Cell Adhesion Molecule [J].
Song, Yongfeng ;
Liu, Chune ;
Liu, Xia ;
Trottier, Jocelyn ;
Beaudoin, Michele ;
Zhang, Li ;
Pope, Chad ;
Peng, Guangyong ;
Barbier, Olivier ;
Zhong, Xiaobo ;
Li, Linheng ;
Wang, Li .
HEPATOLOGY, 2017, 66 (04) :1183-1196
[33]   A novel mouse model of depletion of stellate cells clarifies their role in ischemia/reperfusion- and endotoxin-induced acute liver injury [J].
Stewart, Rachel K. ;
Dangi, Anil ;
Huang, Chao ;
Murase, Noriko ;
Kimura, Shoko ;
Stolz, Donna B. ;
Wilson, Gregory C. ;
Lentsch, Alex B. ;
Gandhi, Chandrashekhar R. .
JOURNAL OF HEPATOLOGY, 2014, 60 (02) :298-305
[34]   Exosome-mediated delivery of Cas9 ribonucleoprotein complexes for tissue-specific gene therapy of liver diseases [J].
Wan, Tao ;
Zhong, Jiafeng ;
Pan, Qi ;
Zhou, Tianhua ;
Ping, Yuan ;
Liu, Xiangrui .
SCIENCE ADVANCES, 2022, 8 (37)
[35]   Exosomal miR-223 derived from natural killer cells inhibits hepatic stellate cell activation by suppressing autophagy [J].
Wang, Ling ;
Wang, Yinghao ;
Quan, Jun .
MOLECULAR MEDICINE, 2020, 26 (01)
[36]   Exosome Adherence and Internalization by Hepatic Stellate Cells Triggers Sphingosine 1-Phosphate-dependent Migration [J].
Wang, Ruisi ;
Ding, Qian ;
Yaqoob, Usman ;
de Assuncao, Thiago M. ;
Verma, Vikas K. ;
Hirsova, Petra ;
Cao, Sheng ;
Mukhopadhyay, Debabrata ;
Huebert, Robert C. ;
Shah, Vijay H. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2015, 290 (52) :30684-U51
[37]   In Vivo Genome-Wide CRISPR Activation Screening Identifies Functionally Important Long Noncoding RNAs in Hepatocellular Carcinoma [J].
Wong, Lok-Sze ;
Wei, Lai ;
Wang, Gengchao ;
Law, Cheuk-Ting ;
Tsang, Felice Ho-Ching ;
Chin, Wai-Ching ;
Ng, Irene Oi-Lin ;
Wong, Chun-Ming .
CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY, 2022, 14 (05) :1053-1076
[38]   hucMSC Exosome-Derived GPX1 Is Required for the Recovery of Hepatic Oxidant Injury [J].
Yan, Yongmin ;
Jiang, Wenqian ;
Tan, Youwen ;
Zou, Shengqiang ;
Zhang, Hongguang ;
Mao, Fei ;
Gong, Aihua ;
Qian, Hui ;
Xu, Wenrong .
MOLECULAR THERAPY, 2017, 25 (02) :465-479
[39]   Disrupting the TRIB3-SQSTM1 interaction reduces liver fibrosis by restoring autophagy and suppressing exosome-mediated HSC activation [J].
Zhang, Xiao-Wei ;
Zhou, Ji-Chao ;
Peng, Dian ;
Hua, Fang ;
Li, Ke ;
Yu, Jiao-Jiao ;
Lv, Xiao-Xi ;
Cui, Bing ;
Liu, Shan-Shan ;
Yu, Jin-Mei ;
Wang, Feng ;
Jin, Cai-Cai ;
Yang, Zhao-Na ;
Zhao, Chen-Xi ;
Hou, Xue-Ying ;
Huang, Bo ;
Hu, Zhuo-Wei .
AUTOPHAGY, 2020, 16 (05) :782-796