Extracellular Vesicles as Drivers of Non-Alcoholic Fatty Liver Disease: Small Particles with Big Impact

被引:17
作者
Ipsen, David Hojland [1 ]
Tveden-Nyborg, Pernille [1 ]
机构
[1] Univ Copenhagen, Sect Expt Anim Model, Dept Vet & Anim Sci, Ridebanevej 9, DK-1870 Frederiksberg, Denmark
关键词
nonalcoholic fatty liver disease; nonalcoholic steatohepatitis; extracellular vesicles;
D O I
10.3390/biomedicines9010093
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nonalcoholic fatty liver disease (NAFLD) is becoming the leading chronic liver disease, negatively affecting the lives of millions of patients worldwide. The complex pathogenesis involves crosstalk between multiple cellular networks, but how the intricate communication between these cells drives disease progression remains to be further elucidated. Furthermore, the disease is not limited to the liver and includes the reprogramming of distant cell populations in different organs. Extracellular vesicles (EVs) have gained increased attention as mediators of cellular communication. EVs carry specific cargos that can act as disease-specific signals both locally and systemically. Focusing on NAFLD advancing to steatohepatitis (NASH), this review provides an update on current experimental and clinical findings of the potential role of EVs in hepatic inflammation and fibrosis, the main contributors to progressive NASH. Particular attention is placed on the characteristics of EV cargos and potential specificity to disease stages, with putative value as disease markers and treatment targets for future investigations.
引用
收藏
页码:1 / 13
页数:13
相关论文
共 70 条
[1]   Non-alcoholic fatty liver disease and its relationship with cardiovascular disease and other extrahepatic diseases [J].
Adams, Leon A. ;
Anstee, Quentin M. ;
Tilg, Herbert ;
Targher, Giovanni .
GUT, 2017, 66 (06) :1138-1153
[2]   An Open-Label, Dose-Escalation Study to Assess the Safety and Efficacy of IL-22 Agonist F-652 in Patients With Alcohol-associated Hepatitis [J].
Arab, Juan P. ;
Sehrawat, Tejasav S. ;
Simonetto, Douglas A. ;
Verma, Vikas K. ;
Feng, Dechun ;
Tang, Tom ;
Dreyer, Kevin ;
Yan, Xiaoqiang ;
Daley, William L. ;
Sanyal, Arun ;
Chalasani, Naga ;
Radaeva, Svetlana ;
Yang, Liu ;
Vargas, Hugo ;
Ibacache, Mauricio ;
Gao, Bin ;
Gores, Gregory J. ;
Malhi, Harmeet ;
Kamath, Patrick S. ;
Shah, Vijay H. .
HEPATOLOGY, 2020, 72 (02) :441-453
[3]   Nonalcoholic fatty liver disease is associated with an almost twofold increased risk of incident type 2 diabetes and metabolic syndrome. Evidence from a systematic review and meta-analysis [J].
Ballestri, Stefano ;
Zona, Stefano ;
Targher, Giovanni ;
Romagnoli, Dante ;
Baldelli, Enrica ;
Nascimbeni, Fabio ;
Roverato, Alberto ;
Guaraldi, Giovanni ;
Lonardo, Amedeo .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2016, 31 (05) :936-944
[4]   Histological Assessment of NAFLD [J].
Bedossa, Pierre .
DIGESTIVE DISEASES AND SCIENCES, 2016, 61 (05) :1348-1355
[5]   Microvesicles released from fat-laden cells promote activation of hepatocellular NLRP3 inflammasome: A pro-inflammatory link between lipotoxicity and non-alcoholic steatohepatitis [J].
Cannito, Stefania ;
Morello, Elisabetta ;
Bocca, Claudia ;
Foglia, Beatrice ;
Benetti, Elisa ;
Novo, Erica ;
Chiazza, Fausto ;
Rogazzo, Mara ;
Fantozzi, Roberto ;
Povero, Davide ;
Sutti, Salvatore ;
Bugianesi, Elisabetta ;
Feldstein, Ariel E. ;
Albano, Emanuele ;
Collino, Massimo ;
Parola, Maurizio .
PLOS ONE, 2017, 12 (03)
[6]   Death Receptor 5 Signaling Promotes Hepatocyte Lipoapoptosis [J].
Cazanave, Sophie C. ;
Mott, Justin L. ;
Bronk, Steven F. ;
Werneburg, Nathan W. ;
Fingas, Christian D. ;
Meng, X. Wei ;
Finnberg, Niklas ;
El-Deiry, Wafik S. ;
Kaufmann, Scott H. ;
Gores, Gregory J. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (45) :39336-39348
[7]   Circulating MicroRNAs in Patients with Chronic Hepatitis C and Non-Alcoholic Fatty Liver Disease [J].
Cermelli, Silvia ;
Ruggieri, Anna ;
Marrero, Jorge A. ;
Ioannou, George N. ;
Beretta, Laura .
PLOS ONE, 2011, 6 (08)
[8]   Fibrogenic Signaling Is Suppressed in Hepatic Stellate Cells through Targeting of Connective Tissue Growth Factor (CCN2) by Cellular or Exosomal MicroRNA-199a-5p [J].
Chen, Li ;
Chen, Ruju ;
Velazquez, Victoria M. ;
Brigstock, David R. .
AMERICAN JOURNAL OF PATHOLOGY, 2016, 186 (11) :2921-2933
[9]   Suppression of fibrogenic signaling in hepatic stellate cells by Twist1-dependent microRNA-214 expression: Role of exosomes in horizontal transfer of Twist1 [J].
Chen, Li ;
Chen, Ruju ;
Kemper, Sherri ;
Charrier, Alyssa ;
Brigstock, David R. .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2015, 309 (06) :G491-G499
[10]   Epigenetic Regulation of Connective Tissue Growth Factor by MicroRNA-214 Delivery in Exosomes From Mouse or Human Hepatic Stellate Cells [J].
Chen, Li ;
Charrier, Alyssa ;
Zhou, Yu ;
Chen, Ruju ;
Yu, Bo ;
Agarwal, Kitty ;
Tsukamoto, Hidekazu ;
Lee, L. James ;
Paulaitis, Michael E. ;
Brigstock, David R. .
HEPATOLOGY, 2014, 59 (03) :1118-1129