TY - JOUR
T1 - Emerging roles of liver sinusoidal endothelial cells in nonalcoholic steatohepatitis
AU - Furuta, Kunimaro
AU - Guo, Qianqian
AU - Hirsova, Petra
AU - Ibrahim, Samar H.
N1 - Funding Information:
Funding: This work was supported by the National Institute of Diabetes And Digestive And Kidney Diseases of the National Institutes of Health under Award DK 122948 (to SHI), and the American Association of Study of liver Disease (AASLD) Foundation Bridge Award (to SHI), JSPS Overseas Fellowship Program (to KF), and the NIH Silvio O. Conte Digestive Diseases Research Core Centers P30 grant mechanism (DK084567). Support was also provided to P. Hirsova by the AASLD Pinnacle Research Award and the Pilot and Feasibility Award from the Mayo Clinic Center for Cell Signaling in Gastroenterology (NIDDK P30DK084567).
Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/11
Y1 - 2020/11
N2 - Nonalcoholic steatohepatitis (NASH) has become a growing public health problem worldwide, yet its pathophysiology remains unclear. Liver sinusoidal endothelial cells (LSEC) have unique morphology and function, and play a critical role in liver homeostasis. Emerging literature implicates LSEC in many pathological processes in the liver, including metabolic dysregulation, inflammation, angiogenesis, and carcinogenesis. In this review, we highlight the current knowledge of the role of LSEC in each of the progressive phases of NASH pathophysiology (steatosis, inflammation, fibrosis, and the development of hepatocellular carcinoma). We discuss processes that have important roles in NASH progression including the detrimental transformation of LSEC called “capillarization”, production of inflammatory and profibrogenic mediators by LSEC as well as LSEC-mediated angiogenesis. The current review has a special emphasis on LSEC adhesion molecules, and their key role in the inflammatory response in NASH. Moreover, we discuss the pathogenic role of extracellular vesicles and their bioactive cargos in liver intercellular communication, inflammation, and fibrosis. Finally, we highlight LSEC-adhesion molecules and derived bioactive product as potential therapeutic targets for human NASH.
AB - Nonalcoholic steatohepatitis (NASH) has become a growing public health problem worldwide, yet its pathophysiology remains unclear. Liver sinusoidal endothelial cells (LSEC) have unique morphology and function, and play a critical role in liver homeostasis. Emerging literature implicates LSEC in many pathological processes in the liver, including metabolic dysregulation, inflammation, angiogenesis, and carcinogenesis. In this review, we highlight the current knowledge of the role of LSEC in each of the progressive phases of NASH pathophysiology (steatosis, inflammation, fibrosis, and the development of hepatocellular carcinoma). We discuss processes that have important roles in NASH progression including the detrimental transformation of LSEC called “capillarization”, production of inflammatory and profibrogenic mediators by LSEC as well as LSEC-mediated angiogenesis. The current review has a special emphasis on LSEC adhesion molecules, and their key role in the inflammatory response in NASH. Moreover, we discuss the pathogenic role of extracellular vesicles and their bioactive cargos in liver intercellular communication, inflammation, and fibrosis. Finally, we highlight LSEC-adhesion molecules and derived bioactive product as potential therapeutic targets for human NASH.
KW - Adhesion
KW - Angiogenesis
KW - Extracellular vesicles
KW - Fibrosis
KW - Inflammation
KW - Liver sinusoidal endothelial cells (LSEC)
KW - NASH
KW - Steatosis
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U2 - 10.3390/biology9110395
DO - 10.3390/biology9110395
M3 - Review article
AN - SCOPUS:85096075130
SN - 2079-7737
VL - 9
SP - 1
EP - 19
JO - Biology
JF - Biology
IS - 11
M1 - 395
ER -