Sinusoidal endotheliopathy in nonalcoholic steatohepatitis: therapeutic implications

Liver sinusoidal endothelial cells (LSECs) are distinct subtypes of endothelial cells lining a low flow vascular bed at the interface of the Over parenchyma and the circulating immune cells and soluble factors. Emerging literature implicates LSEC in the pathogenesis and progression of nonalcoholic fatty liver disease (NAFLD). During the evolution of NAFLD, LSEC dysfunction ensues. LSECs undergo morphological and functional transformation known as capillarization, as well as a pathogenic increase in surface adhesion molecules expression, referred to in this review as endotheliopathy. LSECs govern the composition of hepatic immune cell populations in nonalcoholic steatohepatis (NASH) by mediating leukocyte subset adhesion through specific combinations of activated adhesion molecules and secreted chemokines. Moreover, extracellular vesicles released by hepatocyte under lipotoxic stress in NASH act as a catalyst for the inflammatory response and promote immune cell chemotaxis and adhesion. In the current review, we highlight leukocyte adhesion to LSEC as an initiating event in the sterile inflammatory response in NASH. We discuss preclinical studies targeting immune cells adhesion in NASH mouse models and potential therapeutic anti-inflammatory strategies for human NASH.

Automated summary

Liver sinusoidal endothelial cells (LSECs) play a crucial role in the pathogenesis and progression of nonalcoholic fatty liver disease (NAFLD) by undergoing capillarization and expressing adhesion molecules. They regulate hepatic immune cell populations by mediating leukocyte subset adhesion in NAFLD, highlighting their role in the inflammatory response.