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Abstract

Liver regeneration is a complex process involving the crosstalk of multiple cell types, including hepatocytes, hepatic stellate cells, endothelial cells and inflammatory cells. The healthy liver is mitotically quiescent, but following toxic damage or resection the cells can rapidly enter the cell cycle to restore liver mass and function. During this process of regeneration, epithelial and non-parenchymal cells respond in a tightly coordinated fashion. Recent studies have described the interaction between inflammatory cells and a number of other cell types in the liver. In particular, macrophages can support biliary regeneration, contribute to fibrosis remodelling by repressing hepatic stellate cell activation and improve liver regeneration by scavenging dead or dying cells in situ. In this Review, we describe the mechanisms of tissue repair following damage, highlighting the close relationship between inflammation and liver regeneration, and discuss how recent findings can help design novel therapeutic approaches.

Liver regeneration involves multiple cell types, including hepatocytes, hepatic stellate cells, endothelial cells and inflammatory cells. Recent studies have elucidated the interactions between these cells during regeneration as well as the mechanisms that regulate cell proliferation and fibrosis remodelling, and have uncovered macrophages as key players. Such findings can help design novel therapeutic approaches.

Details

Title
Liver regeneration and inflammation: from fundamental science to clinical applications
Author
Campana, Lara 1   VIAFID ORCID Logo  ; Esser, Hannah 1 ; Huch Meritxell 2   VIAFID ORCID Logo  ; Forbes, Stuart 1   VIAFID ORCID Logo 

 Institute of Regeneration and Repair, The University of Edinburgh, Centre for Regenerative Medicine, Edinburgh, UK (GRID:grid.4305.2) (ISNI:0000 0004 1936 7988) 
 Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany (GRID:grid.419537.d) (ISNI:0000 0001 2113 4567) 
Pages
608-624
Publication year
2021
Publication date
Sep 2021
Publisher
Nature Publishing Group
ISSN
14710072
e-ISSN
14710080
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2562646411
Copyright
© Springer Nature Limited 2021.