The vascular endothelial growth factor signaling pathway regulates liver sinusoidal endothelial cells during liver regeneration after partial hepatectomy

Expert Rev Gastroenterol Hepatol. 2021 Feb;15(2):139-147. doi: 10.1080/17474124.2020.1815532. Epub 2020 Oct 14.

Abstract

Introduction: Liver regeneration after partial hepatectomy is a very complex and well-regulated procedure. It utilizes all liver cell types, which are associated with signaling pathways involving growth factors, cytokines, and stimulatory and inhibitory feedback of several growth-related signals. Liver sinusoidal endothelial cells (LSECs) contribute to liver regeneration after partial hepatectomy. Vascular endothelial growth factor (VEGF) has various functions in LSECs. In this review, we summarize the relationship between VEGF and LSECs involving VEGF regulatory activity in the vascular endothelium.

Areas covered: Maintenance of the fenestrated LSEC phenotype requires two VEGF pathways: VEGF stimulated-NO acting through the cGMP pathway and VEGF independent of nitric oxide (NO). The results suggest that VEGF is a key regenerating mediator of LSECs in the partial hepatectomy model. NO-independent pathway was also essential to the maintenance of the LSEC in liver regeneration.

Expert opinion: Liver regeneration remains a fascinating and significative research field in recent years. The liver involved of molecular pathways except for LSEC-VEGF pathways that make the field of liver further depth studies should be put into effect to elaborate the undetermined confusions, which will be better to understand liver regeneration.

Keywords: Liver regeneration; VEGF stimulated-NO pathway; fenestration; liver sinusoidal endothelial cells; partial hepatectomy; vascular endothelial growth factor.

Publication types

  • Review
  • Video-Audio Media

MeSH terms

  • Animals
  • Cell Proliferation
  • Endothelial Cells / metabolism*
  • Hepatectomy*
  • Hepatocytes / metabolism
  • Humans
  • Liver Regeneration / physiology*
  • Phenotype
  • Signal Transduction
  • Vascular Endothelial Growth Factors / metabolism*

Substances

  • Vascular Endothelial Growth Factors