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PMID: 8641555 Published · ppublish English Journal Article Review

Liver regeneration 3: Regulation of signal transduction during liver regeneration.

Diehl AM, Rai RM

Abstract

The liver has a tremendous capacity to regenerate. For example, after extensive hepatic resection, remaining hepatocytes proliferate to restore the mass of the organ within days to weeks. This proliferative response is fascinating because hepatocytes rarely replicate in the healthy adult liver. Instead, these cells perform highly specialized functions and exemplify mature, terminally differentiated cells. Therefore it is somewhat surprising that the liver can repopulate while performing its many obligate, organ-specific functions. Study of the regenerating liver remnant after partial hepatectomy has helped to delineate mechanisms that regulate proliferation and liver-specific functions in individual hepatocytes, as well as those that coordinate the behaviors of different liver cell populations to balance organ growth and tissue-specific gene expression. Hence, this review will focus on inter- and intracellular signals that regulate the hepatocyte phenotype after PH.

MeSH Terms
Animals Cell Division GTP-Binding Proteins/physiology Hepatectomy Humans Liver/cytology Liver Regeneration Receptor Protein-Tyrosine Kinases/physiology Signal Transduction
Chemicals
Receptor Protein-Tyrosine Kinases GTP-Binding Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Diehl A M
Gastrointestinal Division, Johns Hopkins University School of Medicine, Johns Hopkins University, Baltimore, Maryland 21205, USA.
Rai R M
Article Info
Journal
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Abbr.
FASEB J
ISSN
0892-6638
Published
1996-02-00
Pages
215-27
Language
English
Region
United States
NLM ID
8804484
Subset
IM
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