Hedgehog signaling maintains resident hepatic progenitors throughout life - PubMed (original) (raw)
. 2006 May;290(5):G859-70.
doi: 10.1152/ajpgi.00456.2005. Epub 2005 Dec 1.
Yin-Xiong Li, Alaa Melhem, Eva Schmelzer, Marzena Zdanowicz, Jiawen Huang, Montserrat Caballero, Jeff H Fair, John W Ludlow, Randall E McClelland, Lola M Reid, Anna Mae Diehl
Affiliations
- PMID: 16322088
- DOI: 10.1152/ajpgi.00456.2005
Free article
Hedgehog signaling maintains resident hepatic progenitors throughout life
Jason K Sicklick et al. Am J Physiol Gastrointest Liver Physiol. 2006 May.
Free article
Abstract
Hedgehog signaling through its receptor, Patched, activates transcription of genes, including Patched, that regulate the fate of various progenitors. Although Hedgehog signaling is required for endodermal commitment and hepatogenesis, the possibility that it regulates liver turnover in adults had not been considered because mature liver epithelial cells lack Hedgehog signaling. Herein, we show that this pathway is essential throughout life for maintaining hepatic progenitors. Patched-expressing cells have been identified among endodermally lineage-restricted, murine embryonic stem cells as well as in livers of fetal and adult Ptc-lacZ mice. An adult-derived, murine hepatic progenitor cell line expresses Patched, and Hedgehog-responsive cells exist in stem cell compartments of fetal and adult human livers. In both species, manipulation of Hedgehog activity influences hepatic progenitor cell survival. Therefore, Hedgehog signaling is conserved in hepatic progenitors from fetal development through adulthood and may be a new therapeutic target in patients with liver damage.
Publication types
MeSH terms
Substances
Grants and funding
- R01 AA 010154/AA/NIAAA NIH HHS/United States
- R01 AA 012059/AA/NIAAA NIH HHS/United States
- R01 AA 014243/AA/NIAAA NIH HHS/United States
- R01 DK 053792/DK/NIDDK NIH HHS/United States
- R01 DK 52851/DK/NIDDK NIH HHS/United States
- R01 IP30-DK-065933/DK/NIDDK NIH HHS/United States
- T32 DK 007713/DK/NIDDK NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases