TY - JOUR
T1 - Elucidating the metabolic regulation of liver regeneration
AU - Huang, Jiansheng
AU - Rudnick, David A.
N1 - Funding Information:
Supported by NIH grants DK-02900 and DK-068219 (D.A.R.), the American Digestive Health Foundation (Research Scholar Award), the Children’s Digestive Health and Nutrition Foundation (Investigator Development Award and Innovative Research Award), the Washington University Digestive Disease Research Core Center grant P30-DK52574 , March of Dimes (Basil O’Connor Award), and the Washington University and St. Louis Children’s Hospital Children’s Discovery Institute .
PY - 2014/2
Y1 - 2014/2
N2 - The regenerative capability of liver is well known, and the mechanisms that regulate liver regeneration are extensively studied. Such analyses have defined general principles that govern the hepatic regenerative response and implicated specific extracellular and intracellular signals as regulated during and essential for normal liver regeneration. Nevertheless, the most proximal events that stimulate liver regeneration and the distal signals that terminate this process remain incompletely understood. Recent data suggest that the metabolic response to hepatic insufficiency might be the proximal signal that initiates regenerative hepatocellular proliferation. This review provides an overview of the data in support of a metabolic model of liver regeneration and reflects on the clinical implications and areas for further study suggested by these findings.
AB - The regenerative capability of liver is well known, and the mechanisms that regulate liver regeneration are extensively studied. Such analyses have defined general principles that govern the hepatic regenerative response and implicated specific extracellular and intracellular signals as regulated during and essential for normal liver regeneration. Nevertheless, the most proximal events that stimulate liver regeneration and the distal signals that terminate this process remain incompletely understood. Recent data suggest that the metabolic response to hepatic insufficiency might be the proximal signal that initiates regenerative hepatocellular proliferation. This review provides an overview of the data in support of a metabolic model of liver regeneration and reflects on the clinical implications and areas for further study suggested by these findings.
UR - http://www.scopus.com/inward/record.url?scp=84892152491&partnerID=8YFLogxK
U2 - 10.1016/j.ajpath.2013.04.034
DO - 10.1016/j.ajpath.2013.04.034
M3 - Review article
C2 - 24139945
AN - SCOPUS:84892152491
SN - 0002-9440
VL - 184
SP - 309
EP - 321
JO - American Journal of Pathology
JF - American Journal of Pathology
IS - 2
ER -