TY - JOUR
T1 - Regulation of Liver Metabolism by Autophagy
AU - Madrigal-Matute, Julio
AU - Cuervo, Ana Maria
N1 - Funding Information:
The authors thank Drs Susmita Kaushik for critical reading of the manuscript. The authors apologize to those whose work could not be cited owing to space limitations. Supported by National Institutes of Health grants AG021904, AG031782, and DK098408, and the generous support of R&R Belfer (A.M.C.); and also supported by a postdoctoral fellowship from the American Diabetes Association Grant 1-15-MI-03 (J.M.M.).
Funding Information:
Funding Supported by National Institutes of Health grants AG021904 , AG031782 , and DK098408 , and the generous support of R&R Belfer (A.M.C.); and also supported by a postdoctoral fellowship from the American Diabetes Association Grant 1-15-MI-03 (J.M.M.).
Publisher Copyright:
© 2016 AGA Institute.
PY - 2016/2/1
Y1 - 2016/2/1
N2 - Intracellular components must be recycled for cells to maintain energy and ensure quality control of proteins and organelles. Autophagy is a highly conserved recycling process that involves degradation of cellular constituents in lysosomes. Although autophagy regulates a number of cell functions, it was first found to maintain energy balance in liver cells. As our understanding of autophagy has increased, we have found its connections to energy regulation in liver cells to be tight and complex. We review 3 mechanisms by which hepatic autophagy monitors and regulates cellular metabolism. Autophagy provides essential components (amino acids, lipids, and carbohydrates) required to meet the cell's energy needs, and it also regulates energy supply by controlling the number, quality, and dynamics of the mitochondria. Finally, autophagy also modulates levels of enzymes in metabolic pathways. In light of the multiple ways in which autophagy participates to control liver metabolism, it is no surprise that dysregulation of autophagy has been associated with metabolic diseases such as obesity, diabetes, or metabolic syndrome, as well as liver-specific disorders such as fatty liver, nonalcoholic steatohepatitis, and hepatocellular carcinoma. We discuss some of these connections and how hepatic autophagy might serve as a therapeutic target in common metabolic disorders.
AB - Intracellular components must be recycled for cells to maintain energy and ensure quality control of proteins and organelles. Autophagy is a highly conserved recycling process that involves degradation of cellular constituents in lysosomes. Although autophagy regulates a number of cell functions, it was first found to maintain energy balance in liver cells. As our understanding of autophagy has increased, we have found its connections to energy regulation in liver cells to be tight and complex. We review 3 mechanisms by which hepatic autophagy monitors and regulates cellular metabolism. Autophagy provides essential components (amino acids, lipids, and carbohydrates) required to meet the cell's energy needs, and it also regulates energy supply by controlling the number, quality, and dynamics of the mitochondria. Finally, autophagy also modulates levels of enzymes in metabolic pathways. In light of the multiple ways in which autophagy participates to control liver metabolism, it is no surprise that dysregulation of autophagy has been associated with metabolic diseases such as obesity, diabetes, or metabolic syndrome, as well as liver-specific disorders such as fatty liver, nonalcoholic steatohepatitis, and hepatocellular carcinoma. We discuss some of these connections and how hepatic autophagy might serve as a therapeutic target in common metabolic disorders.
KW - Cancer
KW - Chaperone-Mediated Autophagy
KW - Lipophagy
KW - Lysosome
KW - Macroautophagy
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U2 - 10.1053/j.gastro.2015.09.042
DO - 10.1053/j.gastro.2015.09.042
M3 - Review article
C2 - 26453774
AN - SCOPUS:84959470663
SN - 0016-5085
VL - 150
SP - 328
EP - 339
JO - Gastroenterology
JF - Gastroenterology
IS - 2
ER -