Hepatic Lipid Catabolism via PPARα-Lysosomal Crosstalk.
Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors which belong to the nuclear hormone receptor superfamily. They regulate key aspects of energy metabolism within cells. Recently, PPARα has been implicated in the regulation of autophagy-lysosomal function, which plays a key role in cellular energy metabolism. PPARα transcriptionally upregulates several genes involved in the autophagy-lysosomal degradative pathway that participates in lipolysis of triglycerides within the hepatocytes. Interestingly, a reciprocal regulation of PPARα nuclear action by autophagy-lysosomal activity also exists with implications in lipid metabolism. This review succinctly discusses the unique relationship between PPARα nuclear action and lysosomal activity and explores its impact on hepatic lipid homeostasis under pathological conditions such as non-alcoholic fatty liver disease (NAFLD).
Duke Scholars
Altmetric Attention Stats
Dimensions Citation Stats
Published In
DOI
EISSN
Publication Date
Volume
Issue
Location
Related Subject Headings
- Triglycerides
- Receptors, Cytoplasmic and Nuclear
- Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
- PPAR alpha
- Nuclear Receptor Co-Repressor 1
- Non-alcoholic Fatty Liver Disease
- Lysosomes
- Liver
- Lipolysis
- Humans
Citation
Published In
DOI
EISSN
Publication Date
Volume
Issue
Location
Related Subject Headings
- Triglycerides
- Receptors, Cytoplasmic and Nuclear
- Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha
- PPAR alpha
- Nuclear Receptor Co-Repressor 1
- Non-alcoholic Fatty Liver Disease
- Lysosomes
- Liver
- Lipolysis
- Humans