Please use this identifier to cite or link to this item: https://doi.org/10.3390/ijms21072391
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dc.titleHepatic Lipid Catabolism via PPAR alpha-Lysosomal Crosstalk
dc.contributor.authorSinha, Rohit A
dc.contributor.authorRajak, Sangam
dc.contributor.authorSingh, Brijesh K
dc.contributor.authorYen, Paul M
dc.date.accessioned2022-06-08T06:14:25Z
dc.date.available2022-06-08T06:14:25Z
dc.date.issued2020-04-01
dc.identifier.citationSinha, Rohit A, Rajak, Sangam, Singh, Brijesh K, Yen, Paul M (2020-04-01). Hepatic Lipid Catabolism via PPAR alpha-Lysosomal Crosstalk. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 21 (7). ScholarBank@NUS Repository. https://doi.org/10.3390/ijms21072391
dc.identifier.issn16616596
dc.identifier.issn14220067
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/226725
dc.description.abstractPeroxisome 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, PPARa 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).
dc.language.isoen
dc.publisherMDPI
dc.sourceElements
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectPhysical Sciences
dc.subjectBiochemistry & Molecular Biology
dc.subjectChemistry, Multidisciplinary
dc.subjectChemistry
dc.subjectPPARs
dc.subjectlysosomes
dc.subjectNCoR1
dc.subjectPGC1 alpha
dc.subjectlipophagy
dc.subjectperoxisomes
dc.subjectautophagy
dc.subjectNAFLD
dc.subjectACTIVATED RECEPTOR-ALPHA
dc.subjectNUCLEAR RECEPTORS
dc.subjectAUTOPHAGY
dc.subjectLIVER
dc.subjectMETABOLISM
dc.subjectSTEATOHEPATITIS
dc.subjectLIPOPHAGY
dc.subjectLIPOLYSIS
dc.subjectSTORAGE
dc.subjectMICE
dc.typeReview
dc.date.updated2022-06-07T06:25:33Z
dc.contributor.departmentDEAN'S OFFICE (DUKE-NUS MEDICAL SCHOOL)
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.3390/ijms21072391
dc.description.sourcetitleINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
dc.description.volume21
dc.description.issue7
dc.published.statePublished
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