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https://doi.org/10.3390/ijms21072391
Title: | Hepatic Lipid Catabolism via PPAR alpha-Lysosomal Crosstalk | Authors: | Sinha, Rohit A Rajak, Sangam Singh, Brijesh K Yen, Paul M |
Keywords: | Science & Technology Life Sciences & Biomedicine Physical Sciences Biochemistry & Molecular Biology Chemistry, Multidisciplinary Chemistry PPARs lysosomes NCoR1 PGC1 alpha lipophagy peroxisomes autophagy NAFLD ACTIVATED RECEPTOR-ALPHA NUCLEAR RECEPTORS AUTOPHAGY LIVER METABOLISM STEATOHEPATITIS LIPOPHAGY LIPOLYSIS STORAGE MICE |
Issue Date: | 1-Apr-2020 | Publisher: | MDPI | Citation: | Sinha, 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 | Abstract: | 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, 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). | Source Title: | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | URI: | https://scholarbank.nus.edu.sg/handle/10635/226725 | ISSN: | 16616596 14220067 |
DOI: | 10.3390/ijms21072391 |
Appears in Collections: | Staff Publications Elements |
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