| Literature DB >> 29374543 |
Madalina Duta-Mare1, Vinay Sachdev1, Christina Leopold1, Dagmar Kolb2, Nemanja Vujic1, Melanie Korbelius1, Dina C Hofer3, Wenmin Xia3, Katharina Huber3, Martina Auer1, Benjamin Gottschalk1, Christoph Magnes4, Wolfgang F Graier5, Andreas Prokesch1, Branislav Radovic5, Juliane G Bogner-Strauss6, Dagmar Kratky7.
Abstract
Lysosomal acid lipase (LAL) is the only known enzyme, which hydrolyzes cholesteryl esters and triacylglycerols in lysosomes of multiple cells and tissues. Here, we explored the role of LAL in brown adipose tissue (BAT). LAL-deficient (Lal-/-) mice exhibit markedly reduced UCP1 expression in BAT, modified BAT morphology with accumulation of lysosomes, and mitochondrial dysfunction, consequently leading to regular hypothermic events in mice kept at room temperature. Cold exposure resulted in reduced lipid uptake into BAT, thereby aggravating dyslipidemia and causing life threatening hypothermia in Lal-/- mice. Linking LAL as a potential regulator of lipoprotein lipase activity, we found Angptl4 mRNA expression upregulated in BAT. Our data demonstrate that LAL is critical for shuttling fatty acids derived from circulating lipoproteins to BAT during cold exposure. We conclude that inhibited lysosomal lipid hydrolysis in BAT leads to impaired thermogenesis in Lal-/- mice.Entities:
Keywords: Brown adipose tissue; Dyslipidemia; LAL deficiency; Lysosome; Thermogenesis; UCP1
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Year: 2018 PMID: 29374543 PMCID: PMC5839464 DOI: 10.1016/j.bbalip.2018.01.011
Source DB: PubMed Journal: Biochim Biophys Acta Mol Cell Biol Lipids ISSN: 1388-1981 Impact factor: 4.698