4.7 Review

Cytosolic lipolysis and lipophagy: two sides of the same coin

Journal

NATURE REVIEWS MOLECULAR CELL BIOLOGY
Volume 18, Issue 11, Pages 671-684

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nrm.2017.76

Keywords

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Categories

Funding

  1. European Research Council ERC [340896]
  2. DKs Molecular Enzymology [W901]
  3. Metabolic and Cardiovascular Disease [W1226]
  4. SFB Lipotox [F30]
  5. Austrian Science Fund (FWF)
  6. Louis-Jeantet Foundation
  7. Fondation Leducq [12CVD04]
  8. BioTechMed-Graz flagship project EPIAge
  9. BioTechMed-Graz flagship project Lipid Signalling
  10. NAWI Graz
  11. BioTechMed-Graz (EPIAge)
  12. FWF [P29262, P29203, P27893]
  13. BMWFW
  14. University of Graz grant Unkonventionelle Forschung
  15. University of Graz grant Flysleep
  16. Austrian Science Fund (FWF) [P27070] Funding Source: Austrian Science Fund (FWF)
  17. European Research Council (ERC) [340896] Funding Source: European Research Council (ERC)

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Fatty acids are the most efficient substrates for energy production in vertebrates and are essential components of the lipids that form biological membranes. Synthesis of triacylglycerols from non-esterified free fatty acids (FFAs) combined with triacylglycerol storage represents a highly efficient strategy to stockpile FFAs in cells and prevent FFA-induced lipotoxicity. Although essentially all vertebrate cells have some capacity to store and utilize triacylglycerols, white adipose tissue is by far the largest triacylglycerol depot and is uniquely able to supply FFAs to other tissues. The release of FFAs from triacylglycerols requires their enzymatic hydrolysis by a process called lipolysis. Recent discoveries thoroughly altered and extended our understanding of lipolysis. This Review discusses how cytosolic 'neutral' lipolysis and lipophagy, which utilizes 'acid' lipolysis in lysosomes, degrade cellular triacylglycerols as well as how these pathways communicate, how they affect lipid metabolism and energy homeostasis and how their dysfunction affects the pathogenesis of metabolic diseases. Answers to these questions will likely uncover novel strategies for the treatment of prevalent metabolic diseases.

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