ABHD15 regulates adipose tissue lipolysis and hepatic lipid accumulation

Mol Metab. 2019 Jul:25:83-94. doi: 10.1016/j.molmet.2019.05.002. Epub 2019 May 6.

Abstract

Objective: Insulin suppresses adipose tissue lipolysis after a meal, playing a key role in metabolic homeostasis. This is mediated via the kinase Akt and its substrate phosphodiesterase 3B (PDE3B). Once phosphorylated and activated, PDE3B hydrolyses cAMP leading to the inactivation of cAMP-dependent protein kinase (PKA) and suppression of lipolysis. However, several gaps have emerged in this model. Here we investigated the role of the PDE3B-interacting protein, α/β-hydrolase ABHD15 in this process.

Methods: Lipolysis, glucose uptake, and signaling were assessed in ABHD15 knock down and knock out adipocytes and fat explants in response to insulin and/or β-adrenergic receptor agonist. Glucose and fatty acid metabolism were determined in wild type and ABHD15-/- littermate mice.

Results: Deletion of ABHD15 in adipocytes resulted in a significant defect in insulin-mediated suppression of lipolysis with no effect on insulin-mediated glucose uptake. ABHD15 played a role in suppressing PKA signaling as phosphorylation of the PKA substrate Perilipin-1 remained elevated in response to insulin upon ABHD15 deletion. ABHD15-/- mice had normal glucose metabolism but defective fatty acid metabolism: plasma fatty acids were elevated upon fasting and in response to insulin, and this was accompanied by elevated liver triglycerides upon β-adrenergic receptor activation. This is likely due to hyperactive lipolysis as evident by the larger triglyceride depletion in brown adipose tissue in these mice. Finally, ABHD15 protein levels were reduced in adipocytes from mice fed a Western diet, further implicating this protein in metabolic homeostasis.

Conclusions: Collectively, ABHD15 regulates adipocyte lipolysis and liver lipid accumulation, providing novel therapeutic opportunities for modulating lipid homeostasis in disease.

Keywords: Adipocytes; Fatty acid metabolism; Insulin action; Lipolysis; β-adrenergic receptor agonist.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipocytes / metabolism
  • Adipose Tissue / drug effects
  • Adipose Tissue / metabolism*
  • Animals
  • Carbohydrate Metabolism
  • Carboxylic Ester Hydrolases / genetics
  • Carboxylic Ester Hydrolases / metabolism*
  • Carboxylic Ester Hydrolases / pharmacology
  • Cyclic AMP-Dependent Protein Kinases / metabolism*
  • Cyclic Nucleotide Phosphodiesterases, Type 3 / metabolism
  • Fasting
  • Fatty Acids / blood
  • Glucose / metabolism
  • Homeostasis
  • Insulin / metabolism
  • Lipid Accumulation Product / physiology*
  • Lipid Metabolism
  • Lipolysis / drug effects
  • Lipolysis / physiology*
  • Liver / metabolism*
  • Male
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Membrane Proteins / pharmacology
  • Mice
  • Mice, Knockout
  • Perilipin-1 / metabolism
  • Phosphorylation
  • Signal Transduction
  • Triglycerides

Substances

  • Fatty Acids
  • Insulin
  • Membrane Proteins
  • Perilipin-1
  • Triglycerides
  • Cyclic AMP-Dependent Protein Kinases
  • Abhd15 protein, mouse
  • Carboxylic Ester Hydrolases
  • Cyclic Nucleotide Phosphodiesterases, Type 3
  • Glucose