Etiology and treatment of adrenoleukodystrophy: new insights from Drosophila

Dis Model Mech. 2018 Jun 15;11(6):dmm031286. doi: 10.1242/dmm.031286.

Abstract

Adrenoleukodystrophy (ALD) is a fatal progressive neurodegenerative disorder affecting brain white matter. The most common form of ALD is X-linked (X-ALD) and results from mutation of the ABCD1-encoded very-long-chain fatty acid (VLCFA) transporter. X-ALD is clinically heterogeneous, with the cerebral form being the most severe. Diagnosed in boys usually between the ages of 4 and 8 years, cerebral X-ALD symptoms progress rapidly (in as little as 2 years) through declines in cognition, learning and behavior, to paralysis and ultimately to a vegetative state and death. Currently, there are no good treatments for X-ALD. Here, we exploit the Drosophila bubblegum (bgm) double bubble (dbb) model of neurometabolic disease to expand diagnostic power and therapeutic potential for ALD. We show that loss of the Drosophila long-/very-long-chain acyl-CoA synthetase genes bgm and/or dbb is indistinguishable from loss of the Drosophila ABC transporter gene ABCD Shared loss-of-function phenotypes for synthetase and transporter mutants point to a lipid metabolic pathway association with ALD-like neurodegenerative disease in Drosophila; a pathway association that has yet to be established in humans. We also show that manipulation of environment increases the severity of neurodegeneration in bgm and dbb mutant flies, adding even further to a suite of new candidate ALD disease-causing genes and pathways in humans. Finally, we show that it is a lack of lipid metabolic pathway product and not (as commonly thought) an accumulation of pathway precursor that is causative of neurometabolic disease: addition of medium-chain fatty acids to the diet of bgm or dbb mutant flies prevents the onset of neurodegeneration. Taken together, our data provide new foundations both for diagnosing ALD and for designing effective, mechanism-based treatment protocols.This article has an associated First Person interview with the first author of the paper.

Keywords: ABCD1; Bubblegum (Bgm); Double bubble (Dbb); Elongase; Fatty acid acyl-coA synthetase; Fatty acid transporter; Neurodegeneration.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenoleukodystrophy / complications
  • Adrenoleukodystrophy / etiology*
  • Adrenoleukodystrophy / genetics
  • Adrenoleukodystrophy / therapy*
  • Animals
  • Central Nervous System / pathology
  • Drosophila Proteins / metabolism
  • Drosophila melanogaster / physiology*
  • Fatty Acids / metabolism
  • Gene-Environment Interaction
  • Mutation / genetics
  • Nerve Degeneration / complications
  • Nerve Degeneration / pathology
  • Penetrance
  • Retinal Neurons / metabolism

Substances

  • Drosophila Proteins
  • Fatty Acids