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Peroxisomes, lipid metabolism and lipotoxicity

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.bbalip.2010.01.001

Keywords

Fatty acid oxidation; Fatty acid; Plasmalogen; Bile acid; Zellweger syndrome; Adrenoleukodystrophy; Refsum disease

Funding

  1. European Leukodystrophy Association [ELA 2008-05111A]
  2. Netherlands Organization for Scientific Research (VIDI) [016.086.328]

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Peroxisomes play an essential role in cellular lipid metabolism as exemplified by the existence of a number of genetic diseases in humans caused by the impaired function of one of the peroxisomal enzymes involved in lipid metabolism. Key pathways in which peroxisomes are involved include: (1.) fatty acid beta-oxidation; (2.) etherphospholipid biosynthesis, and (3.) fatty acid alpha-oxidation. In this paper we will describe these different pathways in some detail and will provide an overview of peroxisomal disorders of metabolism and in addition discuss the toxicity of the intermediates of peroxisomal metabolism as they accumulate in the different peroxisomal deficiencies. (C) 2010 Elsevier B.V. All rights reserved.

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