Lipid metabolism in myelinating glial cells: lessons from human inherited disorders and mouse models

被引:226
作者
Chrast, Roman [1 ]
Saher, Gesine [2 ]
Nave, Klaus-Armin [2 ]
Verheijen, Mark H. G. [3 ]
机构
[1] Univ Lausanne, Dept Med Genet, CH-1015 Lausanne, Switzerland
[2] Max Planck Inst Expt Med, Dept Neurogenet, Gottingen, Germany
[3] Vrije Univ Amsterdam, Ctr Neurogenom & Cognit Res, Dept Mol & Cellular Neurobiol, Amsterdam, Netherlands
基金
瑞士国家科学基金会;
关键词
LEMLI-OPITZ-SYNDROME; SJOGREN-LARSSON-SYNDROME; PERIPHERAL NERVOUS-SYSTEM; FATTY-ACID COMPOSITION; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; PYRUVATE-CARBOXYLASE DEFICIENCY; GENOTYPE-PHENOTYPE CORRELATION; COA REDUCTASE INHIBITOR; LIVER PLASMA MEMBRANES; NIEMANN-PICK-DISEASE;
D O I
10.1194/jlr.R009761
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The integrity of central and peripheral nervous system myelin is affected in numerous lipid metabolism disorders. This vulnerability was so far mostly attributed to the extraordinarily high level of lipid synthesis that is required for the formation of myelin, and to the relative autonomy in lipid synthesis of myelinating glial cells because of blood barriers shielding the nervous system from circulating lipids. Recent insights from analysis of inherited lipid disorders, especially those with prevailing lipid depletion and from mouse models with glia-specific disruption of lipid metabolism, shed new light on this issue. The particular lipid composition of myelin, the transport of lipid-associated myelin proteins, and the necessity for timely assembly of the myelin sheath all contribute to the observed vulnerability of myelin to perturbed lipid metabolism. Furthermore, the uptake of external lipids may also play a role in the formation of myelin membranes. jlr In addition to an improved understanding of basic myelin biology, these data provide a foundation for future therapeutic interventions aiming at preserving glial cell integrity in metabolic disorders.-Chrast, R., G. Saher, K-A. Nave, and M. H. G. Verheijen. Lipid metabolism in myelinating glial cells: lessons from human inherited disorders and mouse models. J. Lipid Res. 2011. 52: 419-434.
引用
收藏
页码:419 / 434
页数:16
相关论文
共 180 条
  • [91] Lazarow P.B., 1989, METABOLIC BASIS INHE, VII, P1479
  • [92] Ledeen RW, 2006, ADV EXP MED BIOL, V576, P131
  • [93] Lipid-protein interactions in biological membranes: a structural perspective
    Lee, AG
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2003, 1612 (01): : 1 - 40
  • [94] Cerebrotendinous xanthomatosis - Possible higher prevalence than previously recognized
    Lorincz, MT
    Rainier, S
    Thomas, D
    Fink, JK
    [J]. ARCHIVES OF NEUROLOGY, 2005, 62 (09) : 1459 - 1463
  • [95] Defective N-acetylaspartate catabolism reduces brain acetate levels and myelin lipid synthesis in Canavan's disease
    Madhavarao, CN
    Arun, P
    Moffett, JR
    Szucs, S
    Surendran, S
    Matalon, R
    Garbern, J
    Hristova, D
    Johnson, A
    Jiang, W
    Namboodiri, MAA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (14) : 5221 - 5226
  • [96] Immunohistochemical localization of asparoacylase in the rat central nervous system
    Madhavarao, CN
    Moffett, JR
    Moore, RA
    Viola, RE
    Namboodiri, MAA
    Jacobowitz, DM
    [J]. JOURNAL OF COMPARATIVE NEUROLOGY, 2004, 472 (03) : 318 - 329
  • [97] Lovastatin Induces the Formation of Abnormal Myelin-Like Membrane Sheets in Primary Oligodendrocytes
    Maier, Olaf
    De Jonge, Jenny
    Nomden, Anita
    Hoekstra, Dick
    Baron, Wia
    [J]. GLIA, 2009, 57 (04) : 402 - 413
  • [98] Sulfatide is essential for the maintenance of CNS myelin and axon structure
    Marcus, J
    Honigbaum, S
    Shroff, S
    Honke, K
    Rosenbluth, J
    Dupree, JL
    [J]. GLIA, 2006, 53 (04) : 372 - 381
  • [99] Pyruvate carboxylase deficiency: Mechanisms, mimics and anaplerosis
    Marin-Valencia, Isaac
    Roe, Charles R.
    Pascual, Juan M.
    [J]. MOLECULAR GENETICS AND METABOLISM, 2010, 101 (01) : 9 - 17
  • [100] Spongy degeneration of the brain, Canavan disease: Biochemical and molecular findings
    Matalon, R
    Michals-Matalon, K
    [J]. FRONTIERS IN BIOSCIENCE-LANDMARK, 2000, 5 : D307 - D311