Central nervous system myelin: structure, function, and pathology

Charles M. Deber, Steven J. Reynolds

Research output: Contribution to journalReview article

Abstract

Multiple sclerosis (MS) and a number of related distinctive diseases are characterized by the active degradation of central nervous system (CNS) myelin, an axonal sheath comprised essentially of proteins and lipids. These demyelinating diseases appear to arise from complex interactions of genetic, immunological, infective, and biochemical mechanisms. While circumstances of MS etiology remain hypothetical, one persistent theme involves recognition by the immune system of myelin-specific antigens derived from myelin basic protein (MBP), the most abundant extrinsic myelin membrane protein, and/or another equally susceptible myelin protein or lipid component. Knowledge of the biochemical and physical-chemical properties of myelin proteins and lipids, particularly their composition, organization, structure, and accessibility with respect to the compacted myelin multilayers, thus becomes central to the understanding of how and why these antigens become selected during the development of MS. This review focuses on current understanding of the molecular basis underlying demyelinating disease as it may relate to the impact of the various protein and lipid components on myelin morphology; the precise molecular architecture of this membrane as dictated by protein-lipid and lipid-lipid interactions; and the relationship, if any, between the protein/lipid components and the destruction of myelin in pathological situations.

Original languageEnglish (US)
Pages (from-to)113-134
Number of pages22
JournalClinical Biochemistry
Volume24
Issue number2
DOIs
StatePublished - Apr 1991
Externally publishedYes

Keywords

  • central nervous system
  • encephalitogenic basic proteins
  • membrane proteins
  • multiple sclerosis
  • myelin proteins
  • nuclear magnetic resonance
  • protein conformation

ASJC Scopus subject areas

  • Clinical Biochemistry

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