Decoding cell signalling and regulation of oligodendrocyte differentiation

Semin Cell Dev Biol. 2019 Nov:95:54-73. doi: 10.1016/j.semcdb.2018.05.020. Epub 2018 May 23.

Abstract

Oligodendrocytes are fundamental for the functioning of the nervous system; they participate in several cellular processes, including axonal myelination and metabolic maintenance for astrocytes and neurons. In the mammalian nervous system, they are produced through waves of proliferation and differentiation, which occur during embryogenesis. However, oligodendrocytes and their precursors continue to be generated during adulthood from specific niches of stem cells that were not recruited during development. Deficiencies in the formation and maturation of these cells can generate pathologies mainly related to myelination. Understanding the mechanisms involved in oligodendrocyte development, from the precursor to mature cell level, will allow inferring therapies and treatments for associated pathologies and disorders. Such mechanisms include cell signalling pathways that involve many growth factors, small metabolic molecules, non-coding RNAs, and transcription factors, as well as specific elements of the extracellular matrix, which act in a coordinated temporal and spatial manner according to a given stimulus. Deciphering those aspects will allow researchers to replicate them in vitro in a controlled environment and thus mimic oligodendrocyte maturation to understand the role of oligodendrocytes in myelination in pathologies and normal conditions. In this study, we review these aspects, based on the most recent in vivo and in vitro data on oligodendrocyte generation and differentiation.

Keywords: Cell reprogramming; Extracellular matrix; Myelination; Non-coding RNAs; Oligodendrogenesis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cell Differentiation*
  • Extracellular Matrix / metabolism
  • Humans
  • Myelin Sheath / metabolism
  • Neural Stem Cells / cytology
  • Neural Stem Cells / metabolism
  • Oligodendroglia / cytology*
  • Oligodendroglia / metabolism*
  • Signal Transduction*