The Yin and Yang of cell cycle progression and differentiation in the oligodendroglial lineage

Ment Retard Dev Disabil Res Rev. 2006;12(2):85-96. doi: 10.1002/mrdd.20103.

Abstract

In white matter disorders such as leukodystrophies (LD), periventricular leucomalacia (PVL), or multiple sclerosis (MS), the hypomyelination or the remyelination failure by oligodendrocyte progenitor cells involves errors in the sequence of events that normally occur during development when progenitors proliferate, migrate through the white matter, contact the axon, and differentiate into myelin-forming oligodendrocytes. Multiple mechanisms underlie the eventual progressive deterioration that typifies the natural history of developmental demyelination in LD and PVL and of adult-onset demyelination in MS. Over the past few years, pathophysiological studies have mostly focused on seeking abnormalities that impede oligodendroglial maturation at the level of migration, myelination, and survival. In contrast, there has been a strikingly lower interest for early proliferative and differentiation events that are likely to be equally critical for white matter development and myelin repair. This review highlights the Yin and Yang principles of interactions between intrinsic factors that coordinately regulate progenitor cell division and the onset of differentiation, i.e. the initial steps of oligodendrocyte lineage progression that are obviously crucial in health and diseases.

Publication types

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

MeSH terms

  • Adult
  • Cell Cycle / physiology*
  • Cell Differentiation / physiology*
  • Cell Lineage / physiology*
  • Cyclin E / physiology
  • Cyclin-Dependent Kinase 2 / genetics
  • Cyclin-Dependent Kinase Inhibitor p18 / physiology
  • Cyclin-Dependent Kinase Inhibitor p27 / physiology
  • Demyelinating Diseases / genetics
  • Demyelinating Diseases / pathology
  • Humans
  • Infant, Newborn
  • Leukomalacia, Periventricular / genetics
  • Leukomalacia, Periventricular / pathology
  • Multiple Sclerosis / pathology
  • Myelin Sheath / genetics
  • Myelin Sheath / pathology
  • Oligodendroglia / pathology*
  • Phosphorylation
  • Stem Cells / pathology

Substances

  • Cyclin E
  • Cyclin-Dependent Kinase Inhibitor p18
  • Cyclin-Dependent Kinase Inhibitor p27
  • Cyclin-Dependent Kinase 2