Stimulation of in vitro myelin synthesis by microglia

Glia. 1994 Aug;11(4):326-35. doi: 10.1002/glia.440110405.

Abstract

Central nervous system myelin is elaborated by oligodendrocytes, which have been studied extensively in cell culture. Dissociated brain cultures allow in vitro analysis of events in myelinogenesis, including cell-cell interactions. Microglia, the primary phagocytic cell of the central nervous system, appear in developing fiber tracts prior to the onset of myelination in vivo. To gain insight into potential oligodendrocyte-microglial interactions during development, these cells were co-cultured and various parameters of myelin synthesis were measured. In co-culture, microglia stimulated the synthesis of sulfatide, a myelin-specific galactolipid, in oligodendrocytes, as well as the expression of the myelin-specific proteins myelin basic protein and proteolipid protein. Activity of the oligodendrocyte cytoplasm-specific enzyme 2',3'-cyclic nucleotide 3'-phosphohydrolase was not elevated, suggesting that the effects of microglia were not due to stimulation of oligodendrocyte proliferation. This was confirmed by the inability of microglia to induce significant DNA synthesis. Conditioned medium from cultured microglia provided a similar stimulatory activity, suggesting that the increase in myelin synthesis does not require contact between oligodendrocytes and microglia. These findings suggest a stimulatory role for microglia during myelinogenesis.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 2',3'-Cyclic Nucleotide 3'-Phosphodiesterase
  • 2',3'-Cyclic-Nucleotide Phosphodiesterases / metabolism
  • Animals
  • Immunoblotting
  • Microglia / enzymology
  • Microglia / physiology*
  • Microscopy, Electron
  • Myelin Sheath / metabolism*
  • Nerve Fibers / metabolism
  • Nerve Tissue Proteins / biosynthesis
  • Oligodendroglia / enzymology
  • Oligodendroglia / physiology
  • Phosphoric Diester Hydrolases*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Nerve Tissue Proteins
  • 2',3'-Cyclic-Nucleotide Phosphodiesterases
  • Phosphoric Diester Hydrolases
  • 2',3'-Cyclic Nucleotide 3'-Phosphodiesterase
  • Cnp protein, rat