Implications of protease M/neurosin in myelination during experimental demyelination and remyelination

Neurosci Lett. 2006 Sep 25;405(3):175-80. doi: 10.1016/j.neulet.2006.06.030. Epub 2006 Aug 4.

Abstract

Protease M/neurosin is a serine protease expressed by oligodendrocytes (OLGs) in the central nervous system (CNS). To investigate the role of protease M/neurosin during experimental demyelination and remyelination, mice were fed cuprizone (bis-cyclohexanon oxaldihydrazone). Semi-quantitative RT-PCR analysis and immunohistochemistry revealed that the expressions of protease M/neurosin mRNA and protein were rapidly reduced in demyelination, whereas the expression of protease M/neurosin was increased in pi form of glutathione-S-transferases (GST-pi)-positive OLGs during remyelination. Cultured primary OLGs displayed a strong correlation between protease M/neurosin and myelin basic protein (MBP). After tumor necrosis factor-alpha (TNF-alpha) and IFN-gamma stimulation, these proteins showed colocalization in the oligodendroglial process. The suppression of protease M/neurosin using RNAi reduced the level of MBP mRNA in cultured OLGs. In contrast, the reduced level of protease M/neurosin was not associated with oligodendroglial cell death or differentiation in cultured OLGs. This study identifies that protease M/neurosin in OLGs is closely associated with the expression of the MBP and the PLP gene. Our data emphasize that the maintenance of myelination is an important function of protease M/neurosin in OLGs, suggesting its relation to the oligodendroglial response to myelin disorders.

Publication types

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

MeSH terms

  • 2',3'-Cyclic-Nucleotide Phosphodiesterases / metabolism
  • Animals
  • Cells, Cultured
  • Cuprizone / toxicity
  • Demyelinating Diseases / chemically induced
  • Demyelinating Diseases / metabolism*
  • Demyelinating Diseases / pathology
  • Demyelinating Diseases / physiopathology*
  • Disease Models, Animal
  • Glutathione S-Transferase pi / metabolism
  • Immunohistochemistry / methods
  • Interferon-gamma / pharmacology
  • Kallikreins / genetics
  • Kallikreins / physiology*
  • Mice
  • Mice, Inbred BALB C
  • Monoamine Oxidase Inhibitors / toxicity
  • Myelin Basic Protein / genetics
  • Myelin Basic Protein / metabolism
  • Myelin Sheath / metabolism*
  • Oligodendroglia / drug effects
  • Oligodendroglia / metabolism
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / pharmacology
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Time Factors
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Monoamine Oxidase Inhibitors
  • Myelin Basic Protein
  • RNA, Messenger
  • RNA, Small Interfering
  • Tumor Necrosis Factor-alpha
  • Cuprizone
  • Interferon-gamma
  • Glutathione S-Transferase pi
  • 2',3'-Cyclic-Nucleotide Phosphodiesterases
  • Kallikreins
  • Prss18 protein, mouse