Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
4350621 | Neuroscience Letters | 2006 | 6 Pages |
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 Ï form of glutathione-S-transferases (GST-Ï)-positive OLGs during remyelination. Cultured primary OLGs displayed a strong correlation between protease M/neurosin and myelin basic protein (MBP). After tumor necrosis factor-α (TNF-α) and IFN-γ 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.
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Authors
Yoshio Bando, Shinji Ito, Yoshiko Nagai, Ryuji Terayama, Mari Kishibe, Ying-Ping Jiang, Branka Mitrovic, Takayuki Takahashi, Shigetaka Yoshida,