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2000
Volume 18, Issue 5
  • ISSN: 1566-5240
  • E-ISSN: 1875-5666

Abstract

Background: MicroRNA-19b (miR-19b) is essential in determining oligodendroglia proliferation. Phosphatase and tensin homologue on chromosome 10 (PTEN) is considered the target of miR-19b and participates in oligodendrocyte differentiation and proliferation. Methods: Murine EAE was induced by myelin oligodendrocyte glycoprotein (MOG35– 55). For EAE reversal, artificially synthesized agomiR-19b was intravenous injected after immunization. Results: We found that the expression of miR-19b is significantly reduced in an experimental autoimmune encephalomyelitis (EAE) mouse model. This downregulation, which is associated with the neurological scores, can be dramatically ameliorated by agomiR-19b. Our results show that agomiR-19b increases the expression of myelin basic protein (MBP) and cyclic nucleotide phosphodiesterase (CNP), which are regularly utilized as molecular markers of oligodendrocytes. Furthermore, our study also revealed that miR-19b probably affects the expression of PTEN in the EAE model. Conclusion: These results indicate that the restoration of miR-19b probably exerts its therapeutic effect by affecting PTEN in the pathogenesis of EAE.

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/content/journals/cmm/10.2174/1566524018666181004123716
2018-06-01
2025-09-01
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/content/journals/cmm/10.2174/1566524018666181004123716
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  • Article Type:
    Research Article
Keyword(s): agomiR-19b; CNP; experimental autoimmune encephalomyelitis; MBP; MiR-19b; oligodendrocyte; PTEN
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