Journal article
IL-17A activates ERK1/2 and enhances differentiation of oligodendrocyte progenitor cells
Glia, Vol.63(5), pp.768-779
05/2015
DOI: 10.1002/glia.22783
PMCID: PMC4400118
PMID: 25557204
Abstract
Inflammatory signals present in demyelinated multiple sclerosis lesions affect the reparative remyelination process conducted by oligodendrocyte progenitor cells (OPCs). Interferon-γ (IFN-γ), tumor necrosis factor-α (TNF-α), and interleukin (IL)-6 have differing effects on the viability and growth of OPCs, however the effects of IL-17A are largely unknown. Primary murine OPCs were stimulated with IL-17A and their viability, proliferation, and maturation were assessed in culture. IL-17A-stimulated OPCs exited the cell cycle and differentiated with no loss in viability. Expression of the myelin-specific protein, proteolipid protein, increased in a cerebellar slice culture assay in the presence of IL-17A. Downstream, IL-17A activated ERK1/2 within 15 min and induced chemokine expression in 2 days. These results demonstrate that IL-17A exposure stimulates OPCs to mature and participate in the inflammatory response.
Details
- Title: Subtitle
- IL-17A activates ERK1/2 and enhances differentiation of oligodendrocyte progenitor cells
- Creators
- Jane M Rodgers - Northwestern UniversityAndrew P Robinson - Northwestern UniversityElen S Rosler - Free Form FibersKaren Lariosa-Willingham - Free Form FibersRachael E Persons - Medical College of WisconsinJason C Dugas - Free Form FibersStephen D Miller - Northwestern University
- Resource Type
- Journal article
- Publication Details
- Glia, Vol.63(5), pp.768-779
- DOI
- 10.1002/glia.22783
- PMID
- 25557204
- PMCID
- PMC4400118
- NLM abbreviation
- Glia
- ISSN
- 0894-1491
- eISSN
- 1098-1136
- Grant note
- R01 NS026543 / NINDS NIH HHS
- Language
- English
- Date published
- 05/2015
- Academic Unit
- Obstetrics and Gynecology
- Record Identifier
- 9984848509102771
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