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Protective Effect of Cytosolic Phospholipase A2 Inhibition against Inflammation and Degeneration by Promoting Regulatory T Cells in Rats with Experimental Autoimmune Encephalomyelitis

Cytosolic phospholipase A2 (cPLA(2)) is the rate-limiting enzyme that initiates the production of various inflammatory mediators. Previous studies have shown that inhibiting cPLA(2) exerts a neuroprotective effect on experimental autoimmune encephalomyelitis (EAE) by ameliorating the severity of the...

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Detalles Bibliográficos
Autores principales: Yang, Dan, Ji, Hong-Fei, Zhang, Xue-Mei, Yue, Hui, Lin, Lin, Ma, Yu-Yan, Huang, Xiang-nan, Fu, Jin, Wang, Wei-Zhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3981565/
https://www.ncbi.nlm.nih.gov/pubmed/24782598
http://dx.doi.org/10.1155/2014/890139
Descripción
Sumario:Cytosolic phospholipase A2 (cPLA(2)) is the rate-limiting enzyme that initiates the production of various inflammatory mediators. Previous studies have shown that inhibiting cPLA(2) exerts a neuroprotective effect on experimental autoimmune encephalomyelitis (EAE) by ameliorating the severity of the disease and influencing Th1 and Th17 responses. However, it remains unclear whether treatment with a cPLA(2) inhibitor will influence the regulatory T cells (Tregs) that play a critical role in maintaining immune homeostasis and preventing autoimmune diseases. In this study, the cPLA(2) inhibitor AX059 reduced the onset and progression of EAE in Lewis rats. In addition, this effect was accompanied by activation of Tregs and alterations in the expression of their various cytokines. The study therefore demonstrated that Tregs are involved in the immunomodulatory effect mediated by cPLA(2) inhibition. These findings may have clinical application in the treatment of multiple sclerosis.