p38 alpha MAP Kinase Controls IL-17 Synthesis in Vogt-Koyanagi-Harada Syndrome and Experimental Autoimmune Uveitis
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2010
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Resumo |
PURPOSE. Interleukin (IL)-17, which is responsible for the initial influx of leukocytes into the target tissue, was recently described as the main cytokine involved in autoimmune diseases. Vogt-Koyanagi-Harada (VKH) syndrome is a significant cause of noninfectious blindness in the world. Herein the authors aimed at unraveling the involvement of IL-17 in VKH and in experimental autoimmune uveitis, focusing on the signaling pathways involved in IL-17 synthesis. METHODS. Mice were immunized with 161-180 peptide and pertussis toxin. Draining lymph node cells, harvested 21 days after immunization, were cultured in the presence or absence of p38 alpha mitogen-activated protein kinase (MAPK) inhibitor (SB203580) and assayed for cytokine production and quantification of CD4(+)IL-17(+) cells. Mice received intraocular injections of SB203580, and disease severity was evaluated by histologic examination of the enucleated eyes at day 21. CD4(+) lymphocytes from MSK-1/2-deficient mice, human CD4(+) cells silenced with MSK1 siRNA, or peripheral blood mononuclear cells (PBMCs) from VKH patients were cultured in the presence or absence of p38 alpha MAPK inhibitor and then assayed for IL-17, IFN-gamma, and IL-4 production. RESULTS. The inhibition of p38 alpha MAPK fully blocked the synthesis of IL-17 by PBMCs from VKH patients and lymphocytes from EAU mice. The absence of the msk1/2 gene resulted in failure to produce IL-17 by murine and human lymphocytes. Interestingly, intraocular injections of SB203580 in EAU mice did not suppress development of the disease. CONCLUSIONS. These data show that p38 alpha MAPK-MSK1/2 is involved in the control of IL-17 synthesis by CD4(+) T cells and that inhibition of p38 alpha MAPK in vitro suppresses IL-17 synthesis but that inhibition of this kinase in vivo did not protect from EAU. (Invest Ophthalmol Vis Sci. 2010;51:3567-3574) DOI: 10.1167/iovs.09-4393 Sao Paulo State Science Council[01/02584-2] Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) CAPESP (Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior)[PNPD 0188085] |
Identificador |
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, v.51, n.7, p.3567-3574, 2010 0146-0404 http://producao.usp.br/handle/BDPI/28269 10.1167/iovs.09-4393 |
Idioma(s) |
eng |
Publicador |
ASSOC RESEARCH VISION OPHTHALMOLOGY INC |
Relação |
Investigative Ophthalmology & Visual Science |
Direitos |
restrictedAccess Copyright ASSOC RESEARCH VISION OPHTHALMOLOGY INC |
Palavras-Chave | #ACTIVATED PROTEIN-KINASE #CD4(+) T-CELLS #MULTIPLE-SCLEROSIS #EFFECTOR RESPONSE #TH17 CELLS #IFN-GAMMA #DISEASE #UVEORETINITIS #MICE #DIFFERENTIATION #Ophthalmology |
Tipo |
article original article publishedVersion |