Journal
JOURNAL OF EXPERIMENTAL MEDICINE
Volume 202, Issue 6, Pages 841-851Publisher
ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20050665
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Experimental autoimmune encephalomyelitis (EAE), a Th1-mediated inflammatory disease of the central nervous system (CNS), is a model of human multiple sclerosis. Cytosolic phospholipase A(2)alpha ( cPLA(2)alpha), which initiates production of prostaglandins, leukotrienes, and platelet-activating factor, is present in EAE lesions. Using myelin oligodendrocyte glycoprotein (MOG) immunization, as well as an adoptive transfer model, we showed that cPLA2(alpha)(-/-) mice are resistant to EAE. Histologic examination of the CNS from MOG-immunized mice revealed extensive inflammatory lesions in the cPLA(2)alpha(+/+) mice, whereas the lesions in cPLA(2)alpha(-/-) mice were reduced greatly or completely absent. MOG-specific T cells generated from WT mice induced less severe EAE in cPLA(2)alpha(-/-) mice compared with cPLA2 alpha(-/-) mice, which indicates that cPLA(2)alpha plays a role in the effector phase of EAE. Additionally, MOG-specific T cells from cPLA(2)alpha(-/-) mice, transferred into WT mice, induced EAE with delayed onset and lower severity compared with EAE that was induced by control cells; this indicates that cPLA(2)alpha also plays a role in the induction phase of EAE. MOG-specific T cells from cPLA(2)alpha(-/-) mice were deficient in production of Th1-type cytokines. Consistent with this deficiency, in vivo administration of IL-12 rendered cPLA(2)alpha(-/-) mice susceptible to EAE. Our data indicate that cPLA(2)alpha plays an important role in EAE development and facilitates differentiation of T cells toward the Th1 phenotype.
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