Distinct roles for matrix metalloproteinase-2 and α4 integrin in autoimmune T cell extravasation and residency in brain parenchyma during experimental autoimmune encephalomyelitis

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Abstract

Expression of α4 integrin by auto-reactive T cells is critical for their ability to induce EAE, an autoimmune disease of the central nervous system in mice, used as a model to study human multiple sclerosis. Having previously identified one role for α4 integrin in adhesion-mediated induction of matrix metalloproteinase-2 (MMP-2), an enzyme that degrades the subendothelial basement membrane matrix, we investigated independent roles for MMP-2 and α4 integrin during EAE. The data suggest that expression of α4 integrin by auto-reactive T cells is important not only in mediating MMP- 2 induction to facilitate entry into the CNS, but also plays a role in maintaining residency within the CNS. (C) 2000 Elsevier Science B.V.

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Graesser, D., Mahooti, S., & Madri, J. A. (2000). Distinct roles for matrix metalloproteinase-2 and α4 integrin in autoimmune T cell extravasation and residency in brain parenchyma during experimental autoimmune encephalomyelitis. Journal of Neuroimmunology, 109(2), 121–131. https://doi.org/10.1016/S0165-5728(00)00275-7

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