CD8+ T Cells Require ITK-Mediated TCR Signaling for Migration to the Intestine

CD8+ T 细胞需要 ITK 介导的 TCR 信号传导才能迁移到肠道

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作者:Hyoung-Soo Cho, Soyoung Ha, Hyun Mu Shin, Andrea Reboldi, Jason A Hall, Jun R Huh, Edward J Usherwood, Leslie J Berg

Abstract

The Tec kinase IL-2-inducible T cell kinase (ITK) regulates the expression of TCR-induced genes. Itk-/- T cell responses are impaired but not absent. ITK inhibition prevented colitis disease progression and impaired T cell migration to the colon in mice. To examine the function of ITK in T cell migration to the intestine, we examined the number of gut T cells in Itk-/- mice and then evaluated their expression of gut-homing receptors. Combined with in vitro murine T cell stimulation and in vivo migration assay using congenic B6 mice, we demonstrated an essential role for ITK in T cell migration to the intestine in mice. Reconstitution of Itk-/- mouse CD8+ T cells with IFN regulatory factor 4 restored gut-homing properties, providing mechanistic insight into the function of ITK-mediated signaling in CD8+ T cell migration to the intestinal mucosa in mice.

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