Chemokine-dependent T cell migration requires aquaporin-3-mediated hydrogen peroxide uptake

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Abstract

Chemokine-dependent trafficking is indispensable for the effector function of antigenexperienced T cells during immune responses. In this study, we report that the water/glycerol channel aquaporin-3 (AQP3) is expressed on T cells and regulates their trafficking in cutaneous immune reactions. T cell migration toward chemokines is dependent on AQP3-mediated hydrogen peroxide (H2O2) uptake but not the canonical water/glycerol transport. AQP3-mediated H2O2 transport is essential for the activation of the Rho family GTPase Cdc42 and the subsequent actin dynamics. Coincidentally, AQP3-deficient mice are defective in the development of hapten-induced contact hypersensitivity, which is attributed to the impaired trafficking of antigen-primed T cells to the hapten-challenged skin. We therefore suggest that AQP3-mediated H2O2 uptake is required for chemokine-dependent T cell migration in sufficient immune response. © 2012 Hara-Chikuma et al.

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APA

Hara-Chikuma, M., Chikuma, S., Sugiyama, Y., Kabashima, K., Verkman, A. S., Inoue, S., & Miyachi, Y. (2012). Chemokine-dependent T cell migration requires aquaporin-3-mediated hydrogen peroxide uptake. Journal of Experimental Medicine, 209(10), 1743–1752. https://doi.org/10.1084/jem.20112398

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