Water channel aquaporin 4 is required for T cell receptor mediated lymphocyte activation

被引:2
|
作者
Nicosia, Michael [1 ]
Lee, Juyeun [2 ]
Beavers, Ashley [1 ]
Kish, Danielle [1 ]
Farr, George W. [3 ]
McGuirk, Paul R. [3 ]
Pelletier, Marc F. [3 ]
Lathia, Justin D.
Fairchild, Robert L.
Valujskikh, Anna [4 ]
机构
[1] Cleveland Clin, Lerner Res Inst, Dept Inflammat & Immun, 9500 Euclid Ave, Cleveland, OH 44195 USA
[2] Cleveland Clin, Lerner Res Inst, Dept Cardiovasc & Metab Sci, 9500 Euclid Ave, Cleveland, OH 44195 USA
[3] Aeromics Inc, 470 James St Suite 007, New Haven, CT 06513 USA
[4] Cleveland Clin, Lerner Res Inst, NB30,9500 Euclid Ave, Cleveland, OH 44195 USA
关键词
T lymphocytes; T cell receptors; receptor complex; signaling cascade; signal transduction; cell activation; aquaporin; 4; IMMUNOLOGICAL SYNAPSE; ACTIN CYTOSKELETON; MIGRATION; LOCALIZATION; INHIBITION; EXPRESSION; TRANSPORT;
D O I
10.1093/jleuko/qiad010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Our findings uncover a novel function of aquaporin 4 in T lymphocytes that facilitates TCR signaling and T cell activation via the actin cytoskeleton. Aquaporins are a family of ubiquitously expressed transmembrane water channels implicated in a broad range of physiological functions. We have previously reported that aquaporin 4 (AQP4) is expressed on T cells and that treatment with a small molecule AQP4 inhibitor significantly delays T cell mediated heart allograft rejection. Using either genetic deletion or small molecule inhibitor, we show that AQP4 supports T cell receptor mediated activation of both mouse and human T cells. Intact AQP4 is required for optimal T cell receptor (TCR)-related signaling events, including nuclear translocation of transcription factors and phosphorylation of proximal TCR signaling molecules. AQP4 deficiency or inhibition impairs actin cytoskeleton rearrangements following TCR crosslinking, causing inferior TCR polarization and a loss of TCR signaling. Our findings reveal a novel function of AQP4 in T lymphocytes and identify AQP4 as a potential therapeutic target for preventing TCR-mediated T cell activation.
引用
收藏
页码:544 / 554
页数:11
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