Critical role of WNK1 in MYC-dependent early mouse thymocyte development

被引:12
作者
Kochl, Robert [1 ,2 ]
Vanes, Lesley [1 ]
Sopena, Miriam Llorian [1 ]
Chakravarty, Probir [1 ]
Hartweger, Harald [1 ]
Fountain, Kathryn [1 ]
White, Andrea [3 ]
Cowan, Jennifer [3 ]
Anderson, Graham [3 ]
Tybulewicz, Victor L. J. [1 ,4 ]
机构
[1] Francis Crick Inst, London, England
[2] Kings Coll London, London, England
[3] Univ Birmingham, Birmingham, W Midlands, England
[4] Imperial Coll, London, England
基金
英国惠康基金; 英国医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
T-CELL DEVELOPMENT; BETA-SELECTION CHECKPOINT; C-MYC; PRE-T; INDUCED PROLIFERATION; PROTEIN-KINASES; MICE; EXPRESSION; RECEPTOR; ACTIVATION;
D O I
10.7554/eLife.56934
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
WNK1, a kinase that controls kidney salt homeostasis, also regulates adhesion and migration in CD4(+) T cells. Wnk1 is highly expressed in thymocytes, and since migration is important for thymocyte maturation, we investigated a role for WNK1 in mouse thymocyte development. We find that WNK1 is required for the transition of double negative (DN) thymocytes through the beta-selection checkpoint and subsequent proliferation and differentiation into double positive (DP) thymocytes. Furthermore, we show that WNK1 negatively regulates LFA1-mediated adhesion and positively regulates CXCL12-induced migration in DN thymocytes. Despite this, migration defects of WNK1-deficient thymocytes do not account for the developmental arrest. Instead, we show that in DN thymocytes WNK1 transduces pre-TCR signals via OXSR1 and STK39 kinases, and the SLC12A2 ion co-transporter that are required for post-transcriptional upregulation of MYC and subsequent proliferation and differentiation into DP thymocytes. Thus, a pathway regulating ion homeostasis is a critical regulator of thymocyte development.
引用
收藏
页码:1 / 32
页数:32
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