Critical role of WNK1 in MYC-dependent early mouse thymocyte development.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 33051000.
- Also identified by DOI 10.7554/eLife.56934 and PMC identifier 7591260.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
WNK1, a kinase that controls kidney salt homeostasis, also regulates adhesion and migration in CD4<sup>+</sup> T cells. <i>Wnk1</i> 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 β-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.
Medical subject headings
- Cell Differentiation
- Proto-Oncogene Proteins c-myc
- Thymocytes
- Thymus Gland
- WNK Lysine-Deficient Protein Kinase 1