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1.
Nat Commun ; 14(1): 7844, 2023 Dec 06.
Article in English | MEDLINE | ID: mdl-38057317

ABSTRACT

Migration of T cells is essential for their ability to mount immune responses. Chemokine-induced T cell migration requires WNK1, a kinase that regulates ion influx into the cell. However, it is not known why ion entry is necessary for T cell movement. Here we show that signaling from the chemokine receptor CCR7 leads to activation of WNK1 and its downstream pathway at the leading edge of migrating CD4+ T cells, resulting in ion influx and water entry by osmosis. We propose that WNK1-induced water entry is required to swell the membrane at the leading edge, generating space into which actin filaments can polymerize, thereby facilitating forward movement of the cell. Given the broad expression of WNK1 pathway proteins, our study suggests that ion and water influx are likely to be essential for migration in many cell types, including leukocytes and metastatic tumor cells.


Subject(s)
Actin Cytoskeleton , Actins , Actins/metabolism , Polymerization , Cell Movement/physiology , Actin Cytoskeleton/metabolism , Signal Transduction/physiology
2.
J Exp Med ; 220(3)2023 03 06.
Article in English | MEDLINE | ID: mdl-36662229

ABSTRACT

Migration and adhesion play critical roles in B cells, regulating recirculation between lymphoid organs, migration within lymphoid tissue, and interaction with CD4+ T cells. However, there is limited knowledge of how B cells integrate chemokine receptor and integrin signaling with B cell activation to generate efficient humoral responses. Here, we show that the WNK1 kinase, a regulator of migration and adhesion, is essential in B cells for T-dependent and -independent antibody responses. We demonstrate that WNK1 transduces signals from the BCR, CXCR5, and CD40, and using intravital imaging, we show that WNK1 regulates migration of naive and activated B cells, and their interactions with T cells. Unexpectedly, we show that WNK1 is required for BCR- and CD40-induced proliferation, acting through the OXSR1 and STK39 kinases, and for efficient B cell-T cell collaboration in vivo. Thus, WNK1 is critical for humoral immune responses, by regulating B cell migration, adhesion, and T cell-dependent activation.


Subject(s)
Antibody Formation , B-Lymphocytes , Mice , Animals , Lymphoid Tissue , Signal Transduction , CD4-Positive T-Lymphocytes , CD40 Antigens/metabolism , WNK Lysine-Deficient Protein Kinase 1/metabolism
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