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T cell migration requires ion and water influx to regulate actin polymerization

Author

Listed:
  • Leonard L. Boer

    (The Francis Crick Institute
    Department of Immunology and Inflammation, Imperial College London
    Karolinska Institutet)

  • Lesley Vanes

    (The Francis Crick Institute)

  • Serena Melgrati

    (The Francis Crick Institute
    Department of Immunology and Inflammation, Imperial College London
    Università della Svizzera Italiana)

  • Joshua Biggs O’May

    (The Francis Crick Institute)

  • Darryl Hayward

    (The Francis Crick Institute
    GSK)

  • Paul C. Driscoll

    (The Francis Crick Institute)

  • Jason Day

    (University of Cambridge)

  • Alexander Griffiths

    (London Metallomics Facility, Research Management & Innovation Directorate, King’s College London)

  • Renata Magueta

    (London Metallomics Facility, Research Management & Innovation Directorate, King’s College London)

  • Alexander Morrell

    (London Metallomics Facility, Research Management & Innovation Directorate, King’s College London)

  • James I. MacRae

    (The Francis Crick Institute)

  • Robert Köchl

    (The Francis Crick Institute
    Kings College London)

  • Victor L. J. Tybulewicz

    (The Francis Crick Institute)

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.

Suggested Citation

  • Leonard L. Boer & Lesley Vanes & Serena Melgrati & Joshua Biggs O’May & Darryl Hayward & Paul C. Driscoll & Jason Day & Alexander Griffiths & Renata Magueta & Alexander Morrell & James I. MacRae & Rob, 2023. "T cell migration requires ion and water influx to regulate actin polymerization," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43423-8
    DOI: 10.1038/s41467-023-43423-8
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    References listed on IDEAS

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    1. Yoav Benjamini & Abba M. Krieger & Daniel Yekutieli, 2006. "Adaptive linear step-up procedures that control the false discovery rate," Biometrika, Biometrika Trust, vol. 93(3), pages 491-507, September.
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    3. Alessandra Stangherlin & Joseph L. Watson & David C. S. Wong & Silvia Barbiero & Aiwei Zeng & Estere Seinkmane & Sew Peak Chew & Andrew D. Beale & Edward A. Hayter & Alina Guna & Alison J. Inglis & Ma, 2021. "Publisher Correction: Compensatory ion transport buffers daily protein rhythms to regulate osmotic balance and cellular physiology," Nature Communications, Nature, vol. 12(1), pages 1-1, December.
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