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Calcium signalling in T cells

Journal

NATURE REVIEWS IMMUNOLOGY
Volume 19, Issue 3, Pages 154-169

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41577-018-0110-7

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Funding

  1. US National Institutes of Health [R01HL123364, R01HL097111, R21AG050072]
  2. Qatar National Research Fund (QNRF) [NPRP8-110-3-021]

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Calcium (Ca2+) signalling is of paramount importance to immunity. Regulated increases in cytosolic and organellar Ca2+ concentrations in lymphocytes control complex and crucial effector functions such as metabolism, proliferation, differentiation, antibody and cytokine secretion and cytotoxicity. Altered Ca2+ regulation in lymphocytes leads to various autoimmune, inflammatory and immunodeficiency syndromes. Several types of plasma membrane and organellar Ca2+-permeable channels are functional in T cells. They contribute highly localized spatial and temporal Ca2+ microdomains that are required for achieving functional specificity. While the mechanistic details of these Ca2+ microdomains are only beginning to emerge, it is evident that through crosstalk, synergy and feedback mechanisms, they fine-tune T cell signalling to match complex immune responses. In this article, we review the expression and function of various Ca2+-permeable channels in the plasma membrane, endoplasmic reticulum, mitochondria and endolysosomes of T cells and their role in shaping immunity and the pathogenesis of immune-mediated diseases.

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