| Literature DB >> 21835646 |
Kyla Omilusik1, John J Priatel, Xiaoxi Chen, Yiwen Teresa Wang, Hongjian Xu, Kyung Bok Choi, Rayshad Gopaul, Adam McIntyre-Smith, Hung-Sia Teh, Rusung Tan, N Torben Bech-Hansen, Douglas Waterfield, David Fedida, Simon V Hunt, Wilfred A Jefferies.
Abstract
The transport of calcium ions (Ca(2+)) to the cytosol is essential for immunoreceptor signaling, regulating lymphocyte differentiation, activation, and effector function. Increases in cytosolic-free Ca(2+) concentrations are thought to be mediated through two interconnected and complementary mechanisms: the release of endoplasmic reticulum Ca(2+) "stores" and "store-operated" Ca(2+) entry via plasma membrane channels. However, the identity of molecular components conducting Ca(2+) currents within developing and mature T cells is unclear. Here, we have demonstrated that the L-type "voltage-dependent" Ca(2+) channel Ca(V)1.4 plays a cell-intrinsic role in the function, development, and survival of naive T cells. Plasma membrane Ca(V)1.4 was found to be essential for modulation of intracellular Ca(2+) stores and T cell receptor (TCR)-induced rises in cytosolic-free Ca(2+), impacting activation of Ras-extracellular signal-regulated kinase (ERK) and nuclear factor of activated T cells (NFAT) pathways. Collectively, these studies revealed that Ca(V)1.4 functions in controlling naive T cell homeostasis and antigen-driven T cell immune responses.Entities:
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Year: 2011 PMID: 21835646 DOI: 10.1016/j.immuni.2011.07.011
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745