Requirement of Voltage-Gated Calcium Channel ß 4 Subunit for T Lymphocyte Functions

Author:

Badou Abdallah1234,Basavappa Srisaila1234,Desai Rooma1234,Peng You-Qing1234,Matza Didi1234,Mehal Wajahat Z.1234,Kaczmarek Leonard K.1234,Boulpaep Emile L.1234,Flavell Richard A.1234

Affiliation:

1. Section of Immunobiology, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06510, USA.

2. Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, CT 06510, USA.

3. Department of Pharmacology, Yale University School of Medicine, New Haven, CT 06510, USA.

4. Digestive Diseases Unit, Department of Medicine, Pharmacology and Physiology, University of Rochester School of Medicine.

Abstract

Calcium is known to play vital roles in diverse physiological processes, and it is known that voltage-gated calcium channels (Ca v ) mediate calcium influx in excitable cells. However, no consensus exists on the molecular identity of the calcium channels present in nonexcitable cells such as T lymphocytes. Here, we demonstrate that T lymphocytes express both regulatory β 4 and poreforming Ca v 1 α 1 subunits of Ca v channels. Ca v β 4 -mutant T lymphocytes fail to acquire normal functions and display impairment in the calcium response, activation of the transcription factor NFAT, and cytokine production. Although Ca v 1 channels of lymphocytes retain their voltage dependency, T cell receptor stimulation dramatically increases channel opening, providing a new mechanism for calcium entry in lymphocytes.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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