Phosphatidylinositol-3 Phosphatase Myotubularin-Related Protein 6 Negatively Regulates CD4 T Cells

Author:

Srivastava Shekhar12,Ko Kyung12,Choudhury Papiya12,Li Zhai12,Johnson Amanda K.3,Nadkarni Vivek14,Unutmaz Derya3,Coetzee William A.15,Skolnik Edward Y.142

Affiliation:

1. Departments of Pharmacology

2. The Skirball Institute, New York University School of Medicine, New York, New York

3. Vanderbilt University Medical School, Department of Microbiology and Immunology, Nashville, Tennessee

4. Division of Nephrology

5. Pediatric Cardiology

Abstract

ABSTRACT Intracellular Ca 2+ levels rapidly rise following cross-linking of the T-cell receptor (TCR) and function as a critical intracellular second messenger in T-cell activation. It has been relatively under appreciated that K + channels play an important role in Ca 2+ influx into T lymphocytes by helping to maintain a negative membrane potential which provides an electrochemical gradient to drive Ca 2+ influx. Here we show that the Ca 2+ -activated K + channel, KCa3.1, which is critical for Ca 2+ influx in reactivated naive T cells and central memory T cells, requires phosphatidylinositol-3 phosphatase [PI(3)P] for activation and is inhibited by the PI(3)P phosphatase myotubularin-related protein 6 (MTMR6). Moreover, by inhibiting KCa3.1, MTMR6 functions as a negative regulator of Ca 2+ influx and proliferation of reactivated human CD4 T cells. These findings point to a new and unexpected role for PI(3)P and the PI(3)P phosphatase MTMR6 in the regulation of Ca 2+ influx in activated CD4 T cells and suggest that MTMR6 plays a critical role in setting a minimum threshold for a stimulus to activate a T cell.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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