Phosphatidylinositol-3 phosphatase myotubularin-related protein 6 negatively regulates CD4 T cells

被引:41
作者
Srivastava, Shekhar
Ko, Kyung
Choudhury, Papiya
Li, Zhai
Johnson, Amanda K.
Nadkarni, Vivek
Unutmaz, Derya
Coetzee, William A.
Skolnik, Edward Y.
机构
[1] NYU, Sch Med, Skirball Inst, New York, NY 10016 USA
[2] NYU, Sch Med, Dept Pharmacol, New York, NY 10016 USA
[3] NYU, Sch Med, Dept Pediat Cardiol, New York, NY 10016 USA
[4] NYU, Sch Med, Div Nephrol, New York, NY 10016 USA
[5] Vanderbilt Univ, Sch Med, Dept Microbiol & Immunol, Nashville, TN USA
关键词
D O I
10.1128/MCB.00352-06
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Intracellular Ca2+ 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 Ca2+ influx into T lymphocytes by helping to maintain a negative membrane potential which provides an electrochemical gradient to drive Ca2+ influx. Here we show that the Ca2+-activated K+ channel, KCa3.1, which is critical for Ca2+ 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 Ca2+ 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 Ca2+ 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.
引用
收藏
页码:5595 / 5602
页数:8
相关论文
共 30 条
[1]   ELEVATION OF INTRACELLULAR CALCIUM REDUCES VOLTAGE-DEPENDENT POTASSIUM CONDUCTANCE IN HUMAN T-CELLS [J].
BREGESTOVSKI, P ;
REDKOZUBOV, A ;
ALEXEEV, A .
NATURE, 1986, 319 (6056) :776-778
[2]   Molecular properties and physiological roles of ion channels in the immune system [J].
Cahalan, MD ;
Wulff, H ;
Chandy, KG .
JOURNAL OF CLINICAL IMMUNOLOGY, 2001, 21 (04) :235-252
[3]   NFAT signaling: Choreographing the social lives of cells [J].
Crabtree, GR ;
Olson, EN .
CELL, 2002, 109 :S67-S79
[4]  
Dang H, 2004, MOL BIOL CELL, V15, P189, DOI 10.1091/mbc.E03-08-0605
[5]   Calcium-activated potassium channels sustain calcium signaling in T lymphocytes - Selective blockers and manipulated channel expression levels [J].
Fanger, CM ;
Rauer, H ;
Neben, AL ;
Miller, MJ ;
Rauer, H ;
Wulff, H ;
Rosa, JC ;
Ganellin, CR ;
Chandy, KG ;
Cahalan, MD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (15) :12249-12256
[6]   Gene regulation mediated by calcium signals in T lymphocytes [J].
Feske, S ;
Giltnane, J ;
Dolmetsch, R ;
Staudt, LM ;
Rao, A .
NATURE IMMUNOLOGY, 2001, 2 (04) :316-324
[7]   The B cell SH2/PH domain-containing adaptor Bam32/DAPP1 is required for T cell-independent II antigen responses [J].
Fournier, E ;
Isakoff, SJ ;
Ko, K ;
Cardinale, CJ ;
Inghirami, GG ;
Li, Z ;
de Lafaille, MAC ;
Skolnik, EY .
CURRENT BIOLOGY, 2003, 13 (21) :1858-1866
[8]   Up-regulation of the IKCa1 potassium channel during T-cell activation -: Molecular mechanism and functional consequences [J].
Ghanshani, S ;
Wulff, H ;
Miller, MJ ;
Rohm, H ;
Neben, A ;
Gutman, GA ;
Cahalan, MD ;
Chandy, KG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (47) :37137-37149
[9]   The PI-3 kinase/Akt pathway and T cell activation:: pleiotropic pathways downstream of PIP3 [J].
Kane, LP ;
Weiss, A .
IMMUNOLOGICAL REVIEWS, 2003, 192 (01) :7-20
[10]   Domains responsible for constitutive and Ca2+-dependent interactions between calmodulin and small conductance Ca2+ activated potassium channels [J].
Keen, JE ;
Khawaled, R ;
Farrens, DL ;
Neelands, T ;
Rivard, A ;
Bond, CT ;
Janowsky, A ;
Fakler, B ;
Adelman, JP ;
Maylie, J .
JOURNAL OF NEUROSCIENCE, 1999, 19 (20) :8830-8838