NKG2D公司
细胞毒性T细胞
细胞内
CD8型
细胞溶解
爱泼斯坦-巴尔病毒
生物
病毒
免疫学
自然杀伤细胞
体外
细胞生物学
免疫系统
生物化学
作者
Benjamin Chaigne-Delalande,Feng-Yen Li,Geraldine M. O’Connor,Marshall J. Lukacs,Ping Jiang,Lixin Zheng,Amber N. Shatzer,Matthew Biancalana,Stefania Pittaluga,Helen Matthews,Timothy Jancel,Jack Bleesing,Rebecca Marsh,Taco W. Kuijpers,Kim E. Nichols,C. Lucas,Sunil Nagpal,Huseyin Mehmet,Helen C. Su,Jeffrey I. Cohen
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2013-07-11
卷期号:341 (6142): 186-191
被引量:340
标识
DOI:10.1126/science.1240094
摘要
The magnesium transporter 1 (MAGT1) is a critical regulator of basal intracellular free magnesium (Mg(2+)) concentrations. Individuals with genetic deficiencies in MAGT1 have high levels of Epstein-Barr virus (EBV) and a predisposition to lymphoma. We show that decreased intracellular free Mg(2+) causes defective expression of the natural killer activating receptor NKG2D in natural killer (NK) and CD8(+) T cells and impairs cytolytic responses against EBV. Notably, magnesium supplementation in MAGT1-deficient patients restores intracellular free Mg(2+) and NKG2D while concurrently reducing EBV-infected cells in vivo, demonstrating a link between NKG2D cytolytic activity and EBV antiviral immunity in humans. Moreover, these findings reveal a specific molecular function of free basal intracellular Mg(2+) in eukaryotic cells.
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