Replication Stress in Activated Human NK Cells Induces Sensitivity to Apoptosis

被引:1
|
作者
Guilz, Nicole C. [1 ]
Ahn, Yong-Oon [1 ]
Fatima, Hijab [1 ]
Pedroza, Luis Alberto [1 ]
Seo, Seungmae [1 ]
Soni, Rajesh Kumar [2 ]
Wang, Ning [3 ]
Egli, Dieter [3 ]
Mace, Emily M. [1 ]
机构
[1] Columbia Univ, Vagelos Coll Phys & Surg, Dept Pediat, New York, NY USA
[2] Columbia Univ, Herbert Irving Comprehens Canc Ctr, Prote & Macromol Crystallog Shared Resource, New York, NY USA
[3] Columbia Univ, Vagelos Coll Phys & Surg, Naomi Berrie Diabet Ctr, Columbia Stem Cell Initiat,Pediat & Obstet & Gynec, New York, NY USA
来源
JOURNAL OF IMMUNOLOGY | 2024年 / 213卷 / 01期
基金
美国国家卫生研究院;
关键词
GROWTH-RETARDATION; MEMORY; DEFICIENCY; DNA; ORIGINS; BIOLOGY; HEALTH;
D O I
10.4049/jimmunol.2300843
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
NK cells are innate immune effectors that kill virally infected or malignant cells. NK cell deficiency (NKD) occurs when NK cell development or function is impaired and variants in MCM4, , GINS1, , MCM10, , and GINS4 result in NKD. Although NK cells are strongly impacted by mutational deficiencies in helicase proteins, the mechanisms underlying this specific susceptibility are poorly understood. In this study, we induced replication stress in activated NK cells or T cells by chemical and genetic methods. We found that the CD56 bright subset of NK cells accumulates more DNA damage and replication stress during activation than do CD56dim dim NK cells or T cells. Aphidicolin treatment increases apoptosis of CD56 bright NK cells through increased pan-caspase expression and decreases perforin expression in surviving cells. These findings show that sensitivity to replication stress affects NK cell survival and function and contributes to NKD. The Journal of Immunology, , 2024, 213: 40-51.- 51.
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页数:13
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