IGF-1 promotes the development and cytotoxic activity of human NK cells

被引:90
作者
Ni, Fang [1 ,2 ]
Sun, Rui [1 ]
Fu, Binqing [1 ,3 ]
Wang, Fuyan [1 ]
Guo, Chuang [1 ]
Tian, Zhigang [1 ,3 ]
Wei, Haiming [1 ]
机构
[1] Univ Sci & Technol China, Inst Immunol, Sch Life Sci, Hefei 230027, Anhui, Peoples R China
[2] Anhui Med Univ, Dept Pathophysiol, Hefei 230032, Anhui, Peoples R China
[3] Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
NATURAL-KILLER-CELLS; GROWTH-FACTOR-I; FLOW-CYTOMETRY; T-CELLS; EXPRESSION; RECEPTORS; HORMONE; MICE; LYMPHOCYTE; MICRORNAS;
D O I
10.1038/ncomms2484
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Insulin-like growth factor 1 (IGF-1) is a critical regulator of many physiological functions, ranging from longevity to immunity. However, little is known about the role of IGF-1 in natural killer cell development and function. Here, we identify an essential role for IGF-1 in the positive regulation of human natural killer cell development and cytotoxicity. Specifically, we show that human natural killer cells have the ability to produce IGF-1 and that differential endogenous IGF-1 expression leads to disparate cytotoxicity in human primary natural killer cells. Moreover, miR-483-3p is identified as a critical regulator of IGF-1 expression in natural killer cells. Overexpression of miR-483-3p has an effect similar to IGF-1 blockade and decreased natural killer cell cytotoxicity, whereas inhibition of miR-483-3p has the opposite effect, which is reversible with IGF-1 neutralizing antibody. These findings indicate that IGF-1 and miR-483-3p belong to a new class of natural killer cell functional modulators and strengthen the prominent role of IGF-1 in innate immunity.
引用
收藏
页数:11
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