The IL-15-AKT-XBP1s signaling pathway contributes to effector functions and survival in human NK cells

被引:88
作者
Wang, Yufeng [1 ,2 ]
Zhang, Yibo [1 ]
Yi, Ping [1 ,3 ]
Dong, Wenjuan [1 ,4 ]
Nalin, Ansel P. [1 ,5 ]
Zhang, Jianying [6 ]
Zhu, Zheng [1 ,4 ]
Chen, Lichao [1 ]
Benson, Don M. [1 ,2 ]
Mundy-Bosse, Bethany L. [1 ,2 ]
Freud, Aharon G. [1 ,7 ]
Caligiuri, Michael A. [4 ,8 ]
Yu, Jianhua [1 ,2 ,4 ,8 ]
机构
[1] Ohio State Univ, Comprehens Canc Ctr, Columbus, OH 43210 USA
[2] Ohio State Univ, Dept Internal Med, Div Hematol, Columbus, OH 43210 USA
[3] Third Mil Med Univ, Affiliated Hosp 3, Chongqing, Peoples R China
[4] City Hope Natl Med Ctr, Dept Hematol & Hematopoiet Cell Transplant, 1500 E Duarte Rd, Duarte, CA 91010 USA
[5] Ohio State Univ, Med Scientist Training Program, Columbus, OH 43210 USA
[6] City Hope Natl Med Ctr, Dept Informat Sci, Div Biostat, 1500 E Duarte Rd, Duarte, CA 91010 USA
[7] Ohio State Univ, Dept Pathol, Columbus, OH 43210 USA
[8] City Hope Natl Med Ctr, Hematol Malignancies & Stem Cell Transplantat Ins, 1500 E Duarte Rd, Duarte, CA 91010 USA
基金
美国国家卫生研究院;
关键词
ENDOPLASMIC-RETICULUM STRESS; NATURAL-KILLER-CELLS; TERMINAL MATURATION; PROTEIN-SYNTHESIS; XBP1; INTERLEUKIN-15; P110-DELTA; EXPRESSION; REGULATOR; DIFFERENTIATION;
D O I
10.1038/s41590-018-0265-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interleukin 15 (IL-15) is one of the most important cytokines that regulate the biology of natural killer (NK) cells(1). Here we identified a signaling pathway-involving the serine-threonine kinase AKT and the transcription factor XBP1s, which regulates unfolded protein response genes(2,3)-that was activated in response to IL-15 in human NK cells. IL-15 induced the phosphorylation of AKT, which led to the deubiquitination, increased stability and nuclear accumulation of XBP1s protein. XBP1s bound to and recruited the transcription factor T-BET to the gene encoding granzyme B, leading to increased transcription. XBP1s positively regulated the cytolytic activity of NK cells against leukemia cells and was also required for IL-15-mediated NK cell survival through an anti-apoptotic mechanism. Thus, the newly identified IL-15-AKT-XBP1s signaling pathway contributes to enhanced effector functions and survival of human NK cells.
引用
收藏
页码:10 / +
页数:9
相关论文
共 46 条
[31]   XBP1 is essential for survival under hypoxic conditions and is required for tumor growth [J].
Romero-Ramirez, L ;
Cao, HB ;
Nelson, D ;
Hammond, E ;
Lee, AH ;
Yoshida, H ;
Mori, K ;
Glimcher, LH ;
Denko, NC ;
Giaccia, AJ ;
Le, QT ;
Koong, AC .
CANCER RESEARCH, 2004, 64 (17) :5943-5947
[32]   XBP1, downstream of Blimp-1, expands the secretory apparatus and other organelles, and increases protein synthesis in plasma cell differentiation [J].
Shaffer, AL ;
Shapiro-Shelef, M ;
Iwakoshi, NN ;
Lee, AH ;
Qian, SB ;
Zhao, H ;
Yu, X ;
Yang, LM ;
Tan, BK ;
Rosenwald, A ;
Hurt, EM ;
Petroulakis, E ;
Sonenberg, N ;
Yewdell, JW ;
Calame, K ;
Glimcher, LH ;
Staudt, LM .
IMMUNITY, 2004, 21 (01) :81-93
[33]   p110γ and p110δ phosphoinositide 3-kinase signaling pathways synergize to control development and functions of murine NK cells [J].
Tassi, Ilaria ;
Cella, Marina ;
Gilfillan, Susan ;
Turnbull, Isaiah ;
Diacovo, Thomas G. ;
Penninger, Josef M. ;
Colonna, Marco .
IMMUNITY, 2007, 27 (02) :214-227
[34]   T-bet regulates the terminal maturation and homeostasis of NK and Vα14i NKT cells [J].
Townsend, MJ ;
Weinmann, AS ;
Matsuda, JL ;
Salomon, R ;
Farnham, PJ ;
Biron, CA ;
Gapin, L ;
Glimcher, LH .
IMMUNITY, 2004, 20 (04) :477-494
[35]   Unconventional splicing of XBP1 mRNA occurs in the cytoplasm during the mammalian unfolded protein response [J].
Uemura, Aya ;
Oku, Masaya ;
Mori, Kazutoshi ;
Yoshida, Hiderou .
JOURNAL OF CELL SCIENCE, 2009, 122 (16) :2877-2886
[36]   STAT5-mediated signals sustain a TCR-initiated gene expression program toward differentiation of CD8 T cell effectors [J].
Verdeil, Gregory ;
Puthier, Denis ;
Nguyen, Catherine ;
Schmitt-Verhulst, Anne-Marie ;
Auphan-Anezin, Nathalie .
JOURNAL OF IMMUNOLOGY, 2006, 176 (08) :4834-4842
[37]   Cell cycle progression dictates the requirement for BCL2 in natural killer cell survival [J].
Viant, Charlotte ;
Guia, Sophie ;
Hennessy, Robert J. ;
Rautela, Jai ;
Pham, Kim ;
Bernat, Claire ;
Goh, Wilford ;
Jiao, Yuhao ;
Delconte, Rebecca ;
Roger, Michael ;
Simon, Vanina ;
Souza-Fonseca-Guimaraes, Fernando ;
Grabow, Stephanie ;
Belz, Gabrielle T. ;
Kile, Benjamin T. ;
Strasser, Andreas ;
Gray, Daniel ;
Hodgkin, Phillip D. ;
Beutler, Bruce ;
Vivier, Eric ;
Ugolini, Sophie ;
Huntington, Nicholas D. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2017, 214 (02) :491-510
[38]   Unspliced XBP1 controls autophagy through FoxO1 [J].
Vidal, Rene L. ;
Hetz, Claudio .
CELL RESEARCH, 2013, 23 (04) :463-464
[39]   PI3K inhibitor LY294002, as opposed to wortmannin, enhances AKT phosphorylation in gemcitabine-resistant pancreatic cancer cells [J].
Wang, Yufeng ;
Kuramitsu, Yasuhiro ;
Baron, Byron ;
Kitagawa, Takao ;
Tokuda, Kazuhiro ;
Akada, Junko ;
Maehara, Shin-Ichiro ;
Maehara, Yoshihiko ;
Nakamura, Kazuyuki .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2017, 50 (02) :606-612
[40]   CGK733-induced LC3 II formation is positively associated with the expression of cyclin-dependent kinase inhibitor p21Waf1/Cip1 through modulation of the AMPK and PERK/CHOP signaling pathways [J].
Wang, Yufeng ;
Kuramitsu, Yasuhiro ;
Baron, Byron ;
Kitagawa, Takao ;
Tokuda, Kazuhiro ;
Akada, Junko ;
Nakamura, Kazuyuki .
ONCOTARGET, 2015, 6 (37) :39692-39701