MicroRNAs: New regulators of IL-22

被引:9
作者
Lu, Zhou [1 ]
Liu, Ronghua [1 ]
Huang, Enyu [1 ]
Chu, Yiwei [1 ,2 ]
机构
[1] Fudan Univ, Dept Immunol, Sch Basic Med Sci, Shanghai 200032, Peoples R China
[2] Fudan Univ, Biotherapy Res Ctr, Shanghai 200032, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
MicroRNAs; IL-22; Regulators; CD4(+) T-CELLS; ARYL-HYDROCARBON RECEPTOR; INNATE LYMPHOID-CELLS; IL-10; PRODUCTION; INTERLEUKIN; 22; GENE-EXPRESSION; C-MAF; TH17; ACTIVATION; DRIVES;
D O I
10.1016/j.cellimm.2016.05.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Interleukin-22 (IL-22) is a cytokine that belongs to the IL-10 family of interleukins. It can be produced by T helper 22 (Th22) cells, T helper 1 (Th1) cells, T helper 17 (Th17) cells, natural killer 22 (NK22) cells, natural killer T (NKT) cells, innate lymphoid cells (ILCs), and gamma delta T cells. IL-22 acts via binding to a heterodimeric transmembrane receptor complex that consists of IL-22R1 and IL-10R2 and mainly contributes to the tissue repair and host defense. Transcription factors such as retinoid orphan receptor gamma delta (ROR gamma t) and signal transducer and activator of transcription 3 (STAT3), have been reported to play important roles in regulation of IL-22 expression. Recently, it has been demonstrated in several studies that microRNAs (miRNAs) potently regulate expression of interleukins, including production of IL-22. Here, we review current knowledge about regulators of IL-22 expression with a particular emphasis on the role of miRNAs. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 8
页数:8
相关论文
共 86 条
[31]   Interleukin-22 induces hepatic stellate cell senescence and restricts liver fibrosis in mice [J].
Kong, Xiaoni ;
Feng, Dechun ;
Wang, Hua ;
Hong, Feng ;
Bertola, Adeline ;
Wang, Fu-Sheng ;
Gao, Bin .
HEPATOLOGY, 2012, 56 (03) :1150-1159
[32]   AHR drives the development of gut ILC22 cells and postnatal lymphoid tissues via pathways dependent on and independent of Notch [J].
Lee, Jacob S. ;
Cella, Marina ;
McDonald, Keely G. ;
Garlanda, Cecilia ;
Kennedy, Gregory D. ;
Nukaya, Manabu ;
Mantovani, Alberto ;
Kopan, Raphael ;
Bradfield, Christopher A. ;
Newberry, Rodney D. ;
Colonna, Marco .
NATURE IMMUNOLOGY, 2012, 13 (02) :144-U58
[33]   The Crosstalk between IL-22 Signaling and miR-197 in Human Keratinocytes [J].
Lerman, Galya ;
Sharon, Moran ;
Leibowitz-Amit, Raya ;
Sidi, Yechezkel ;
Avni, Dror .
PLOS ONE, 2014, 9 (09)
[34]   Role of interleukin-22 in inflammatory bowel disease [J].
Li, Lin-Jing ;
Gong, Chen ;
Zhao, Mei-Hua ;
Feng, Bai-Sui .
WORLD JOURNAL OF GASTROENTEROLOGY, 2014, 20 (48) :18177-18188
[35]   MiR-568 inhibits the activation and function of CD4+ T cells and Treg cells by targeting NFAT5 [J].
Li, Wei ;
Kong, Ling-bo ;
Li, Jun-Tang ;
Guo, Zhang-Yan ;
Xue, Qian ;
Yang, Tao ;
Meng, Yan-Ling ;
Jin, Bo-Quan ;
Wen, Wei-Hong ;
Yang, An-Gang .
INTERNATIONAL IMMUNOLOGY, 2014, 26 (05) :269-281
[36]  
Li Yanjie, 2015, Zhonghua Xue Ye Xue Za Zhi, V36, P125, DOI 10.3760/cma.j.issn.0253-2727.2015.02.009
[37]   Type I IFN Inhibits Innate IL-10 Production in Macrophages through Histone Deacetylase 11 by Downregulating MicroRNA-145 [J].
Lin, Li ;
Hou, Jin ;
Ma, Feng ;
Wang, Pin ;
Liu, Xingguang ;
Li, Nan ;
Wang, Jianli ;
Wang, Qingqing ;
Cao, Xuetao .
JOURNAL OF IMMUNOLOGY, 2013, 191 (07) :3896-3904
[38]   MicroRNA-98 negatively regulates IL-10 production and endotoxin tolerance in macrophages after LPS stimulation [J].
Liu, Yang ;
Chen, Qingyun ;
Song, Yinjing ;
Lai, Lihua ;
Wang, Jianli ;
Yu, Hai ;
Cao, Xuetao ;
Wang, Qingqing .
FEBS LETTERS, 2011, 585 (12) :1963-1968
[39]   MicroRNA-146a Provides Feedback Regulation of Lyme Arthritis but Not Carditis during Infection with Borrelia burgdorferi [J].
Lochhead, Robert B. ;
Ma, Ying ;
Zachary, James F. ;
Baltimore, David ;
Zhao, Jimmy L. ;
Weis, John H. ;
O'Connell, Ryan M. ;
Weis, Janis J. .
PLOS PATHOGENS, 2014, 10 (06)
[40]   Increased miR-223 expression in T cells from patients with rheumatoid arthritis leads to decreased insulin-like growth factor-1-mediated interleukin-10 production [J].
Lu, M. -C. ;
Yu, C. -L. ;
Chen, H. -C. ;
Yu, H. -C. ;
Huang, H. -B. ;
Lai, N. -S. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2014, 177 (03) :641-651