Calcineurin/NFAT signalling inhibits myeloid haematopoiesis

被引:31
作者
Fric, Jan [1 ]
Lim, Clarice X. F. [1 ]
Koh, Esther G. L. [1 ]
Hofmann, Benjamin [1 ]
Chen, Jinmiao [1 ]
Tay, Hock Soon [1 ]
Isa, Siti Aminah Bte Mohammad [2 ]
Mortellaro, Alessandra [1 ]
Ruedl, Christiane [2 ]
Ricciardi-Castagnoli, Paola [1 ]
机构
[1] ASTAR, Singapore Immunol Network SIgN, Singapore, Singapore
[2] Nanyang Technol Univ, Sch Biol Sci, Singapore, Singapore
关键词
Cyclosporin A; dendritic cell; haematopoiesis; myeloid lineage; NFAT; DENDRITIC-CELL-DEVELOPMENT; ACTIVATED-T-CELLS; GENE-EXPRESSION ANALYSIS; BONE-MARROW; IN-VIVO; TRANSCRIPTION FACTORS; IL-2; PRODUCTION; NUCLEAR-FACTOR; CYCLOSPORINE-A; SELECTIVE ROLE;
D O I
10.1002/emmm.201100207
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Nuclear factor of activated T cells (NFAT) comprises a family of transcription factors that regulate T cell development, activation and differentiation. NFAT signalling can also mediate granulocyte and dendritic cell (DC) activation, but it is unknown whether NFAT influences their development from progenitors. Here, we report a novel role for calcineurin/NFAT signalling as a negative regulator of myeloid haematopoiesis. Reconstituting lethally irradiated mice with haematopoietic stem cells expressing an NFAT-inhibitory peptide resulted in enhanced development of the myeloid compartment. Culturing bone marrow cells in media supplemented with Flt3-L in the presence of the calcineurin/NFAT inhibitor Cyclosporin A increased numbers of differentiated DC. Global gene expression analysis of untreated DC and NFAT-inhibited DC revealed differential expression of transcripts that regulate cell cycle and apoptosis. In conclusion, these results provide evidence that calcineurin/NFAT signalling negatively regulates myeloid lineage development. The finding that inhibition of NFAT enhances myeloid development provides a novel insight into understanding how the treatment with drugs targeting calcineurin/NFAT signalling influence the homeostasis of the innate immune system.
引用
收藏
页码:269 / 282
页数:14
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