Transcriptional Regulation of Mouse Mast Cell Differentiation and the Role of Human Lung Mast Cells in Airway Inflammation

被引:0
作者
Gao, Junfeng [1 ]
Zhao, Dianzheng [1 ]
Nouri, Hamid Reza [2 ]
Chu, Hong Wei [2 ]
Huang, Hua [1 ,3 ]
机构
[1] Natl Jewish Hlth, Dept Immunol & Genom Med, Denver, CO 80206 USA
[2] Natl Jewish Hlth, Dept Med, Denver, CO USA
[3] Univ Colorado Anschutz Med Campus, Dept Immunol & Microbiol, Aurora, CO 80045 USA
基金
美国国家卫生研究院;
关键词
enhancers; lung inflammation; mast cell genes; mast cell progenitors; transcription factors; transcriptional cooperation; FC-EPSILON-RI; ACTIVATOR PROTEIN-1; SUPER-ENHANCERS; CUTTING EDGE; BONE-MARROW; C/EBP-ALPHA; TH2; CELLS; KAPPA-B; EXPRESSION; BASOPHIL;
D O I
10.1111/imr.70026
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mast cells (MCs) play a critical role in allergic inflammation, anaphylaxis, and chronic inflammatory diseases such as asthma, COPD, and osteoarthritis. Dysregulated MC activation can lead to MC activation syndrome (MACS), which is observed in patients with long COVID. MCs express the high-affinity receptor for IgE and, upon activation, release mediators and cytokines that trigger anaphylactic shock and promote allergic inflammation. They also interact with epithelial and nerve cells, which are crucial in forming a complex network of cell-cell and gene-gene interactions driving chronic inflammation that can confer resistance to treatment. In this review, in the context of the literature, we focus on experiments conducted in our laboratory investigating how transcription factors and enhancers regulate genes critical in mouse MC differentiation and function related to human lung inflammation.
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页数:14
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