Expression profiling of constitutive mast cells reveals a unique identity within the immune system

被引:277
作者
Dwyer, Daniel F. [1 ,2 ]
Barrett, Nora A. [1 ,2 ]
Austen, K. Frank [1 ,2 ]
机构
[1] Brigham & Womens Hosp, Div Rheumatol Immunol & Allergy, 75 Francis St, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
基金
美国国家卫生研究院;
关键词
IMMUNOGLOBULIN-E; TRICHINELLA-SPIRALIS; MESSENGER-RNA; MICE; ACTIVATION; BASOPHILS; DIFFERENTIATION; DEFENSE; RELEASE; IDENTIFICATION;
D O I
10.1038/ni.3445
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 are evolutionarily ancient sentinel cells. Like basophils, mast cells express the high-affinity receptor for immunoglobulin E (IgE) and have been linked to host defense and diverse immune-system-mediated diseases. To better characterize the function of these cells, we assessed the transcriptional profiles of mast cells isolated from peripheral connective tissues and basophils isolated from spleen and blood. We found that mast cells were transcriptionally distinct, clustering independently from all other profiled cells, and that mast cells demonstrated considerably greater heterogeneity across tissues than previously appreciated. We observed minimal homology between mast cells and basophils, which shared more overlap with other circulating granulocytes than with mast cells. The derivation of mast-cell and basophil transcriptional signatures underscores their differential capacities to detect environmental signals and influence the inflammatory milieu.
引用
收藏
页码:878 / +
页数:12
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