特应性皮炎
免疫学
生物
细胞因子
白细胞介素13
上皮
细胞生物学
白细胞介素4
遗传学
作者
Sarah R. Wilson,Lydia Thé,Lyn Batia,Katherine Beattie,George E. Katibah,Shannan P. McClain,Maurizio Pellegrino,Daniel M. Estandian,Diana M. Bautista
出处
期刊:Cell
[Cell Press]
日期:2013-10-01
卷期号:155 (2): 285-295
被引量:965
标识
DOI:10.1016/j.cell.2013.08.057
摘要
Atopic dermatitis (AD) is a chronic itch and inflammatory disorder of the skin that affects one in ten people. Patients suffering from severe AD eventually progress to develop asthma and allergic rhinitis, in a process known as the “atopic march.” Signaling between epithelial cells and innate immune cells via the cytokine thymic stromal lymphopoietin (TSLP) is thought to drive AD and the atopic march. Here, we report that epithelial cells directly communicate to cutaneous sensory neurons via TSLP to promote itch. We identify the ORAI1/NFAT calcium signaling pathway as an essential regulator of TSLP release from keratinocytes, the primary epithelial cells of the skin. TSLP then acts directly on a subset of TRPA1-positive sensory neurons to trigger robust itch behaviors. Our results support a model whereby calcium-dependent TSLP release by keratinocytes activates both primary afferent neurons and immune cells to promote inflammatory responses in the skin and airways.
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