The Epithelial Cell-derived Atopic Dermatitis Cytokine TSLP Activates Neurons to Induce Itch
By Sarah R. Wilson, Lydia Thé, Lyn M. Batia, Katherine Beattie, George E. Katibah, Shannan P. McClain, M. Pellegrino, Daniel Estandian, D. Bautista. Cell, 2013
892 citations recorded by the source corpus.
Summary 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 new 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.
View Paper: https://www.semanticscholar.org/paper/0706723a0767f40db4af786464748117e3e9cd49
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Citations in the corpus
- Interleukins (from IL-1 to IL-38), interferons, transforming growth factor β, and TNF-α: Receptors, functions, and roles in diseases. (2016, background): “TSLP is also associated with atopic dermatitis.(151) Aside from its role in allergic inflammation, TSLP has been implicated to play a role in CRSwith nasal polyps, idiopathic pulmonary fibrosis, primary spontaneous pneumothorax, breast cancer, pancreatic cancer, cervical cancer, and lung cancer.”