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Get Free AccessMast cells (MCs) mature locally, thus possessing tissue-dependent phenotypes for their critical roles in both protective immunity against pathogens and the development of allergy or inflammation. We previously reported that MCs highly express P2X7, a receptor for extracellular ATP, in the colon but not in the skin. The ATP-P2X7 pathway induces MC activation and consequently exacerbates the inflammation. Here, we identified the mechanisms by which P2X7 expression on MCs is reduced by fibroblasts in the skin, but not in the other tissues. The retinoic-acid-degrading enzyme Cyp26b1 is highly expressed in skin fibroblasts, and its inhibition resulted in the upregulation of P2X7 on MCs. We also noted the increased expression of P2X7 on skin MCs and consequent P2X7- and MC-dependent dermatitis (so-called retinoid dermatitis) in the presence of excessive amounts of retinoic acid. These results demonstrate a unique skin-barrier homeostatic network operating through Cyp26b1-mediated inhibition of ATP-dependent MC activation by fibroblasts.
Yosuke Kurashima, Takeaki Amiya, Kumiko Fujisawa, Naoko Shibata, Yuji Suzuki, Yuta Kogure, Eri Hashimoto, Atsushi Otsuka, Kenji Kabashima, Shintaro Sato, Takeshi Sato, Masato Kubo, Akira Shizuo, Kensuke Miyake, Jun Kunisawa, Hiroshi Kiyono (2014). The Enzyme Cyp26b1 Mediates Inhibition of Mast Cell Activation by Fibroblasts to Maintain Skin-Barrier Homeostasis. Immunity, 40(4), pp. 530-541, DOI: 10.1016/j.immuni.2014.01.014.
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Type
Article
Year
2014
Authors
16
Datasets
0
Total Files
0
Language
English
Journal
Immunity
DOI
10.1016/j.immuni.2014.01.014
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