4.8 Article

The Enzyme Cyp26b1 Mediates Inhibition of Mast Cell Activation by Fibroblasts to Maintain Skin-Barrier Homeostasis

期刊

IMMUNITY
卷 40, 期 4, 页码 530-541

出版社

CELL PRESS
DOI: 10.1016/j.immuni.2014.01.014

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资金

  1. Ministry of Education, Science, Sports, and Technology of Japan
  2. Ministry of Education, Science, Sports, and Technology of Japan grant from Leading-edge Research Infrastructure Program
  3. Young Researcher Overseas Visits Program for Vitalizing Brain Circulation (Japan Society for the Promotion of Science)
  4. Ministry of Health and Welfare of Japan
  5. Global Center of Excellence Program of the Center of Education and Research for Advanced Genome-based Medicine
  6. Program for Promotion of Basic and Applied Research for Innovations in Bio-oriented Industry
  7. Kowa Life Science Foundation
  8. Kishimoto Foundation Research Grant
  9. Yakult Bioscience Foundation
  10. Grants-in-Aid for Scientific Research [24659217, 25116706, 26893047, 26293111, 11J04859, 26670241] Funding Source: KAKEN

向作者/读者索取更多资源

Mast 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.

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