4.7 Article

Modulation of the fungal mycobiome is regulated by the chitin-binding receptor FIBCD1

期刊

JOURNAL OF EXPERIMENTAL MEDICINE
卷 216, 期 12, 页码 2689-2700

出版社

ROCKEFELLER UNIV PRESS
DOI: 10.1084/jem.20182244

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资金

  1. Novo Nordisk Foundation [14052]
  2. Fonden til laegevidenskabens Fremme [16-248]
  3. HorslevFonden [203866]
  4. Augustinus Fonden [15-1374]
  5. Aage og Johanne Louis-Hansens Fond [L-153, 18-2B-2769]
  6. Civilingenior Frode V Nyegaard og Hustrus Fond
  7. Dagmar Marshalls Fond
  8. Knud Hojgaards Fond [48-780]
  9. Crohn's and Colitis Foundation of America
  10. Jill Roberts Institute
  11. National Institutes of Health [DK113136, AI137157, AI074878, AI095466, AI095608, AI102942]
  12. Burroughs Wellcome Fund
  13. Cure for IBD
  14. Rosanne H. Silbermann Foundation

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Host-microbiota interactions are critical in regulating mammalian health and disease. In addition to bacteria, parasites, and viruses, beneficial communities of fungi (the mycobiome) are important modulators of immune- and tissue-homeostasis. Chitin is a major component of the fungal cell wall, and fibrinogen C containing domain 1 (FIBCD1) is a chitin-binding protein; however, the role of this molecule in influencing host-mycobiome interactions in vivo has never been examined. Here, we identify direct binding of FIBCD1 to intestinal-derived fungi and demonstrate that epithelial-specific expression of FIBCD1 results in significantly reduced fungal colonization and amelioration of fungal-driven intestinal inflammation. Collectively, these results identify FIBCD1 as a previously unrecognized microbial pattern recognition receptor through which intestinal epithelial cells can recognize and control fungal colonization, limit fungal dysbiosis, and dampen intestinal inflammation.

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