4.7 Article

NK Cell Recognition of Candida glabrata through Binding of NKp46 and NCR1 to Fungal Ligands Epa1, Epa6, and Epa7

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CELL HOST & MICROBE
卷 20, 期 4, 页码 527-534

出版社

CELL PRESS
DOI: 10.1016/j.chom.2016.09.008

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资金

  1. European Research Council under the European Union's Seventh Framework Programme (FP)/ERC [320473-BacNK]
  2. NIH [5RO1AI046223, GM62116, GM098791]
  3. I-CORE Program of the Planning and Budgeting Committee
  4. Israel Science Foundation
  5. I-Core on Chromatin and RNA in Gene Regulation
  6. GIF foundation
  7. Lewis family foundation
  8. ICRF professorship grant
  9. Helmholtz Israel grant
  10. Rosetrees Trust
  11. Rosetrees Trust [M21-F1] Funding Source: researchfish

向作者/读者索取更多资源

Natural killer (NK) cells form an important arm of the innate immune system and function to combat a wide range of invading pathogens, ranging from viruses to bacteria. However, the means by which NK cells accomplish recognition of pathogens with a limited repertoire of receptors remain largely unknown. In the current study, we describe the recognition of an emerging fungal pathogen, Candida glabrata, by the human NK cytotoxic receptor NKp46 and its mouse ortholog, NCR1. Using NCR1 knockout mice, we observed that this receptor-mediated recognition was crucial for controlling C. glabrata infection in vitro and in vivo. Finally, we delineated the fungal ligands to be the C. glabrata adhesins Epa1, Epa6, and Epa7 and demonstrated that clearance of systemic C. glabrata infections in vivo depends on their recognition by NCR1. As NKp46 and NCR1 have been previously shown to bind viral adhesion receptors, we speculate that NKp46/NCR1 may be a novel type of pattern recognition receptor.

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