烟曲霉
NADPH氧化酶
串扰
STAT1
先天免疫系统
内部收益率3
免疫学
生物
信号转导
微生物学
细胞生物学
免疫系统
活性氧
物理
光学
作者
Yahui Guo,Mariano A. Aufiero,K. Mills,Simon Grassmann,Hyunu Kim,Mergim Gjonbalaj,Paul Zumbo,Audrey Billips,Katrina B. Mar,Xi Yao,Laura Echeverri Tirado,Lena J. Heung,Amariliz Rivera,Doron Betel,Joseph C. Sun,Tobias M. Hohl
摘要
Aspergillus fumigatus is the most common cause of invasive aspergillosis (IA), a devastating infection in immunocompromised patients. Plasmacytoid dendritic cells (pDCs) regulate host defense against IA by enhancing neutrophil antifungal properties in the lung. Here, we define the pDC activation trajectory during A. fumigatus infection and the molecular events that underlie the protective pDC - neutrophil crosstalk. Fungus-induced pDC activation begins after bone marrow egress and results in pDC-dependent regulation of lung type I and type III IFN levels. These pDC-derived products act on type I and type III IFN receptor-expressing neutrophils and control neutrophil fungicidal activity and reactive oxygen species production via STAT1 signaling in a cell-intrinsic manner. Mechanistically, neutrophil STAT1 signaling regulates the transcription and expression of Cybb, which encodes one of five NADPH oxidase subunits. Thus, pDCs regulate neutrophil-dependent immunity against inhaled molds by controlling the local expression of a subunit required for NADPH oxidase assembly and activity in the lung.
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