炎症体
炎症
斑马鱼
免疫系统
生物
细胞生物学
先天免疫系统
骨髓生成
受体
矽肺
Toll样受体
免疫学
医学
造血
遗传学
基因
病理
干细胞
作者
Sylwia D. Tyrkalska,Annamaria Pedoto,Alicia Martínez‐López,José Antonio Ros,Pablo Mesa-del-Castillo,Sergio Candel,Víctoriano Mulero
标识
DOI:10.1016/j.dci.2022.104523
摘要
Silica crystals are potent activators of the inflammasome that cause a fibrotic lung disease, called silicosis, with no effective treatment available. We report here that injection of silica crystals into the hindbrain ventricle of zebrafish embryos led to the initiation of local and systemic immune responses driven through both Toll-like receptors (TLR)- and inflammasome-dependent signaling pathways, followed by induction of pro-fibrotic markers. Genetic and pharmacological analysis revealed that the Nlrp3 inflammasome regulated silica crystal-induced inflammation and pyroptotic cell death, but not emergency myelopoiesis. In addition, Cxcl8a/Cxcr2-dependent recruitment of myeloid cells to silica crystals was required to promote emergency myelopoiesis and systemic inflammation. The zebrafish model of silicosis developed here shed light onto the molecular mechanisms involved in the activation of the immune system by silica crystals.
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