Xin Yan, Xiong Sihan, Zhou Linghong, Lin Xin
Institute for Immunology and School of Medicine, Tsinghua University, 100084, Beijing, China.
Tsinghua University-Peking University Center for Life Sciences, 100084, Beijing, China.
Cell Mol Immunol. 2024 Mar;21(3):245-259. doi: 10.1038/s41423-024-01130-4. Epub 2024 Jan 31.
Invasive fungal infections are life-threatening, and neutrophils are vital cells of the innate immune system that defend against them. The role of LTA4H-LTB-BLT1 axis in regulation of neutrophil responses to fungal infection remains poorly understood. Here, we demonstrated that the LTA4H-LTB-BLT1 axis protects the host against Candida albicans and Aspergillus fumigatus, but not Cryptococcus neoformans infection, by regulating the antifungal activity of neutrophils. Our results show that deleting Lta4h or Blt1 substantially impairs the fungal-specific phagocytic capacity of neutrophils. Moreover, defective activation of the spleen tyrosine kinase (Syk) and extracellular signal-related kinase (ERK1/2) pathways in neutrophils accompanies this impairment. Mechanistically, BLT1 regulates CR3-mediated, β-1,3-glucan-induced neutrophil phagocytosis, while a physical interaction with CR3 with slight influence on its dynamics is observed. Our findings thus demonstrate that the LTA4H-LTB-BLT1 axis is essential for the phagocytic function of neutrophils in host antifungal immune response against Candida albicans and Aspergillus fumigatus.
侵袭性真菌感染会危及生命,而中性粒细胞是抵御此类感染的固有免疫系统的重要细胞。LTA4H-LTB-BLT1轴在调节中性粒细胞对真菌感染的反应中的作用仍知之甚少。在此,我们证明LTA4H-LTB-BLT1轴通过调节中性粒细胞的抗真菌活性来保护宿主抵御白色念珠菌和烟曲霉感染,但对新型隐球菌感染无效。我们的结果表明,敲除Lta4h或Blt1会显著损害中性粒细胞的真菌特异性吞噬能力。此外,中性粒细胞中脾酪氨酸激酶(Syk)和细胞外信号调节激酶(ERK1/2)通路的激活缺陷伴随着这种损害。从机制上讲,BLT1调节CR3介导的、β-1,3-葡聚糖诱导的中性粒细胞吞噬作用,同时观察到其与CR3存在物理相互作用,对其动力学有轻微影响。因此,我们的研究结果表明,LTA4H-LTB-BLT1轴对于宿主抗白色念珠菌和烟曲霉的抗真菌免疫反应中中性粒细胞的吞噬功能至关重要。