Sun Wanwei, Wu Han, Zhao Guimin, Shui Qing, Zhang Lei, Luan Xiaoxi, Chen Tian, Liu Feng, Zheng Yi, Zhao Wei, Qi Xiaopeng, Liu Bingyu, Gao Chengjiang
Key Laboratory of Infection and Immunity of Shandong Province & Key Laboratory for Experimental Teratology of Ministry of Education, Shandong University, Jinan, Shandong, 250012, P. R. China.
Department of Immunology, School of Biomedical Sciences, Shandong University, Jinan, Shandong, 250012, P. R. China.
Cell Mol Immunol. 2025 May;22(5):468-484. doi: 10.1038/s41423-025-01282-x. Epub 2025 Apr 7.
Lipid droplets (LDs) are intracellular organelles that can be induced and interact with phagosomes during the process of pathogen phagocytosis in macrophages. However, the function of LDs in phagocytosis remains elusive. Here, we unveil the role of LDs in modulating phagosome formation via a fungal infection model. Specifically, LD accumulation restricted the degree of phagosome formation and protected macrophages from death. Mechanistically, LD formation competitively consumed the intracellular endoplasmic reticulum membrane and altered RAC1 translocation and GTPase activity, which resulted in limited phagosome formation in macrophages during fungal engulfment. Mice with Hilpda-deficient macrophages were more susceptible to the lethal sequelae of systemic infection with C. albicans. Notably, administration of the ATGL inhibitor atglistatin improved host outcomes in disseminated fungal infections. Taken together, our study elucidates the mechanism by which LDs control phagosome formation to prevent immune cell death and offers a potential drug target for the treatment of C. albicans infections.
脂滴(LDs)是细胞内细胞器,在巨噬细胞病原体吞噬过程中可被诱导并与吞噬体相互作用。然而,脂滴在吞噬作用中的功能仍不清楚。在此,我们通过真菌感染模型揭示了脂滴在调节吞噬体形成中的作用。具体而言,脂滴积累限制了吞噬体形成程度,并保护巨噬细胞免于死亡。机制上,脂滴形成竞争性消耗细胞内内质网膜,并改变RAC1易位和GTP酶活性,这导致巨噬细胞在吞噬真菌期间吞噬体形成受限。巨噬细胞中缺乏Hilpda的小鼠更容易受到白色念珠菌全身感染致死后遗症的影响。值得注意的是,给予ATGL抑制剂atglistatin可改善播散性真菌感染中的宿主结局。综上所述,我们的研究阐明了脂滴控制吞噬体形成以防止免疫细胞死亡的机制,并为治疗白色念珠菌感染提供了一个潜在的药物靶点。