LPHI, Université de Montpellier, CNRS, INSERM, Montpellier, France.
ICFO - Institute of Photonic Sciences, The Barcelona Institute of Science and Technology, Castelldefels, Barcelona, Spain.
Elife. 2024 Jan 15;13:e89828. doi: 10.7554/eLife.89828.
Numerous intracellular bacterial pathogens interfere with macrophage function, including macrophage polarization, to establish a niche and persist. However, the spatiotemporal dynamics of macrophage polarization during infection within host remain to be investigated. Here, we implement a model of persistent Typhimurium infection in zebrafish, which allows visualization of polarized macrophages and bacteria in real time at high resolution. While macrophages polarize toward M1-like phenotype to control early infection, during later stages, persists inside non-inflammatory clustered macrophages. Transcriptomic profiling of macrophages showed a highly dynamic signature during infection characterized by a switch from pro-inflammatory to anti-inflammatory/pro-regenerative status and revealed a shift in adhesion program. In agreement with this specific adhesion signature, macrophage trajectory tracking identifies motionless macrophages as a permissive niche for persistent . Our results demonstrate that zebrafish model provides a unique platform to explore, in a whole organism, the versatile nature of macrophage functional programs during bacterial acute and persistent infections.
许多细胞内细菌病原体干扰巨噬细胞的功能,包括巨噬细胞极化,以建立小生境并持续存在。然而,宿主内感染期间巨噬细胞极化的时空动态仍有待研究。在这里,我们在斑马鱼中实施了一种持续感染的模型,该模型允许实时高分辨率可视化极化的巨噬细胞和细菌。虽然巨噬细胞向 M1 样表型极化以控制早期感染,但在后期阶段, 会在非炎症性聚集的巨噬细胞内持续存在。巨噬细胞的转录组谱分析显示,感染过程中存在一个高度动态的特征,其特征是从促炎状态向抗炎/再生状态的转变,并揭示了黏附程序的转变。与这种特定的黏附特征一致,巨噬细胞轨迹跟踪将静止的巨噬细胞鉴定为 持续存在的许可小生境。我们的研究结果表明,斑马鱼模型为在整个生物体中探索巨噬细胞功能程序在细菌急性和持续感染期间的多功能性提供了一个独特的平台。