Anes Elsa, Kühnel Mark Philipp, Bos Evelyne, Moniz-Pereira Jose, Habermann Anja, Griffiths Gareth
Molecular Pathogenesis Centre, Faculty of Pharmacy, University of Lisbon, Av. Forcas Armadas, 1600-085 Lisbon, Portugal.
Nat Cell Biol. 2003 Sep;5(9):793-802. doi: 10.1038/ncb1036. Epub 2003 Aug 24.
Pathogenic mycobacteria such as Mycobacterium tuberculosis and Mycobacterium avium facilitate disease by surviving intracellularly within a potentially hostile environment: the macrophage phagosome. They inhibit phagosome maturation processes, including fusion with lysosomes, acidification and, as shown here, membrane actin assembly. An in vitro assay developed for latex bead phagosomes (LBPs) provided insights into membrane signalling events that regulate phagosome actin assembly, a process linked to membrane fusion. Different lipids were found to stimulate or inhibit actin assembly by LBPs and mycobacterial phagosomes in vitro. In addition, selected lipids activated actin assembly and phagosome maturation in infected macrophages, resulting in a significant killing of M. tuberculosis and M. avium. In contrast, the polyunsaturated sigma-3 lipids behaved differently and stimulated pathogen growth. Thus, lipids can be involved in both stimulatory and inhibitory signalling networks in the phagosomal membrane.
致病性分枝杆菌,如结核分枝杆菌和鸟分枝杆菌,通过在潜在的恶劣环境——巨噬细胞吞噬体内存活来引发疾病。它们抑制吞噬体成熟过程,包括与溶酶体融合、酸化,以及如本文所示的膜肌动蛋白组装。为乳胶珠吞噬体(LBP)开发的体外检测方法,为调节吞噬体肌动蛋白组装的膜信号事件提供了见解,这一过程与膜融合相关。发现不同的脂质在体外可刺激或抑制LBP和分枝杆菌吞噬体的肌动蛋白组装。此外,特定脂质可激活感染巨噬细胞中的肌动蛋白组装和吞噬体成熟,从而显著杀死结核分枝杆菌和鸟分枝杆菌。相比之下,多不饱和sigma-3脂质表现不同,会刺激病原体生长。因此,脂质可参与吞噬体膜中的刺激和抑制信号网络。