Selected lipids activate phagosome actin assembly and maturation resulting in killing of pathogenic mycobacteria

被引:213
作者
Anes, E
Kühnel, MP
Bos, E
Moniz-Pereira, J
Habermann, A
Griffiths, G
机构
[1] European Mol Biol Lab, D-69117 Heidelberg, Germany
[2] Univ Lisbon, Fac Pharm, Mol Pathogenesis Ctr, P-1600085 Lisbon, Portugal
关键词
D O I
10.1038/ncb1036
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:793 / 802
页数:10
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