Duclos S, Diez R, Garin J, Papadopoulou B, Descoteaux A, Stenmark H, Desjardins M
Département de pathologie et biologie cellulaire, Université de Montréal, C.P. 6128, Succ. Centre ville, Montréal, QC, Canada, H3C 3J7.
J Cell Sci. 2000 Oct;113 Pt 19:3531-41. doi: 10.1242/jcs.113.19.3531.
Phagolysosome biogenesis is essential for the killing and degradation of intracellular pathogens. It involves the fusion of phagosomes with various endocytic organelles, a process known to be regulated in part by Rab proteins. We generated RAW 264.7 macrophages expressing an active mutant of Rab5 (Rab5(Q79L)) to determine the role of Rab5 in phagocytosis and phagolysosome biogenesis. Our results indicate that Rab5 stimulates phagocytosis of latex beads but not Fc or C3 receptor-mediated phagocytosis. Rab5 also acts to restrict the complete fusion of phagosomes with endosomes, a phenomenon allowing exchange of solutes from the two compartments without complete intermixing of their membrane (kiss and run). In Rab5(Q79L)-expressing macrophages, uncontrolled fusion events occurred, leading to the appearance of giant phagosomes. These phagosomes could initiate their maturation and acquire LAMP1, but failed to generate the microbicidal conditions needed to kill intracellular parasites. These results identify Rab5 as a key molecule regulating phagosome-endosome fusion and as an essential component in the innate ability of macrophages to restrict the growth of intracellular parasites.
吞噬溶酶体的生物发生对于细胞内病原体的杀伤和降解至关重要。它涉及吞噬体与各种内吞细胞器的融合,这一过程已知部分受Rab蛋白调控。我们构建了表达活性突变型Rab5(Rab5(Q79L))的RAW 264.7巨噬细胞,以确定Rab5在吞噬作用和吞噬溶酶体生物发生中的作用。我们的结果表明,Rab5刺激乳胶珠的吞噬作用,但不刺激Fc或C3受体介导的吞噬作用。Rab5还起到限制吞噬体与内体完全融合的作用,这种现象允许两个区室之间交换溶质而无需其膜完全混合(即“吻别即走”)。在表达Rab5(Q79L)的巨噬细胞中,发生了不受控制的融合事件,导致出现巨大吞噬体。这些吞噬体可以启动其成熟并获得LAMP1,但未能产生杀死细胞内寄生虫所需的杀菌条件。这些结果确定Rab5是调节吞噬体-内体融合的关键分子,也是巨噬细胞限制细胞内寄生虫生长的先天能力的重要组成部分。