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Rab5 regulates the kiss and run fusion between phagosomes and endosomes and the acquisition of phagosome leishmanicidal properties in RAW 264.7 macrophages
被引:0
|作者:
Duclos, S
Diez, R
Garin, J
Papadopoulou, B
Descoteaux, A
Stenmark, H
Desjardins, M
机构:
[1] Univ Montreal, Dept Pathol & Biol Cellulaire, Montreal, PQ H3C 3J7, Canada
[2] CEA, Lab Chim Prot, F-38054 Grenoble, France
[3] CHUQ, Ctr Rech Infectiol, St Foy, PQ G1V 4G2, Canada
[4] Univ Quebec, Inst Armand Frappier, INRS, Laval, PQ H7V 1B7, Canada
[5] Norwegian Radium Hosp, Dept Biochem, N-0310 Oslo, Norway
关键词:
Rab5;
phagosome;
kiss and run;
leishmania;
membrane fusion;
D O I:
暂无
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
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.
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页码:3531 / 3541
页数:11
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