胞饮病
脂筏
细胞内
布鲁氏菌
生物
细胞生物学
膜皱折
细胞内寄生虫
巨噬细胞
跨膜蛋白
木筏
微生物学
细胞
生物化学
内吞作用
信号转导
免疫学
化学
受体
细胞骨架
布鲁氏菌病
聚合物
体外
有机化学
共聚物
作者
Masahisa Watarai,Sou-ichi Makino,Yoshio Fujii,Keinosuke Okamoto,Toshikazu Shirahata
标识
DOI:10.1046/j.1462-5822.2002.00195.x
摘要
Intracellular replication of Brucella requires the VirB complex, which is highly similar to conjugative DNA transfer systems. In this study, we show that Brucella internalizes into macrophages by swimming on the cell surface with generalized membrane ruffling for several minutes, after which the bacteria are enclosed by macropinosomes. Lipid raft-associated molecules such as glycosylphosphatidylinositol (GPI)-anchored proteins, GM1 gangliosides and cholesterol were selectively incorporated into macropinosomes containing Brucella. In contrast, lysosomal glycoprotein LAMP-1 and host cell transmembrane protein CD44 were excluded from the macropinosomes. Removing GPI-anchored proteins from the macrophage surface and cholesterol sequestration markedly inhibited the VirB-dependent macropinocytosis and intracellular replication. Our results suggest that the entry route of Brucella into the macrophage determines the intracellular fate of the bacteria that is modulated by lipid raft microdomains.
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