Porphyromonas gingivalis Outer Membrane Vesicles Enter Human Epithelial Cells via an Endocytic Pathway and Are Sorted to Lysosomal Compartments

被引:113
作者
Furuta, Nobumichi [1 ]
Tsuda, Kayoko [1 ]
Omori, Hiroko [2 ]
Yoshimori, Tamotsu [2 ]
Yoshimura, Fuminobu [3 ]
Amano, Atsuo [1 ]
机构
[1] Osaka Univ, Grad Sch Dent, Dept Oral Frontier Biol, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Div Cellular & Mol Biol, Dept Cellular Regulat, Microbial Dis Res Inst, Suita, Osaka 5650871, Japan
[3] Aichi Gakuin Univ, Sch Dent, Dept Microbiol, Nagoya, Aichi 464, Japan
关键词
GPI-ANCHORED PROTEINS; MICROBIAL PATHOGENESIS; BACTEROIDES-GINGIVALIS; PINOCYTIC PATHWAY; CDC42; ACTIVATION; FIMBRIAE; COMPLEX; GENE; CHOLESTEROL; AGGREGATION;
D O I
10.1128/IAI.00009-09
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Porphyromonas gingivalis, a periodontal pathogen, secretes outer membrane vesicles (MVs) that contain major virulence factors, including major fimbriae and proteases termed gingipains, although it is not confirmed whether MVs enter host cells. In this study, we analyzed the mechanisms involved in the interactions of P. gingivalis MVs with human epithelial cells. Our results showed that MVs swiftly adhered to HeLa and immortalized human gingival epithelial cells in a fimbria-dependent manner and then entered via a lipid raft-dependent endocytic pathway. The intracellular MVs were subsequently routed to early endosome antigen 1-associated compartments and then were sorted to lysosomal compartments within 90 min, suggesting that intracellular MVs were ultimately degraded by the cellular digestive machinery. However, P. gingivalis MVs remained there for over 24 h and significantly induced acidified compartment formation after being taken up by the cellular digestive machinery. In addition, MV entry was shown to be mediated by a novel pathway for transmission of bacterial products into host cells, a Rac1-regulated pinocytic pathway that is independent of caveolin, dynamin, and clathrin. Our findings indicate that P. gingivalis MVs efficiently enter host cells via an endocytic pathway and survive within the endocyte organelles for an extended period, which provides better understanding of the role of MVs in the etiology of periodontitis.
引用
收藏
页码:4187 / 4196
页数:10
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