Intracellular Heliclobacter pylori in gastric epithelial progenitors

被引:86
|
作者
Oh, JD
Karam, SM
Gordon, JI [1 ]
机构
[1] Washington Univ, Sch Med, Ctr Genome Sci, St Louis, MO 63108 USA
[2] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63108 USA
[3] United Arab Emirates Univ, Dept Anat, Fac Med & Hlth Sci, Al Ain 17666, U Arab Emirates
关键词
adult mammalian epithelial progenitors; bacterial pathogenesis; intracellular bacterial communities; gnotobiotic mice; chronic atrophic gastritis;
D O I
10.1073/pnas.0407657102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Helicobacter pylori is generally viewed as an extracellular pathogen. We have analyzed the tropism of H. pylori clinical isolates in a gnotobiotic transgenic mouse model of human chronic atrophic gastritis, a preneoplastic condition. These mice lack acid-producing parietal cells and have an amplified population of dividing gastric epithelial progenitors (GEPs) that express NeuAc alpha 2,3Gal beta 1,4-glycans recognized by H. pylori adhesins. Scanning confocal and transmission electron microscopic studies of stomachs that had been colonized for 1 month or 1 year revealed intracellular bacterial collections (IBCs) in a small subset of multi- and oligopotential epithelial progenitors. Transmission electron microscopic and multilabel immunohistochemical analyses disclosed bacteria with several morphotypes, including spiral-shaped, in the cytoplasm and endosomes. Several stages in IBC evolution were documented, from a few solitary bacteria to consolidated populations in dividing and nondividing GEPs, to microorganisms traversing breaches in the GEP plasma cell membrane. IBC formation was not a unique feature of H. pylori strains isolated from patients with chronic atrophic gastritis. The notion that adult mammalian epithelial progenitors can function as a repository for H. pylori broadens the view of host habitats available to this and perhaps other pathogens.
引用
收藏
页码:5186 / 5191
页数:6
相关论文
共 50 条
  • [41] Suppression of gastric epithelial and fibroblast restoration by H-pylori
    Samanta, A
    Chen, T
    Kumar, V
    Anandarangam, G
    Marquise, L
    Smith, SM
    GUT, 1997, 41 : A30 - A30
  • [42] Helicobacter pylori CagA: A Critical Destroyer of the Gastric Epithelial Barrier
    Wu, Jia
    Xu, Song
    Zhu, Yongliang
    DIGESTIVE DISEASES AND SCIENCES, 2013, 58 (07) : 1830 - 1837
  • [43] MicroRNA alteration in the Helicobacter pylori infected gastric epithelial cells
    Kim, S. S.
    Kim, C. W.
    Chang, Y. J.
    Byun, S. W.
    Kim, J. K.
    JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2011, 26 : 285 - 285
  • [44] Effects of Helicobacter pylori on biological characteristics of gastric epithelial cells
    Wang, Ping
    Mei, Juan
    Tao, Jing
    Zhang, Ning
    Tian, Hua
    Fu, Guo-Hui
    HISTOLOGY AND HISTOPATHOLOGY, 2012, 27 (08) : 1079 - 1091
  • [45] Alterations in Helicobacter pylori triggered by contact with gastric epithelial cells
    Johnson, Elizabeth M.
    Gaddy, Jennifer A.
    Cover, Timothy L.
    FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2012, 2
  • [46] Helicobacter pylori infection and gastric mucosal epithelial cell apoptosis
    Olivares, D
    Gisbert, JP
    Pajares, JM
    REVISTA ESPANOLA DE ENFERMEDADES DIGESTIVAS, 2005, 97 (07) : 505 - 514
  • [47] Helicobacter pylori CagA: A Critical Destroyer of the Gastric Epithelial Barrier
    Jia Wu
    Song Xu
    Yongliang Zhu
    Digestive Diseases and Sciences, 2013, 58 : 1830 - 1837
  • [48] The carcinogenic effect of H-pylori on the gastric epithelial cell
    Moss, SF
    JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1999, 50 (05): : 847 - 856
  • [49] Effects of Helicobacter pylori on proliferation of gastric epithelial cells in vitro
    Smoot, DT
    Wynn, Z
    Elliott, TB
    Allen, CR
    Mekasha, G
    Naab, T
    Ashktorab, H
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 1999, 94 (06): : 1508 - 1511
  • [50] EPITHELIAL DAMAGE BY HELICOBACTER-PYLORI IN GASTRIC-ULCERS
    CHAN, WY
    HUI, PK
    CHAN, JKC
    CHEUNG, PSY
    NG, CS
    SHAM, CH
    GWI, E
    HISTOPATHOLOGY, 1991, 19 (01) : 47 - 53