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Implications of silver nanoparticles for H. pylori infection: modulation of CagA function and signaling.
Hochvaldova, Lucie; Posselt, Gernot; Wessler, Silja; Kvítek, Libor; Panácek, Ales.
Afiliação
  • Hochvaldova L; Department of Physical Chemistry, Palacky University Olomouc, Olomouc, Czechia.
  • Posselt G; Department of Biosciences and Medical Biology, Paris Lodron University of Salzburg, Salzburg, Austria.
  • Wessler S; Cancer Cluster Salzburg (CCS), Salzburg, Austria.
  • Kvítek L; Center for Tumor Biology and Immunology (CTBI), Paris Lodron University of Salzburg, Salzburg, Austria.
  • Panácek A; Department of Biosciences and Medical Biology, Paris Lodron University of Salzburg, Salzburg, Austria.
Front Cell Infect Microbiol ; 14: 1419568, 2024.
Article em En | MEDLINE | ID: mdl-38983115
ABSTRACT

Background:

Helicobacter pylori infection poses a significant health burden worldwide, and its virulence factor CagA plays a pivotal role in its pathogenesis.

Methods:

In this study, the interaction between H. pylori-infected AGS cells and silver nanoparticles (AgNPs) was investigated, with a focus on the modulation of CagA-mediated responses, investigated by western blotting. Both, the dose-dependent efficacy against H. pylori (growth curves, CFU assay) and the impact of the nanoparticles on AGS cells (MTT assay) were elucidated.

Results:

AGS cells infected with H. pylori displayed dramatic morphological changes, characterized by elongation and a migratory phenotype, attributed to CagA activity. Preincubation of H. pylori with AgNPs affected these morphological changes in a concentration-dependent manner, suggesting a correlation between AgNPs concentration and CagA function.

Conclusion:

Our study highlights the nuanced interplay between host-pathogen interactions and the therapeutic potential of AgNPs in combating H. pylori infection and offers valuable insights into the multifaceted dynamics of CagA mediated responses.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article