Anti-inflammatory effects of extracellular vesicles and cell-free supernatant derived from Lactobacillus crispatus strain RIGLD-1 on Helicobacter pylori-induced inflammatory response in gastric epithelial cells in vitro.
Farzaneh FakharianAmir SadeghiFarkhondeh PouresmaeiliNeda SoleimaniAbbas YadegarPublished in: Folia microbiologica (2024)
Helicobacter pylori infection is the major risk factor associated with the development of gastric cancer. Currently, administration of standard antibiotic therapy combined with probiotics and postbiotics has gained significant attention in the management of H. pylori infection. In this work, the immunomodulatory effects of Lactobacillus crispatus-derived extracellular vesicles (EVs) and cell-free supernatant (CFS) were investigated on H. pylori-induced inflammatory response in human gastric adenocarcinoma (AGS) cells. L. crispatus-derived EVs were isolated by ultracentrifugation and physically characterized by dynamic light scattering (DLS), transmission electron microscopy (TEM), and scanning electron microscopy (SEM). Furthermore, the protein content of L. crispatus-derived EVs was also evaluated by SDS-PAGE. Cell viability of AGS cells exposed to varying concentrations of EVs and CFS was assessed by MTT assay. The mRNA expression of IL-1β, IL-6, IL-8, TNF-α, IL-10, and TGF-ß genes was determined by RT-qPCR. ELISA was used for the measurement of IL-8 production in AGS cells. In addition, EVs (50 μg/mL) and CFS modulated the H. pylori-induced inflammation by downregulating the mRNA expression of IL-1β, IL-6, IL-8, and TNF-α, and upregulating the expression of IL-10, and TGF-ß genes in AGS cells. Furthermore, H. pylori-induced IL-8 production was dramatically decreased after treatment with L. crispatus-derived EVs and CFS. In conclusion, our observation suggests for the first time that EVs released by L. crispatus strain RIGLD-1 and its CFS could be recommended as potential therapeutic agents against H. pylori-triggered inflammation.
Keyphrases
- cell free
- helicobacter pylori
- induced apoptosis
- inflammatory response
- helicobacter pylori infection
- electron microscopy
- high glucose
- oxidative stress
- cell cycle arrest
- squamous cell carcinoma
- endothelial cells
- stem cells
- rheumatoid arthritis
- gene expression
- genome wide
- risk factors
- signaling pathway
- dna methylation
- transcription factor
- high throughput
- working memory
- transforming growth factor
- small molecule
- radiation therapy
- high resolution
- circulating tumor cells
- mass spectrometry
- binding protein
- atomic force microscopy
- cell therapy
- pi k akt