Karaffová Viera, Teleky Jana, Pintarič Maša, Langerholc Tomaž, Mudroňová Dagmar, Hudec Erik, Ševčíková Zuzana
Department of Morphological Disciplines, University of Veterinary Medicine and Pharmacy in Košice, Komenského 73, 04181 Košice, Slovakia.
Department of Microbiology, Biochemistry, Molecular Biology and Biotechnology, Faculty of Agriculture and Life Sciences, University of Maribor, Pivola 10, 2311 Hoče, Slovenia.
Life (Basel). 2023 Apr 27;13(5):1090. doi: 10.3390/life13051090.
In our previous studies, B1/1, which was renamed (), was able to modulate the production of pro-inflammatory cytokines and other components of the innate immune response in vitro and in vivo. In this study, we evaluated the effect of B1/1 in two concentrations (1 × 10 and 1 × 10 CFU) on the metabolic activity, adherence ability and relative gene expression of pro-inflammatory interleukins (IL-1β, IL-6, IL-8, IL-18), lumican and olfactomedin 4 produced by non-carcinogenic porcine-derived enterocytes (CLAB). CLAB cells were cultured in a 12-well cell culture plate at a concentration of 4 × 10 cells/well in DMEM medium in a controlled humidified atmosphere for 48 h. A 1 mL volume of each probiotic bacterial suspension was added to the CLAB cells. Plates were incubated for 2 h and 4 h. Our results revealed that B1/1 was able to adhere to CLAB cells in sufficient numbers in both concentrations. In particular, the concentration of 10 B1/1 allowed to modulate the gene expression of pro-inflammatory cytokines, as well as to increase the metabolic activity of the cells. In addition, administration of B1/1 in both concentrations significantly stimulated gene expression for both proteins in the CLAB cell line after 4 h of incubation.
在我们之前的研究中,曾被重新命名为()的B1/1能够在体外和体内调节促炎细胞因子的产生以及先天免疫反应的其他成分。在本研究中,我们评估了两种浓度(1×10和1×10 CFU)的B1/1对非致癌猪源肠细胞(CLAB)产生的促炎白细胞介素(IL-1β、IL-6、IL-8、IL-18)、核纤连蛋白和嗅觉介质4的代谢活性、黏附能力及相关基因表达的影响。CLAB细胞以4×10个细胞/孔的浓度接种于12孔细胞培养板中,在含DMEM培养基的可控湿度环境中培养48小时。向CLAB细胞中加入1 mL每种益生菌细菌悬液。培养板孵育2小时和4小时。我们的结果显示,两种浓度的B1/1都能以足够数量黏附于CLAB细胞。特别是,10浓度的B1/1能够调节促炎细胞因子的基因表达,并提高细胞的代谢活性。此外,孵育4小时后,两种浓度的B1/1给药均显著刺激了CLAB细胞系中这两种蛋白质的基因表达。