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<metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/"><dc:title>Application of Lactobacillus reuteri B1/1 (Limosilactobacillus reuteri) improves immunological profile of the non-carcinogenic porcine-derived enterocytes</dc:title><dc:creator>Karaffová,	Viera	(Avtor)
	</dc:creator><dc:creator>Teleky,	Jana	(Avtor)
	</dc:creator><dc:creator>Kozmos,	Maša	(Avtor)
	</dc:creator><dc:creator>Langerholc,	Tomaž	(Avtor)
	</dc:creator><dc:creator>Mudroňová,	Dagmar	(Avtor)
	</dc:creator><dc:creator>Hudec,	Erik	(Avtor)
	</dc:creator><dc:creator>Ševčíková,	Zuzana	(Avtor)
	</dc:creator><dc:subject>Lactobacillus reuteri B1/1</dc:subject><dc:subject>CLAB cells</dc:subject><dc:subject>pro-inflammatory cytokine</dc:subject><dc:subject>metabolic activity</dc:subject><dc:description>In our previous studies, Lactobacillus reuteri B1/1, which was renamed Limosilactobacillus reuteri (L. reuteri), 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 Lactobacillus reuteri B1/1 in two concentrations (1 x 10(7) and 1 x 10(9) CFU) on the metabolic activity, adherence ability and relative gene expression of pro-inflammatory interleukins (IL-1 beta, 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 x 10(5) 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 L. reuteri B1/1 was able to adhere to CLAB cells in sufficient numbers in both concentrations. In particular, the concentration of 109 L. reuteri 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 L. reuteri B1/1 in both concentrations significantly stimulated gene expression for both proteins in the CLAB cell line after 4 h of incubation.</dc:description><dc:publisher>MDPI</dc:publisher><dc:date>2023</dc:date><dc:date>2024-02-20 08:09:38</dc:date><dc:type>Znanstveno delo</dc:type><dc:identifier>87111</dc:identifier><dc:identifier>UDK: 579</dc:identifier><dc:identifier>COBISS_ID: 150715651</dc:identifier><dc:identifier>DOI: 10.3390/life13051090</dc:identifier><dc:identifier>ISSN pri članku: 2075-1729</dc:identifier><dc:language>sl</dc:language></metadata>
