Distinctive probiotic features share common TLR2-dependent signalling in intestinal epithelial cells.
Distinctive probiotic features share common TLR2-dependent signalling in intestinal epithelial cells.
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DOI:
10.1111/cmi.13264
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发表时间:
2021-01
影响因子:
3.4
通讯作者:
Rogelj I
中科院分区:
文献类型:
--
作者:
Paveljšek D;Ivičak-Kocjan K;Treven P;Benčina M;Jerala R;Rogelj I
The underlying mechanisms of probiotics and postbiotics are not well understood, but it is known that both affect the adaptive and innate immune responses. In addition, there is a growing concept that some probiotic strains have common core mechanisms that provide certain health benefits. Here, we aimed to elucidate the signalization of the probiotic bacterial strains Lactobacillus paragasseri K7, Limosilactobacillus fermentum L930BB, Bifidobacterium animalis subsp. animalis IM386 and Lactiplantibacillus plantarum WCFS1. We showed in in vitro experiments that the tested probiotics exhibit common TLR2‐ and TLR10‐dependent downstream signalling cascades involving inhibition of NF‐κB signal transduction. Under inflammatory conditions, the probiotics activated phosphatidylinositol 3‐kinase (PI3K)/Akt anti‐apoptotic pathways and protein kinase C (PKC)‐dependent pathways, which led to regulation of the actin cytoskeleton and tight junctions. These pathways contribute to the regeneration of the intestinal epithelium and modulation of the mucosal immune system, which, together with the inhibition of canonical TLR signalling, promote general immune tolerance. With this study we identified shared probiotic mechanisms and were the first to pinpoint the role of anti‐inflammatory probiotic signalling through TLR10.
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DOI:
10.4049/jimmunol.1502599
发表时间:
2016-05-01
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Jiang S;Li X;Hess NJ;Guan Y;Tapping RI
通讯作者:
Tapping RI
影响因子:
1.2
作者:
Baeuerl, Christine;Perez-Martinez, Gaspar;Monedero, Vicente
通讯作者:
Monedero, Vicente
影响因子:
13.6
作者:
Jiménez-Dalmaroni MJ;Gerswhin ME;Adamopoulos IE
通讯作者:
Adamopoulos IE
影响因子:
32.4
作者:
Price AE;Shamardani K;Lugo KA;Deguine J;Roberts AW;Lee BL;Barton GM
通讯作者:
Barton GM
影响因子:
4.3
作者:
Shen ZH;Zhu CX;Quan YS;Yang ZY;Wu S;Luo WW;Tan B;Wang XY
通讯作者:
Wang XY