4 research outputs found
ノウコウソク カンジャ ヘ ノ サイハツ ヨボウ シドウ ニ タイスル カンゴシ ノ ニンシキ ト ジッシ ジョウキョウ ノ ヘンヨウ - ノウコウソク サイハツ ヨボウ シドウ ニ カンスル ベンキョウカイ オ トオシテ -
Cloning, functional expression and tissue distribution of rabbit α1d-adrenoceptor1The nucleotide sequence reported in this paper has been submitted to the GenBank under the accession number U64032.1
Commensal Lactobacillus Controls Immune Tolerance during Acute Liver Injury in Mice
Summary: Gut-derived microbial antigens trigger the innate immune system during acute liver injury. During recovery, regulatory immunity plays a role in suppressing inflammation; however, the precise mechanism underlying this process remains obscure. Here, we find that recruitment of immune-regulatory classical dendritic cells (cDCs) is crucial for liver tolerance in concanavalin A-induced acute liver injury. Acute liver injury resulted in enrichment of commensal Lactobacillus in the gut. Notably, Lactobacillus activated IL-22 production by gut innate lymphoid cells and raised systemic IL-22 levels. Gut-derived IL-22 enhanced mucosal barrier function and promoted the recruitment of regulatory cDCs to the liver. These cDCs produced IL-10 and TGF-β through TLR9 activation, preventing further liver inflammation. Collectively, our results indicate that beneficial gut microbes influence tolerogenic immune responses in the liver. Therefore, modulation of the gut microbiota might be a potential option to regulate liver tolerance. : Nakamoto et.al. find that Lactobacillus accumulates in the gut and activates IL-22 production by innate lymphoid cells during acute liver injury. Gut-derived IL-22 contributes to liver tolerance via induction of regulatory DCs. Keywords: immune tolerance, dendritic cell, innate lymphoid cell, acute liver injury, interleukin-10, interleukin-22, microbiota, dysbiosi