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巨噬细胞细胞因子对共生革兰氏阳性唾液乳杆菌菌株的反应与 TLR2 无关,与 Myd88 有关。

Macrophage cytokine responses to commensal Gram-positive Lactobacillus salivarius strains are TLR2-independent and Myd88-dependent.

机构信息

APC Microbiome Ireland, University College Cork, Cork, Ireland.

School of Biochemistry and Cell Biology, University College Cork, Cork, Ireland.

出版信息

Sci Rep. 2021 Mar 15;11(1):5896. doi: 10.1038/s41598-021-85347-7.

Abstract

The mechanisms through which cells of the host innate immune system distinguish commensal bacteria from pathogens are currently unclear. Toll-like receptors (TLRs) are a class of pattern recognition receptors (PRRs) expressed by host cells which recognize microbe-associated molecular patterns (MAMPs) common to both commensal and pathogenic bacteria. Of the different TLRs, TLR2/6 recognize bacterial lipopeptides and trigger cytokines responses, especially to Gram-positive and Gram-negative pathogens. We report here that TLR2 is dispensable for triggering macrophage cytokine responses to different strains of the Gram-positive commensal bacterial species Lactobacillus salivarius. The L. salivarius UCC118 strain strongly upregulated expression of the PRRs, Mincle (Clec4e), TLR1 and TLR2 in macrophages while downregulating other TLR pathways. Cytokine responses triggered by L. salivarius UCC118 were predominantly TLR2-independent but MyD88-dependent. However, macrophage cytokine responses triggered by another Gram-positive commensal bacteria, Bifidobacterium breve UCC2003 were predominantly TLR2-dependent. Thus, we report a differential requirement for TLR2-dependency in triggering macrophage cytokine responses to different commensal Gram-positive bacteria. Furthermore, TNF-α responses to the TLR2 ligand FSL-1 and L. salivarius UCC118 were partially Mincle-dependent suggesting that PRR pathways such as Mincle contribute to the recognition of MAMPs on distinct Gram-positive commensal bacteria. Ultimately, integration of signals from these different PRR pathways and other MyD88-dependent pathways may determine immune responses to commensal bacteria at the host-microbe interface.

摘要

目前尚不清楚宿主固有免疫系统的细胞如何区分共生菌和病原体。Toll 样受体(TLR)是宿主细胞表达的一类模式识别受体(PRR),可识别共生菌和病原菌共有的微生物相关分子模式(MAMP)。在不同的 TLR 中,TLR2/6 识别细菌脂肽并触发细胞因子反应,特别是针对革兰氏阳性和革兰氏阴性病原体。我们在这里报告,TLR2 对于触发巨噬细胞对不同株革兰氏阳性共生细菌乳杆菌的细胞因子反应是可有可无的。乳杆菌 UCC118 株强烈地上调了巨噬细胞中 PRR(Mincle(Clec4e))、TLR1 和 TLR2 的表达,同时下调了其他 TLR 途径。乳杆菌 UCC118 触发的细胞因子反应主要是非 TLR2 依赖性但 MyD88 依赖性的。然而,另一种革兰氏阳性共生菌短双歧杆菌 UCC2003 触发的巨噬细胞细胞因子反应主要依赖于 TLR2。因此,我们报告了触发不同革兰氏阳性共生菌的巨噬细胞细胞因子反应对 TLR2 依赖性的差异需求。此外,TLR2 配体 FSL-1 和乳杆菌 UCC118 对 TNF-α的反应部分依赖于 Mincle,表明 PRR 途径(如 Mincle)有助于识别不同革兰氏阳性共生菌的 MAMP。最终,这些不同的 PRR 途径和其他 MyD88 依赖性途径的信号整合可能决定了宿主-微生物界面共生菌的免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad36/7961041/89aa793a6bae/41598_2021_85347_Fig1_HTML.jpg

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