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罗伊氏乳杆菌 CRL1098 可溶性因子调节外周血单个核细胞中肿瘤坏死因子 α 的产生:脂筏的参与。

Lactobacillus reuteri CRL1098 soluble factors modulate tumor necrosis factor alpha production in peripheral blood mononuclear cells: involvement of lipid rafts.

机构信息

Centro de Referencia para Lactobacilos, CERELA-CONICET, Chacabuco 145, T4000ILC Tucumán, Argentina.

出版信息

Int Immunopharmacol. 2012 Dec;14(4):446-53. doi: 10.1016/j.intimp.2012.08.020. Epub 2012 Sep 13.

Abstract

The aim of the present study was to evaluate the capacity of Lactobacillus reuteri CRL1098 soluble factors (Lr-S) to modulate TNF-α production in peripheral blood mononuclear cells (PBMC) and to study lipid rafts participation in this response. PBMC treated with Lr-S showed a reduced production of TNF-α. In addition, Lr-S treatment activated ERK and p38 MAPK pathways in PBMC. Lipid rafts participation in the reduced production of TNF-α by PBMC induced by Lr-S was verified by lipid rafts disruption with methyl-β-cyclodextrin and the reduction of the Src-tyrosine kinase Lck localization in rafts. Moreover, PBMC pre-treatment with Lck inhibitors blocked the effect of Lr-S on TNF-α production suggesting that activation and mobilization of Lck from lipid rafts would be involved in the modulatory effect of L. reuteri CRL1098. A secreted peptide of 5785 Da would be responsible of the modulatory effect of CRL1098 strain. This study demonstrated for the first time the lipid rafts participation in a response induced by a beneficial bacterium. Also, these results open new possibilities for investigating the molecular mechanisms involved in the interaction of probiotic bacterial extracellular compounds with immune cells.

摘要

本研究旨在评估鼠李糖乳杆菌 CRL1098 可溶性因子(Lr-S)调节外周血单个核细胞(PBMC)中 TNF-α产生的能力,并研究脂筏在该反应中的参与情况。用 Lr-S 处理的 PBMC 显示 TNF-α产生减少。此外,Lr-S 处理激活了 PBMC 中的 ERK 和 p38 MAPK 途径。通过用甲基-β-环糊精破坏脂筏以及减少Src 酪氨酸激酶 Lck 在脂筏中的定位,证实了 Lr-S 诱导的 PBMC 中 TNF-α产生减少与脂筏的参与有关。此外,PBMC 用 Lck 抑制剂预处理可阻断 Lr-S 对 TNF-α产生的影响,表明 Lck 的激活和从脂筏中的动员将参与 L. reuteri CRL1098 的调节作用。分子量为 5785 Da 的分泌肽将负责 CRL1098 菌株的调节作用。本研究首次证明了脂筏参与有益细菌诱导的反应。此外,这些结果为研究益生菌细菌细胞外化合物与免疫细胞相互作用涉及的分子机制开辟了新的可能性。

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