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口服嗜酸乳杆菌可通过诱导耐受性树突状细胞减轻小鼠动脉粥样硬化。

Oral administration of the lactic acid bacterium Pediococcus acidilactici attenuates atherosclerosis in mice by inducing tolerogenic dendritic cells.

作者信息

Mizoguchi Taiji, Kasahara Kazuyuki, Yamashita Tomoya, Sasaki Naoto, Yodoi Keiko, Matsumoto Takuya, Emoto Takuo, Hayashi Tomohiro, Kitano Naoki, Yoshida Naofumi, Amin Hilman Zulkifli, Hirata Ken-Ichi

机构信息

Division of Cardiovascular Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, 7-5-1, Kusunoki-cho, Chuo-ku, Kobe, 650-0017, Japan.

出版信息

Heart Vessels. 2017 Jun;32(6):768-776. doi: 10.1007/s00380-017-0949-8. Epub 2017 Feb 8.

DOI:10.1007/s00380-017-0949-8
PMID:28181012
Abstract

The intestinal microbiota appears to play an important role in the development of atherosclerosis. We investigated the effect of the probiotic lactic acid bacterium Pediococcus acidilactici R037 on atherosclerosis using apolipoprotein E-deficient (ApoE ) mice. Six-week-old ApoE mice were orally administered R037 six times a week. Mice treated with R037 for 12 weeks exhibited markedly attenuated atherosclerotic lesions in the aortic root (2.3 ± 0.15 × 10 µm vs. 3.3 ± 0.29 × 10 µm, respectively; P < 0.01; n = 15-17 each group). The expression of Ki-67 in CD4 T cells, the population of interferon γ-producing CD4 T cells in the spleen, and pro-inflammatory cytokine production from splenic lymphocytes were significantly decreased in R037-treated mice. Interestingly, splenic dendritic cells (DCs) isolated from R037-treated mice suppressed CD4 T-cell proliferation and pro-inflammatory cytokine production ex vivo, suggesting that R037 treatment induced tolerogenic DCs. Programmed cell death ligand 1 expression in DCs was significantly enhanced in R037-treated mice, which might explain the immunosuppressive effect of DCs at least in part. These results indicate that R037 attenuates atherosclerosis by inducing tolerogenic DCs, which suppress Th1-driven inflammation and the proliferative activity of CD4 T cells. Our findings may provide a novel therapeutic approach for the prevention of atherosclerosis based on dietary supplementation with probiotics.

摘要

肠道微生物群似乎在动脉粥样硬化的发展中起重要作用。我们使用载脂蛋白E缺陷(ApoE)小鼠研究了益生菌嗜酸乳杆菌罗伊氏乳杆菌R037对动脉粥样硬化的影响。六周龄的ApoE小鼠每周口服R037六次。用R037治疗12周的小鼠主动脉根部的动脉粥样硬化病变明显减轻(分别为2.3±0.15×10⁶μm和3.3±0.29×10⁶μm;P<0.01;每组n = 15 - 17)。在R037治疗的小鼠中,CD4 T细胞中Ki-67的表达、脾脏中产生干扰素γ的CD4 T细胞群体以及脾淋巴细胞产生的促炎细胞因子均显著降低。有趣的是,从R037治疗的小鼠中分离出的脾树突状细胞(DCs)在体外抑制CD4 T细胞增殖和促炎细胞因子产生,表明R037治疗诱导了耐受性DCs。在R037治疗的小鼠中,DCs中程序性细胞死亡配体1的表达显著增强,这可能至少部分解释了DCs的免疫抑制作用。这些结果表明,R037通过诱导耐受性DCs减轻动脉粥样硬化,耐受性DCs抑制Th1驱动的炎症和CD4 T细胞的增殖活性。我们的研究结果可能为基于益生菌膳食补充预防动脉粥样硬化提供一种新的治疗方法。

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