食品科学

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嗜酸乳酸杆菌对自主活动受限型应激小鼠肠道黏膜免疫状态的影响

郝凤奇1,李景梅1,*,杨桂连2,*   

  1. 1.长春理工大学生命科学技术学院,吉林 长春 130022;2.吉林农业大学动物科学技术学院,吉林 长春 130118
  • 出版日期:2015-12-15 发布日期:2015-12-24

Influence of Lactobacillus acidophilus on Intestinal Mucosal Immunity in a Mouse Model of Stress Induced by Auto-Activity Restriction

HAO Fengqi1, LI Jingmei1,*, YANG Guilian2,*   

  1. 1. School of Life Science and Technology, Changchun University of Science and Technology, Changchun 130022, China;
    2. College of Animal Science and Technology, Jilin Agricultural University, Changchun 130118, China
  • Online:2015-12-15 Published:2015-12-24

摘要:

目的:探讨嗜酸乳酸杆菌(Lactobacillus acidophilus,LA)对自主活动受限型应激小鼠肠道黏膜免疫状态的影响。方法:以健康雌性BALB/c小鼠为受试动物,分为常规饲养组(NC组)、常规饲养条件灌胃LA组(NC+LA组)、应激组(S组)、应激条件灌胃LA组(S+LA组),小鼠的LA灌胃剂量为108 CFU/d;应激组小鼠每天被限制自主活动3 h;15 d后取材,采用流式细胞术、酶联免疫吸附(enzyme-linked immunosorbent assay,ELISA)等方法,对肠系膜淋巴结(mesenteric lymph nodes,MLN)中CD4+T细胞、CD8+T细胞和CD11c+树突细胞(CD11c+ dendritic cell,CD11c+ DC)比例,结肠组织白细胞介素-10(interleukin-10,IL-10)和白细胞介素-17(interleukin-17,IL-17)水平,以及小肠总分泌型免疫球蛋白A(secreted immunoglobulin A,sIgA)水平进行检测。结果:常规饲养条件下,LA能极显著提高小鼠MLN中CD4+T细胞比例(P<0.01),显著提高MLN中CD11c+ DC比例、小肠总sIgA水平和结肠组织IL-10水平(P<0.05),显著降低结肠组织IL-17水平(P<0.05),而对MLN中CD8+T细胞比例无显著影响(P>0.05);应激条件能极显著降低小鼠MLN中CD4+T细胞比例和CD11c+ DC比例(P<0.01),显著降低CD8+T细胞比例(P<0.05),极显著降低小鼠结肠组织IL-10水平和小肠总sIgA水平(P<0.01),极显著提高结肠组织IL-17水平(P<0.01);应激条件下,LA能显著提高小鼠MLN中CD4+T细胞比例和CD11c+ DC比例(P<0.05),显著提高小鼠结肠组织IL-10水平和小肠总sIgA水平(P<0.05),并显著降低结肠组织IL-17水平(P<0.05),而对小鼠MLN中CD8+T细胞比例无显著影响(P>0.05)。结论:给予自主活动受限型应激小鼠LA干预,可提高小鼠MLN中CD4+T细胞和CD11c+ DC比例,上调结肠IL-10和小肠总sIgA分泌水平,下调结肠IL-17分泌水平,调节应激小鼠的肠道黏膜免疫状态。

关键词: 嗜酸乳酸杆菌, 自主活动受限, 应激, 肠道黏膜免疫

Abstract:

Objective: To assess the influence of Lactobacillus acidophilus on intestinal mucosal immunity in a mouse
model of stress induced by auto-activity restriction. Methods: Male health BALB/c mice were divided into 4 groups. In
normal control group (NC), the mice received balanced diet and water and were left undisturbed in their cages. In NC
plus Lactobacillus acidophilus (NC + LA) group, the mice were given a suspension of LA with 108 CFU/d per mouse
through intragastric administration under normal control condition. In stress group (S), the mice were subjected to stress
induced by auto-activity restriction for 3 h per day. In stress plus LA (S+LA) group, the mice were given a suspension of
LA with 108 CFU/d per mouse through intragastric administration under stress condition. After 15 days, mice from each
group were sacrificed. CD4+T, CD8+T and CD11c+ dendritic cells (CD11c+ DCs) in mesenteric lymph nodes (MLN),
interleukin-10 (IL-10) and interleukin-17 (IL-17) levels in colon tissue, total secretory immunoglobulin A (sIgA) level in
small intestine were analyzed by flow cytometry and enzyme-linked immunosorbent assay (ELISA). Results: Under NC
condition, the proportions of CD4+T cells and CD11c+ DCs in MLN (CD4+T cell: P < 0.01, CD11c+ DC: P < 0.05), small
intestinal sIgA level and IL-10 level in colon tissue (sIgA, IL-10: P < 0.05) were enhanced by LA and IL-17 level in colon
tissue was decreased (P < 0.05), but the proportion of CD8+T cells in MLN was not significantly varied (P > 0.05). After
auto-activity restriction, the proportions of CD4+T cells, CD8+T cells and CD11c+ DCs, and the levels of IL-10 and small
intestinal sIgA were decreased (CD4+T cell, CD11c+ DC, IL-10, sIgA: P < 0.01, CD8+T cell: P < 0.05). Interestingly, the
proportion of CD4+T cells and CD11c+ DCs, the levels of IL-10 and small intestinal sIgA were increased, and the level of
IL-17 was decreased by LA under stress condition (P < 0.05), but the proportion of CD8+T cells was not significantly affected
(P > 0.05). Conclusion: LA administered to mice subjected to auto-activity restriction enhances the proportions of
CD4+T cells and CD11c+ DCs in MLN, up-regulates the levels of IL-10 in colon and total small intestinal sIgA, and downregulates
the level of IL-17 in colon, thereby modulating their intestinal mucosal immunity under stress condition.

Key words: Lactobacillus acidophilus, auto-activity restriction, stress, intestinal mucosal immunity

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