Investigating immumomodulatory mechanisms of probiotics

研究益生菌的免疫调节机制

基本信息

  • 批准号:
    312482-2013
  • 负责人:
  • 金额:
    $ 3.13万
  • 依托单位:
  • 依托单位国家:
    加拿大
  • 项目类别:
    Discovery Grants Program - Individual
  • 财政年份:
    2015
  • 资助国家:
    加拿大
  • 起止时间:
    2015-01-01 至 2016-12-31
  • 项目状态:
    已结题

项目摘要

Commensal microbes live inside the host in symbiosis. Probiotics are live commensals that have been used for centuries to replenish normal or beneficial gut and urogenital microflora. Long-term objectives of my research program are to understand how the host maintains immunological symbiosis with commensals and what immunological effects probiotics have on the host. During the last 5 years of NSERC support, our research program has focused on unraveling the mechanisms of the host cells in sensing bacterial probiotics and their effects on the host immune responses. We have demonstrated that the probiotic strain of Lactobacillus rhamnosus GR1 (GR1) and its secreted products have immunomodulatory effects on macrophages, dendritic cells, intestinal lamina propria cells and placental trophoblasts. GR1 as well as other strains of Lactobacillus rhamnosus preferentially and potently produce the immunomodulatory cytokine granulocyte colony-stimulating factor (G-CSF) in these cells, which may play important roles in maintaining immunological homeostasis of intestine and placenta. This research proposal is to further study the cellular and signaling mechanisms by which GR1, GR1-secreted factor(s) and G-CSF in modulating macrophage differentiation, activation and survival. The followings are specific aims of the study: Aim 1: Identify/purify the GR1-factor(s), and examine its/their signaling and epigenetic mechanisms responsible for preferential production of G-CSF in macrophages. Aim 2. Examining the role and mechanisms of G-CSF in macrophage differentiation and survival in bone marrow cells, THP-1 cells and the intestine. The proposed study will provide detailed information on how lactobacilli modulate macrophage activation and how G-CSF highly produced by lactobacillus-exposed macrophages affects myeloid cell differentiation and cell survival. Overall, these studies will unravel how commensals and probiotics modulate the host immune system and maintain symbiosis in the host.
共生微生物在宿主体内共生。益生菌是活的共生菌,几个世纪以来一直被用来补充正常或有益的肠道和泌尿生殖菌群。我的研究计划的长期目标是了解宿主如何与共生体维持免疫共生以及益生菌对宿主的免疫影响。在 NSERC 的过去 5 年支持中,我们的研究项目致力于揭示宿主细胞感知细菌益生菌的机制及其对宿主免疫反应的影响。我们已经证明,益生菌鼠李糖乳杆菌GR1(GR1)及其分泌产物对巨噬细胞、树突状细胞、肠固有层细胞和胎盘滋养层细胞具有免疫调节作用。 GR1以及其他鼠李糖乳杆菌菌株在这些细胞中优先有效地产生免疫调节细胞因子粒细胞集落刺激因子(G-CSF),这可能在维持肠道和胎盘的免疫稳态中发挥重要作用。本研究计划旨在进一步研究 GR1、GR1 分泌因子和 G-CSF 调节巨噬细胞分化、激活和存活的细胞和信号传导机制。该研究的具体目标如下: 目标 1:鉴定/纯化 GR1 因子,并检查其负责巨噬细胞中优先产生 G-CSF 的信号传导和表观遗传机制。 目标 2. 检查 G-CSF 在骨髓细胞、THP-1 细胞和肠道中巨噬细胞分化和存活中的作用和机制。 拟议的研究将提供有关乳杆菌如何调节巨噬细胞活化以及乳杆菌暴露的巨噬细胞大量产生的 G-CSF 如何影响骨髓细胞分化和细胞存活的详细信息。总的来说,这些研究将揭示共生菌和益生菌如何调节宿主免疫系统并维持宿主共生。

项目成果

期刊论文数量(0)
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科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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Kim, SungOuk其他文献

Kim, SungOuk的其他文献

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{{ truncateString('Kim, SungOuk', 18)}}的其他基金

HISTONE DEACETYLASES IN EPIGENETIC MODULATION OF MACROPHAGE ACTIVATION AND TRAINING
组蛋白脱乙酰酶在巨噬细胞激活和训练的表观遗传调节中的作用
  • 批准号:
    RGPIN-2018-05514
  • 财政年份:
    2020
  • 资助金额:
    $ 3.13万
  • 项目类别:
    Discovery Grants Program - Individual
HISTONE DEACETYLASES IN EPIGENETIC MODULATION OF MACROPHAGE ACTIVATION AND TRAINING
组蛋白脱乙酰酶在巨噬细胞激活和训练的表观遗传调节中的作用
  • 批准号:
    RGPIN-2018-05514
  • 财政年份:
    2019
  • 资助金额:
    $ 3.13万
  • 项目类别:
    Discovery Grants Program - Individual
HISTONE DEACETYLASES IN EPIGENETIC MODULATION OF MACROPHAGE ACTIVATION AND TRAINING
组蛋白脱乙酰酶在巨噬细胞激活和训练的表观遗传调节中的作用
  • 批准号:
    RGPIN-2018-05514
  • 财政年份:
    2018
  • 资助金额:
    $ 3.13万
  • 项目类别:
    Discovery Grants Program - Individual
Investigating immumomodulatory mechanisms of probiotics
研究益生菌的免疫调节机制
  • 批准号:
    312482-2013
  • 财政年份:
    2017
  • 资助金额:
    $ 3.13万
  • 项目类别:
    Discovery Grants Program - Individual
Investigating immumomodulatory mechanisms of probiotics
研究益生菌的免疫调节机制
  • 批准号:
    312482-2013
  • 财政年份:
    2016
  • 资助金额:
    $ 3.13万
  • 项目类别:
    Discovery Grants Program - Individual
Investigating immumomodulatory mechanisms of probiotics
研究益生菌的免疫调节机制
  • 批准号:
    312482-2013
  • 财政年份:
    2014
  • 资助金额:
    $ 3.13万
  • 项目类别:
    Discovery Grants Program - Individual
Investigating immumomodulatory mechanisms of probiotics
研究益生菌的免疫调节机制
  • 批准号:
    312482-2013
  • 财政年份:
    2013
  • 资助金额:
    $ 3.13万
  • 项目类别:
    Discovery Grants Program - Individual
Investigating immunomodulating mechanisms of probiotics
研究益生菌的免疫调节机制
  • 批准号:
    312482-2008
  • 财政年份:
    2012
  • 资助金额:
    $ 3.13万
  • 项目类别:
    Discovery Grants Program - Individual
Investigating immunomodulating mechanisms of probiotics
研究益生菌的免疫调节机制
  • 批准号:
    312482-2008
  • 财政年份:
    2011
  • 资助金额:
    $ 3.13万
  • 项目类别:
    Discovery Grants Program - Individual
Investigating immunomodulating mechanisms of probiotics
研究益生菌的免疫调节机制
  • 批准号:
    312482-2008
  • 财政年份:
    2010
  • 资助金额:
    $ 3.13万
  • 项目类别:
    Discovery Grants Program - Individual

相似海外基金

Investigating immumomodulatory mechanisms of probiotics
研究益生菌的免疫调节机制
  • 批准号:
    312482-2013
  • 财政年份:
    2017
  • 资助金额:
    $ 3.13万
  • 项目类别:
    Discovery Grants Program - Individual
Investigating immumomodulatory mechanisms of probiotics
研究益生菌的免疫调节机制
  • 批准号:
    312482-2013
  • 财政年份:
    2016
  • 资助金额:
    $ 3.13万
  • 项目类别:
    Discovery Grants Program - Individual
Investigating immumomodulatory mechanisms of probiotics
研究益生菌的免疫调节机制
  • 批准号:
    312482-2013
  • 财政年份:
    2014
  • 资助金额:
    $ 3.13万
  • 项目类别:
    Discovery Grants Program - Individual
Investigating immumomodulatory mechanisms of probiotics
研究益生菌的免疫调节机制
  • 批准号:
    312482-2013
  • 财政年份:
    2013
  • 资助金额:
    $ 3.13万
  • 项目类别:
    Discovery Grants Program - Individual
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