课题基金 / 基金详情

项目摘要

项目成果

James Versalovic的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): The central goal of this proposal is to understand molecular mechanisms of probiosis for new treatment and prevention strategies in inflammatory bowel disease. This proposal includes comprehensive genetic and peptidomic approaches in order to determine the molecular basis of anti-inflammatory functions by probiotics. Our laboratory has obtained evidence for novel mechanisms of probiosis including inhibition of pro-inflammatory TNFa production by macrophages. Intestinal lactobacilli have been isolated and tested for tumor necrosis factor-alpha (TNF-a)-inhibitory activity. The overall hypothesis is that probiotic intestinal Lactobacillus strains secrete peptides that suppress TNF-a signaling in macrophages and inhibit intestinal inflammation. The functions of candidate Lactobacillus genes that regulate probiotic activities including peptide secretion will be studied in vitro using macrophages activated by Toll-like receptor agonists. Wild type lactobacilli and knockout Lactobacillus strains lacking anti-inflammatory effects in vitro will be administered to IL-10-deficient mice in order to explore mechanisms of probiotic action in vivo. Identification of probiotic genes encoding anti-inflammatory functions and probiotic response pathways in macrophages may provide valuable insights into potential human targets for probiotic action in Crohn's disease. 1. Specify probiotic anti-inflammatory genes in intestinal Lactobacillus strains by knockout mutagenesis. 2. Identify anti-inflammatory glutamate-containing peptides by comparative peptidomics of the Lactobacillus secretome. 3. Compare mucosal inflammatory responses in the intestines of IL-10-deficient mice colonized with knockout or wild type isogenic strains of probiotic Lactobacillus. These studies will facilitate the identification of beneficial bacteria that can be used to treat inflammatory bowel disease such as Crohn's disease and ulcerative colitis. We seek to understand the mechanisms of action of beneficial intestinal bacteria so that new strains can be identified naturally or engineered for human medicine.
期刊论文(16)
专著(0)
科研奖励(0)
会议论文
Histamine derived from probiotic Lactobacillus reuteri suppresses TNF via modulation of PKA and ERK signaling.
源自益生菌乳酸杆菌的组胺通过调节PKA和ERK信号传导抑制TNF。
DOI: 10.1371/journal.pone.0031951
发表时间: 2012
期刊: PloS one
影响因子: 3.7
作者: [Thomas CM, Hong T, van Pijkeren JP, Hemarajata P, Trinh DV, Hu W, Britton RA, Kalkum M, Versalovic J]
通讯作者: Versalovic J
Lactobacillus saerimneri and Lactobacillus ruminis: novel human-derived probiotic strains with immunomodulatory activities.
Saerimneri和Ruminis乳酸乳杆菌:具有免疫调节活性的新型人类源自益生菌菌株。
DOI: 10.1111/j.1574-6968.2009.01506.x
发表时间: 2009-04
期刊: FEMS microbiology letters
影响因子: 2.1
作者: [Taweechotipatr M, Iyer C, Spinler JK, Versalovic J, Tumwasorn S]
通讯作者: Tumwasorn S
DOI: 10.1016/j.cppeds.2008.09.001
发表时间: 2008-11-01
期刊: Current problems in pediatric and adolescent health care
影响因子: 1.6
作者: [Hsieh, Michael H, Versalovic, James]
通讯作者: Versalovic, James
DOI: 10.1373/clinchem.2012.187617
发表时间: 2013-04
期刊: Clinical chemistry
影响因子: 9.3
作者: [Devaraj S, Hemarajata P, Versalovic J]
通讯作者: Versalovic J
9
    Gut L-Histidine Metabolism and Histamine Signaling in Colonic Neoplasia
    • 批准号:
      8581697
    • 项目类别:
    • 资助金额:
      $60.22万
    • 财政年份:
      2013
    • 负责人:
      James Versalovic
    • 依托单位:
    Gut L-Histidine Metabolism and Histamine Signaling in Colonic Neoplasia
    • 批准号:
      8711382
    • 项目类别:
    • 资助金额:
      $59.71万
    • 财政年份:
      2013
    • 负责人:
      James Versalovic
    • 依托单位:
    Gut L-Histidine Metabolism and Histamine Signaling in Colonic Neoplasia
    • 批准号:
      9324137
    • 项目类别:
    • 资助金额:
      $45.21万
    • 财政年份:
      2013
    • 负责人:
      James Versalovic
    • 依托单位:
    INFLUENCE OF DIET ON DEVELOPMENT OF INTESTINAL MICROBIOTA
    • 批准号:
      8356741
    • 项目类别:
    • 资助金额:
      $2.05万
    • 财政年份:
      2010
    • 负责人:
      James Versalovic
    • 依托单位:
    海外基金