Anti-inflammatory effects of colitis-induced changes in commensal gut microbes

结肠炎引起的肠道共生微生物变化的抗炎作用

• 批准号: 8567015
• 负责人: Jonathan James Hansen
• 金额: $ 7.6万
• 依托单位: UNIV OF NORTH CAROLINA CHAPEL HILL
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-07-01 至 2015-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8567015
• 关键词: Acids; Adverse effects; Affect; American; Aminobutyric Acids; Animal Model; Anti-Inflammatory Agents; Anti-inflammatory; Antigen Presentation Pathway; Antigens; Attenuated; Bacteria; Bacterial Translocation; Bone Marrow; Chronic; Colitis; Colon; Crohn' s disease; Data; Development; Disease; Disease Progression; Enterobacteriaceae; Environment; Epithelial Cells; Epithelium; Escherichia coli; Feedback; Foundations; Future; Genes; Gnotobiotic; Goals; Heat shock proteins; Human; Immune; Immune response; Immune system; In Vitro; Infection; Inflammation; Inflammatory Bowel Diseases; Inflammatory Response; Interleukin-10; Intestinal Diseases; Intestines; Investigation; K-Series Research Career Programs; Knockout Mice; Lead; Life; Malignant Neoplasms; Mediating; Microbe; Modeling; Movement; Oxidative Stress; Pathogenesis; Pathway interactions; Persons; Phagosomes; Pharmaceutical Preparations; Process; Property; Proteins; Publishing; Research; Resistance; Role; Study Subject; System; T cell response; T-Cell Activation; Testing; Therapeutic; Tissues; Ulcerative Colitis; acid stress; antigen processing; base; biological adaptation to stress; commensal microbes; experience; human disease; innovation; killings; macrophage; microbial; microbial host; microorganism interaction; minimal risk; monolayer; novel; novel diagnostics; novel therapeutics; oxidative damage; prevent; public health relevance; therapeutic target; uptake

DESCRIPTION (provided by applicant): Human inflammatory bowel diseases (IBD's), including Crohn's disease and ulcerative colitis, are life-long, potentially debilitating intestina disorders thought to be due to overly-aggressive immune responses to normal bacteria that typically colonize the intestines. Current treatments focus on suppressing a person's immune system, which can lead to complications such as cancer and infections. The overall goal of this research is to better understand how bacteria contribute to the development of IBD's so that new medications can be developed that specifically target the intestinal microbes with minimal risk to the person. Recent data from animal models of IBD's suggest that inflammation causes intestinal bacteria to increase expression of small heat shock proteins, which in turn attenuate host inflammation. Whether anti-inflammatory properties of these heat shock proteins are also observed in other bacterial stress response systems is unknown and is the subject of these studies. Identifying and understanding the bacterial stress response systems that have anti- inflammatory properties could lead to the development of novel agents to treat IBD's by targeting master regulators of multiple bacterial stress response pathways. Preliminary data suggest that non-pathogenic E. coli in the colon also upregulate expression of acid resistance genes, gadA and gadB, during colitis and that these genes inhibit movement of the bacteria into intestinal tissues and prevent killing of E. coli by macrophages. The proposed studies aim to 1) Determine the effects of E. coli gadAB expression on the development of experimental IBD's, 2) Identify mechanisms by which E. coli gadAB expression inhibits movement of bacteria across intestinal epithelial cells, and 3) Study how E. coli GadAB promote bacterial survival within, and antigen processing by, macrophages. Interleukin-10 knockout mice, which develop spontaneous colitis when colonized by certain bacteria, will be selectively colonized with genetically altered non-pathogenic E. coli strains. In vitro studies of E. coli-infected T84 intestinal epithelial cell monolayers and bone-marrow derived macrophages will help determine mechanisms by which E. coli GadAB affects bacterial translocation and immune system activation. It is anticipated that completion of the proposed studies will: 1) identify novel functions of E. coli GadAB, 2) determine the anti-inflammatory potential of E. coli GadAB in experimental IBD's, 3) increase understanding of how IBD's develop, and 4) lead to future studies of manipulating bacterial stress responses for therapeutic purposes.

描述（由申请人提供）：人类炎症性肠病（IBD），包括克罗恩病和溃疡性结肠炎，是终身的、可能使人衰弱的肠道疾病，被认为是由于对通常定植在肠道中的正常细菌的过度攻击性免疫应答所致。目前的治疗方法集中在抑制一个人的免疫系统，这可能导致癌症和感染等并发症。这项研究的总体目标是更好地了解细菌如何促进IBD的发展，以便开发专门针对肠道微生物的新药物，对人体的风险最小。来自IBD动物模型的最新数据表明，炎症导致肠道细菌增加小热休克蛋白的表达，从而减轻宿主炎症。这些热休克蛋白的抗炎特性是否也在其他细菌应激反应系统中观察到尚不清楚，这是这些研究的主题。鉴定和理解具有抗炎特性的细菌应激反应系统可以导致通过靶向多种细菌应激反应途径的主调节剂来治疗IBD的新型药剂的开发。初步数据表明，非致病性E。结肠中的大肠杆菌也在结肠炎期间上调耐酸基因gadA和gadB的表达，并且这些基因抑制细菌进入肠组织的运动并阻止大肠杆菌的杀死。大肠埃希菌通过巨噬细胞。本研究的目的是：1）确定E. coli gadAB表达对实验性IBD发展的影响; 2）鉴定E. coligadAB的表达抑制了细菌在肠上皮细胞中的运动;大肠杆菌GadAB促进巨噬细胞内的细菌存活和抗原加工。白细胞介素-10基因敲除的小鼠，当被某些细菌定殖时会发展成自发性结肠炎，将选择性地用基因改变的非致病性E.大肠杆菌菌株。对E.大肠杆菌感染的T84肠上皮细胞 单层和骨髓来源的巨噬细胞将有助于确定E. coli GadAB影响细菌移位和免疫系统激活。预计完成拟议的研究将：1）确定新的功能，E。coli GadAB，2）测定E.大肠杆菌GadAB在实验性IBD的，3）增加了解IBD的发展，和4）导致未来的研究操纵细菌应激反应的治疗目的。