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Formyl peptide receptors as mediators of intestinal mucosal homeostasis

甲酰基肽受体作为肠粘膜稳态调节剂

基本信息

批准号：
8667429
负责人：
ASMA NUSRAT
金额：
$ 40.01万
依托单位：
EMORY UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2011
资助国家：
美国
起止时间：
2011-09-01 至 2016-05-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8667429
关键词：
Actins Acute Agonist Annexins Anti-Inflammatory Agents Anti-inflammatory Apoptosis Bacteria Biochemical Biological Biological Process Chemicals Clinical Complex Coupled Development Disease Drug or chemical Tissue Distribution Enteral Environment Epithelial Epithelial Cell Proliferation Epithelial Cells Epithelium Epitopes Event FPR1 gene Family member Focal Adhesion Kinase 1 GTP-Binding Proteins Generations Growth Guanine Nucleotide Exchange Factors Guanosine Triphosphate Phosphohydrolases Homeostasis Imaging Techniques Infection Inflammation Inflammation Mediators Inflammatory Inflammatory Bowel Diseases Injury Intestinal Mucosa Intestines Ischemia Knockout Mice Laboratories Ligands Lipids MAP Kinase Gene Maintenance Mechanics Mediating Mediator of activation protein Microbe Modification Molecular Monoclonal Antibodies Mucositis NADPH Oxidase Natural regeneration Operative Surgical Procedures Outcome Oxidation-Reduction Pathogenesis Pathologic Pathway interactions Patients Pattern recognition receptor Peptides Phagocytes Physiological Processes Play Post-Translational Protein Processing Process Production Proliferating Property Protein Tyrosine Phosphatase Proteins Proteomics Reactive Oxygen Species Receptor Activation Receptor Signaling Recovery Regulation Resolution Role Signal Pathway Signal Transduction Site-Directed Mutagenesis Spatial Distribution Surface Therapeutic Therapeutic Agents Tissues cell motility fMet-Leu-Phe receptor formyl peptide gastrointestinal epithelium in vivo intestinal epithelium intestinal homeostasis lipoxin A4 migration molecular imaging mouse model novel protein complex receptor response to injury small molecule wound

项目摘要

DESCRIPTION (provided by applicant): The gastrointestinal epithelium functions as a dynamic barrier that serves as an interface between luminal contents and underlying tissue compartments, and is thus vital in maintaining mucosal homeostasis. Mucosal wounds have been observed following enteric infection, inflammatory bowel disease and ischemic insults. Disruption of the critical epithelial barrier allows access of luminal contents to immunologically privileged compartments thereby contributing to disease pathogenesis. In response to injury, intestinal epithelial cells (IEC) migrate and proliferate to rapidly cover denuded surfaces and re-establish the epithelia barrier. We have recently identified expression of the N-formyl peptide receptors (FPR1 and FPR2) in the intestinal epithelium. Our studies determined that a bacterial derived N-formyl peptide, fMLF and the endogenous Annexin 1 protein, which are agonists for FPR family members, promote intestinal epithelial cell migration and facilitate wound closure. Additionally, it is becoming evident that a healthy optimized intestinal microflora mediates important roles in normal gut homeostasis and recovery from mucosal insults. Recent experimental results in our laboratory revealed that epithelial cells exposed to fMLF and intact bacteria also rapidly initiate cytoplasmic signaling events, Rac and Cdc2 activation, reactive oxygen species (ROS) production, epithelial cell migration and wound closure. Thus, we believe that FPRs represent important novel type of pattern recognition receptors (PRR) in the intestinal epithelium that transmit homeostatic signaling and facilitate epithelial barrier recovery following pathologic insults. Thus, our overall objectives are to define the pathobiologic function of epithelial FPRs and microbiota in regulating intestinal homeostasis, barrier recovery and resolution of inflammation.

描述（由申请人提供）：胃肠道上皮作为一种动态屏障，作为管腔内容物和底层组织隔室之间的界面，因此对维持粘膜稳态至关重要。在肠道感染、炎症性肠病和缺血性损伤后，也观察到粘膜损伤。关键上皮屏障的破坏允许管腔内容物进入免疫特权室，从而促进疾病的发病机制。作为对损伤的反应，肠上皮细胞（IEC）迁移和增殖以迅速覆盖脱落表面并重建上皮屏障。我们最近发现了肠上皮中n -甲酰基肽受体（FPR1和FPR2）的表达。我们的研究发现，细菌衍生的n -甲酰基肽、fMLF和内源性膜联蛋白1是FPR家族成员的激动剂，可促进肠上皮细胞迁移并促进伤口愈合。此外，越来越明显的是，健康优化的肠道菌群在正常肠道稳态和粘膜损伤恢复中起着重要作用。我们实验室最近的实验结果表明，暴露于fMLF和完整细菌的上皮细胞也能迅速启动细胞质信号事件，激活Rac和Cdc2，产生活性氧（ROS），上皮细胞迁移和伤口愈合。因此，我们认为fpr代表了肠上皮中重要的新型模式识别受体（PRR），其传递稳态信号并促进病理性损伤后上皮屏障的恢复。因此，我们的总体目标是确定上皮fpr和微生物群在调节肠道稳态、屏障恢复和炎症消退中的病理生物学功能。