New approaches to study Pseudomonas-host interactions

研究假单胞菌与宿主相互作用的新方法

• 批准号: 8468617
• 负责人: Joanne N. Engel
• 金额: $ 32.35万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2005
• 资助国家: 美国
• 起止时间: 2005-05-01 至 2015-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8468617
• 关键词: ADP Ribose Transferases; Abbreviations; Adherens Junction; Adhesions; Anti-Bacterial Agents; Apical; Bacteria; Binding; Biology; Cancer Biology; Canis familiaris; Cell Polarity; Cells; Cellular Structures; Characteristics; Chemicals; Chinese Hamster; Collaborations; Collection; Complex; Confocal Microscopy; Cystic Fibrosis; Cytochalasin D; Cytoplasm; Data; Defect; Development; Developmental Biology; Disease; Dominant-Negative Mutation; Double-Stranded RNA; Drug Targeting; E-Cadherin; EGF gene; Epidermal Growth Factor; Epidermal Growth Factor Receptor; Epithelial; Epithelial Cells; Epithelium; Event; Feedback; Flagella; GTPase-Activating Proteins; Goals; Grant; Growth Factor; Growth Factor Receptors; Helicobacter pylori; Heparan Sulfate Proteoglycan; Human; Image; Immune system; Immunocompromised Host; Immunofluorescence Immunologic; Infection; Injury; Integration Host Factors; Kidney; Kinetics; Lead; Lipids; Maintenance; Mediator of activation protein; Membrane; Microscopy; Morbidity - disease rate; Morphology; Neisseria meningitidis; Ovary; PH Domain; Pathogenesis; Phosphatidylinositols; Phosphotransferases; Pilum; Platelet-Derived Growth Factor; Process; Production; Protein Kinase; Proteins; Proto-Oncogene Proteins c-akt; Pseudomonas; Pseudomonas aeruginosa; RNA Interference; RNA-Induced Silencing Complex; Receptor Cell; Recruitment Activity; Regulation; Resistance; Series; Signal Transduction; Small Interfering RNA; Surface; System; Testing; Therapeutic; Tight Junctions; Time; Transferase; Transgenes; Type III Secretion System Pathway; Virulent; Wound Healing; antimicrobial; apical membrane; base; basolateral membrane; cell type; enteropathogenic Escherichia coli; human disease; inhibitor/antagonist; inorganic phosphate; latrunculin A; man; microbial; microorganism; monolayer; mortality; mutant; nectin; novel; novel strategies; novel therapeutic intervention; pathogen; phosphoinositide-3,4,5-triphosphate; phosphoinositide-3,4-bisphosphate; prevent; protein E; public health relevance; red fluorescent protein; time use; trafficking; trans-Golgi Network

DESCRIPTION (provided by applicant): The ability of a pathogen to breach the highly polarized host mucosal epithelial barrier is an early and critical step in the pathogenesis of microbial infections. This event is particularly crucial for opportunistic pathogens such as Pseudomonas aeruginosa (PA), one of the most virulent opportunistic pathogens of man. Our long-term goals are to understand how pathogens in general, and PA in particular, overcome the host epithelial barrier to cause human disease. PA binds to the apical (AP) surface of polarized epithelial cells and triggers fundamental changes in the host cell that allow bacterial internalization. During this granting period, we have discovered that PA induces a remarkable local change in the morphology of the AP surface to form a membranous protrusion composed of basolateral (BL) constituents. This protrusion is the likely conduit for bacterial entry. This profound shift in the local identity of the AP membrane is the first known morphologic landmark of the effect of PA on epithelial cell monolayers. Based on our data, we hypothesize that PA can exploit small defects in epithelial polarity at the mucosal barrier to initiative a series of events that result in a positive feedback loop induces a remarkable morphologic change in which AP membrane is transformed into BL membrane. A protrusion, with characteristics of a nascent AJ, is formed that functions as a conduit for bacterial entry. By manipulating epithelial cell polarity, PA is able to enhance its bacterial binding and entry, possibly by increasing the presentation of host cell receptors or other factors that promote internalization. Our aims are to (1) Determine which key regulatory and structural components of TJ and AJ are recruited to the protrusion. (2) Determine the temporal and functional relationship between protrusion formation and bacterial entry. (3) Perform mechanistic studies to uncover how PA hijacks host cell vesicular trafficking to redirect these junctional and BL components to the AP surface. (4) Identify the bacterial determinants of protrusion formation. Together, these studies will comprehensively dissect the interactions between PA and host cell epithelium. They will identify host factors that the bacteria exploit to cause disease. The use of pathogens to study fundamental processes in mammalian biology, such as the establishment and the maintenance of epithelial polarity, has broad ramifications for many fields in addition to pathogenesis, including cancer and developmental biology. Furthermore, these host cell factors may serve as novel targets for the development of anti-bacterial therapeutics; because the drug targets host but not bacterial molecules, they are much less likely to engender resistance compared to conventional anti- microbial therapies.

描述（由申请方提供）：病原体破坏高度极化的宿主粘膜上皮屏障的能力是微生物感染发病机制的早期关键步骤。这一事件是特别重要的机会致病菌，如铜绿假单胞菌（PA），最致命的机会致病菌之一的man. Our长期目标是了解病原体一般，PA特别是如何克服宿主上皮屏障，导致人类疾病。PA与极化上皮细胞的顶端（AP）表面结合，并引发宿主细胞的根本变化，从而允许细菌内化。在此期间，我们发现PA诱导AP表面的形态发生显著的局部变化，形成由基底外侧（BL）成分组成的膜状突起。这个突起很可能是细菌进入的通道。AP膜局部特性的这种深刻转变是PA对上皮细胞单层作用的第一个已知形态学标志。基于我们的数据，我们假设PA可以利用粘膜屏障上皮极性的小缺陷来引发一系列导致正反馈回路的事件，从而诱导AP膜转化为BL膜的显著形态学变化。形成具有新生AJ特征的突起，其充当细菌进入的管道。通过操纵上皮细胞极性，PA能够增强其细菌结合和进入，可能是通过增加宿主细胞受体或其他促进内化的因子的呈递。我们的目标是（1）确定TJ和AJ的哪些关键调节和结构成分被募集到突起中。(2)确定突起形成和细菌进入之间的时间和功能关系。(3)进行机制研究，以揭示PA如何劫持宿主细胞囊泡运输，以重新定向这些连接和BL组件的AP表面。(4)确定突出形成的细菌决定因素。这些研究将全面剖析PA与宿主细胞上皮之间的相互作用。他们将确定细菌用来致病的宿主因素。利用病原体研究哺乳动物生物学中的基本过程，例如上皮极性的建立和维持，除了发病机制之外，还对许多领域具有广泛的影响，包括癌症和发育生物学。此外，这些宿主细胞因子可以作为开发抗菌治疗剂的新靶标;因为药物靶向宿主而不是细菌分子，所以与常规抗菌治疗相比，它们不太可能产生耐药性。