The role of CFTR during macrophage-mediated killing of bacteria

CFTR 在巨噬细胞介导的细菌杀伤过程中的作用

• 批准号: 10369720
• 负责人: Benjamin T Kopp
• 金额: $ 38.48万
• 依托单位: RESEARCH INST NATIONWIDE CHILDREN'S HOSP
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-04-01 至 2022-08-18
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10369720
• 关键词: AKT inhibition; Antibiotic Therapy; Antibiotics; Autophagocytosis; Autophagosome; Bacteria; Bacterial Infections; Burkholderia cepacia; CRISPR/Cas technology; Chronic; Chronic Granulomatous Disease; Clinical; Cysteamine; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Data; Defect; Functional disorder; Genetic; Genetic Diseases; Goals; Host Defense; Human; Immune System Diseases; Immune response; Immune system; Immunologic Deficiency Syndromes; Impairment; Infection; Inflammation; Ions; Knock-out; Knowledge; Lead; Life; Lung; Lung diseases; Lung infections; Mediating; Mission; Mutate; Mutation; NADPH Oxidase; Outcome; PTEN gene; Pathway interactions; Pharmaceutical Preparations; Pharmacology; Production; Proteins; Proto-Oncogene Proteins c-akt; Pseudomonas aeruginosa; Public Health; Publishing; Reactive Oxygen Species; Research; Role; Signal Pathway; Signal Transduction; Signaling Protein; Sputum; Staphylococcus aureus; Techniques; Testing; Therapeutic; Translating; United States National Institutes of Health; Virulent; Work; chronic infection; combat; cystic fibrosis infection; cystic fibrosis patients; drug resistant pathogen; endoplasmic reticulum stress; functional loss; improved; innovation; macrophage; misfolded protein; monocyte; novel; novel therapeutic intervention; pathogen; prevent; protein aggregation; protein misfolding; recruit; response; restoration; targeted treatment; therapeutic development

PROJECT SUMMARY Why patients with cystic fibrosis (CF) continue to suffer from chronic bacterial infections despite new medications that improve CF transmembrane conductance regulator (CFTR) function is not known. The long-term goal is to develop therapeutics that modulate host immune responses in CF patients to mitigate chronic infection and inflammation. The objective of this proposal is to define how CFTR regulates macrophage function. The rationale underlying this proposal is that our prior work demonstrates that CF macrophages are integral to the inability of patients with CF to clear bacterial infections through failed NADPH oxidase (NOX) assembly and reduced autophagy. The central hypothesis is that loss of functional CFTR in human MΦs inhibits NOX assembly and subsequent ROS-mediated autophagy, independent of CFTR mutation class, but worsened by specific opportunistic bacteria. Further, we expect that a critical threshold of CFTR function is needed to reverse the NOX assembly/autophagy deficits and can be re-established by CFTR modulators combined with alternative CFTR restoration agents such as cysteamine or our novel autophagy stimulator, AR-13. The central hypothesis will be tested by pursuing three specific aims: 1) Define the mechanism by which CFTR regulates MΦ NOX assembly; 2) Determine how CF specific pathogens differentially regulate MΦ ROS production; 3) Determine the extent to which novel therapeutic approaches alter the MΦ NOX/autophagy axis. We will pursue these aims using an innovative combination of genetic and pharmacologic techniques in human macrophages. The proposed research is significant because a precise understanding of how CF macrophage function is regulated would allow novel antibiotic- and CFTR mutation- agnostic treatment approaches to infection. It is also significant because it will determine if specific pathogens independently contribute to deficits in macrophage-mediated bacterial killing. The expected outcome of this work will establish a mechanistic framework to enable us to target and correct defective CF MΦ-mediated bacterial killing. Ultimately, we will translate this new knowledge into a new treatment paradigm that uses innovative host-directed therapies to combat bacterial infections.

项目总结