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NADPH氧化酶p40phox亚基在小鼠抗细菌感染中的作用机理研究

致谢第10-12页
Abstract第12-15页
摘要第16-19页
缩略词第19-22页
Chapter Ⅰ:Literature Review第22-63页
    1 Interaction between Salmonella Infection and Host Defense第22-33页
        1.1 Overview of Salmonella第22页
        1.2 Virulence Mechanisms第22-24页
        1.3 Salmonella Infection第24-26页
            1.3.1 Local Mucosal Invasion of Salmonella第24-26页
            1.3.2 Systemic Dissemination of Salmonella第26页
        1.4 Host Defense第26-28页
            1.4.1 Detection of Salmonella by PRRs第26-27页
            1.4.2 Ampliation of The Inflammatory Response第27-28页
            1.4.3 Phagocytes Infiltration第28页
        1.5 Conclusion第28-29页
        References第29-33页
    2 The Role of NADPH Oxidase in Host Defense第33-48页
        2.1 Overview of NADPH Oxidase第33页
        2.2 The NOX Family第33-38页
            2.2.1 Phagocyte NADPH Oxidase第34-35页
            2.2.2 NOX2 Homologues第35-36页
            2.2.3 Regulatory Subunits第36-38页
        2.3 NADPH Oxidase-derived ROS第38-39页
        2.4 Host Defense and Inflammation第39-42页
            2.4.1 Microbicidal Activity第39-40页
            2.4.2 Immune Modulatory Effects第40-42页
        References第42-48页
    3 The Role of Autophagy in Salmonella Infection第48-62页
        3.1 Overview of Autophagy第48-50页
        3.2 Interaction between Salmonella and Antibacterial Autophagy第50-56页
            3.2.1 Salmonella Is Targeted for Antibacterial Autophagy第50-55页
            3.2.2 Salmonella Manipulates Autophagy第55-56页
        3.3 Conclusion第56-57页
        References第57-62页
    4 Aims and Objectives第62-63页
Chapter Ⅱ:Methology and Data Analysis第63-151页
    1 The Role of p40~(phox) in Host Defense against Systemic Salmonella Infection第63-93页
        1.1 Introduction第63-64页
        1.2 Materials and Methods第64-74页
            1.2.1 Mice第64页
            1.2.2 Reagents第64-65页
            1.2.3 Laboratory Equipment第65-66页
            1.2.4 Methods第66-74页
        1.3 Data Analysis and Findings第74-90页
            1.3.1 p40~(phox) deficiency increases mortality and bodyweight changes of mice during Salmonella infection第74-75页
            1.3.2 p40~(phox) deficiency exacerbates bacterial translocation in Salmonella-infected mice第75-76页
            1.3.3 p40~(phox-/-) mice develop more severe spleen and liver inflammation after oral S. Typhimurium infection第76-79页
            1.3.4 p40~(phox) deficiency in S. Typhimurium-infected mice enhances the recruitment of macrophages and neutrophils after oral infection第79-82页
            1.3.5 p40~(phox) deficiency in S. Typhimurium-infected mice upregulates the expression of chemoattractants in spleens after oral infection第82-83页
            1.3.6 p40~(phox) deficiency in S. Typhimurium-infected mice increases the CD4~+ T cells recruitment after oral infection第83-84页
            1.3.7 p40~(phox) deficient mice exhibit normal ability to recruit phagocytes to the peritoneal cavity after intra-peritoneal infection with Salmonella第84-86页
            1.3.8 p40~(phox) deficiency exacerbates tissue inflammation and bacterial translocation in Salmonella-infected mice after intra-peritoneal infection第86-88页
            1.3.9 p40~(phox) deficiency in S. Typhimurium-infected mice enhances the recruitment of macrophages and neutrophils to spleen after intra-peritoneal infection第88-90页
        1.4 Discussion第90-91页
        References第91-93页
    2 The Role of p40~(phox) in Regulating Intestinal Inflammation Caused by SalmonellaInfection第93-112页
        2.1 Introduction第93页
        2.2 Materials and Methods第93-97页
            2.2.1 Mice第93-94页
            2.2.2 Reagents第94页
            2.2.3 Laboratory Equipment第94页
            2.2.4 Methods第94-97页
        2.3 Data Analysis and Findings第97-108页
            2.3.1 p40~(phox) deficiency exacerbates Salmonella-induced mucosal injury第97-98页
            2.3.2 p40~(phox) deficiency alters the distribution of specific junctional proteins in cecal epithelium in Salmonella-infected mice第98-100页
            2.3.3 p40~(phox) deficiency exacerbates bacterial translocation in Salmonella-infected mice第100-101页
            2.3.4 p40~(phox) deficiency in 5. Typhimurium-infected mice regulates the expression of mucins and enzymes involved in glycan modifications第101-104页
            2.3.5 Pretreatment with streptomycin induces intense intestinal inflammation in Salmonella-infected mice第104-105页
            2.3.6 p40~(phox) deficiency in S. Typhimurium-infected mice enhances the recruitment of macrophages and neutrophils in intestinal mucosa第105-107页
            2.3.7 p40~(phox) deficiency in S. Typhimurium-infected mice alters the distribution of macrophages and neutrophils in intestinal mucosa第107-108页
        2.4 Discussion第108-110页
        References第110-112页
    3 The Role of p40~(phox) in Regulating Antimicrobial Activity of Macrophages第112-129页
        3.1 Introduction第112-113页
        3.2 Materials and Methods第113-117页
            3.2.1 Mice第113页
            3.2.2 Reagents第113-114页
            3.2.3 Laboratory Equipment第114页
            3.2.4 Methods第114-117页
        3.3 Data Analysis and Findings第117-125页
            3.3.1 p40~(phox-/-) macrophages exhibit normal bacterial phagocytosis and reduced bactericidal activity第117-119页
            3.3.2 p40~(phox-/-) macrophages and p40~(phox-/-) neutrophils exhibit severe defects in PMA-induced ROS production第119-120页
            3.3.3 p40~(phox-/-) macrophages have compromised autophagic killing of Salmonella第120-123页
            3.3.4 p40~(phox-/-) macrophages produce an elevated amount of IL-1β induced by Samonella antigen stimulation and exhibit enhanced inflammasome activation第123-125页
        3.4 Discussion第125-127页
        References第127-129页
    4 The Role of p40~(phox) in Host Defense against Citrobacter rodentium Infection第129-151页
        4.1 Introduction第129-130页
        4.2 Materials and Methods第130-134页
            4.2.1 Mice第130页
            4.2.2 Reagents第130-131页
            4.2.3 Laboratory Equipment第131页
            4.2.4 Methods第131-134页
        4.3 Data Analysis and Findings第134-143页
            4.3.1 p40~(phox) deficiency does not increase susceptibility of mice to C. rodentium infection第134-135页
            4.3.2 p40~(phox) deficiency does not exacerbate C. rodentium-induced colonic pathology第135-137页
            4.3.3 Differential cytokine expression in C. rodentium-infected p40~(phox) -deficient mice第137-139页
            4.3.4 p40~(phox) deficiency alters inflammatory cell infiltration of the colonic mucosa第139-140页
            4.3.5 Altered cytokine production in p40~(phox) -deficient mice with C. rodentium infection第140-142页
            4.3.6 p40~(phox) deficiency increases iNOS expression and NO production in response to C. rodentium infection第142-143页
        4.4 Discussion第143-147页
        References第147-151页
Chapter Ⅲ:Conclusion and Future Work第151-152页
    1 Concluding Statements第151页
    2 Suggested Future Work第151-152页
个人简历第152-153页

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