首页--医药、卫生论文--肿瘤学论文--消化系肿瘤论文--肝肿瘤论文

肝脏巨噬细胞天然免疫膜受体的表达与肝癌的相关性研究

摘要第5-10页
ABSTRACT第10-15页
Symbols and Abbreviations第22-23页
Chapter 1:Literature Review第23-43页
    1.1 The liver第23-25页
    1.2 Cellular components of the liver第25-33页
        1.2.1 Resident and infiltrating macrophages第26-29页
            1.2.1.1 Heterogeneity of macrophages第26-27页
            1.2.1.2 Macrophages and chronic liver disease第27-28页
            1.2.1.3 Macrophages and liver fibrosis第28-29页
            1.2.1.4 Macrophages and HCC第29页
        1.2.2 NK cells第29-31页
        1.2.3 NKT cells第31-33页
    1.3 Co-inhibitory receptors第33-38页
        1.3.1 CD200-CD200R axis第36-38页
    1.4 Scavenger receptors第38-43页
        1.4.1 MARCO第40-43页
Chapter 2:Materials and Methods第43-59页
    2.1 Materials第43-46页
        2.1.1 Patients and specimens第43页
        2.1.2 Cell lines and cell culturing reagents第43页
        2.1.3 Reverse transcription and real-time PCR第43-44页
        2.1.4 FACS第44-45页
        2.1.5 PBMC isolation第45页
        2.1.6 Immunohistochemical staining第45-46页
        2.1.7 Immunofloresence第46页
    2.2 Equipments第46-47页
    2.3 Methods第47-59页
        2.3.1 Cell culturing第47-50页
            2.3.1.1 Reagents preparation第47-48页
            2.3.1.2 Cell recovering第48页
            2.3.1.3 Cell sub-culturing第48-50页
            2.3.1.4 Cell freezing第50页
            2.3.1.5 Cell numbering第50页
        2.3.2 Reverse transcription and real-time PCR第50-52页
            2.3.2.1 Total RNA extraction第50-51页
            2.3.2.2 Reverse transcription第51-52页
            2.3.2.3 Real-time PCR第52页
        2.3.3 PBMC isolation第52-53页
            2.3.3.1 Reagents preparation第52-53页
            2.3.3.2 PBMC isolation第53页
        2.3.4 FACS第53-55页
            2.3.4.1 Reagents preparation第53-54页
            2.3.4.2 Staining cell surface antigens第54页
            2.3.4.3 Staining intracellular antigens第54-55页
        2.3.5 Immunohistochemical staining第55-57页
            2.3.5.1 Reagents preparation第55页
            2.3.5.2 Deparaffinization and rehydration第55页
            2.3.5.3 Epitope retrival第55-56页
            2.3.5.4 Immunohistochemical staining第56-57页
            2.3.5.5 Signal detection,counterstain,dehydration,clearing,and mounting第57页
        2.3.6 Immunofloresence第57-58页
        2.3.7 Softwares and Statistical analysis第58-59页
            2.3.7.1 Evaluation of IOD/area第58页
            2.3.7.2 Statistical analysis第58-59页
Chapter 3:CD200R predicts the prognosis of human hepatocellular carcinoma第59-77页
    3.1 Introduction第59-61页
        3.1.1 Liver and HCC第59页
        3.1.2 Immune responses and immune tolerance第59页
        3.1.3 Immune escape and immunotherapy第59-60页
        3.1.4 CD200 and CD200 receptor第60-61页
    3.2 Results第61-71页
        3.2.1 CD200R and CD200 were positively correlated in peritumoural stroma and intratumoural regions第61-63页
        3.2.2 CD200R and CD200 were mainly expressed in the peritumoural stroma of HCC tissues第63-65页
        3.2.3 CD200R expression accumulated along tumor progression第65-67页
        3.2.4 CD200R was predominantly expressed by infiltrating macrophages and positively associated with liver injury第67-70页
        3.2.5 Density of CD200R in peritumoural stroma predicted elevated recurrence and reduced survival in HCC patients第70-71页
    3.3 Discussion and Conclusions第71-77页
        3.3.1 CD200R and autoimmune diseases第71-72页
        3.3.2 CD200R and various carcinoma第72-73页
        3.3.3 CD200R and HCC第73-74页
        3.3.4 CD200R and HCC immunotherapy第74-75页
        3.3.5 Conclusions and prospection第75-77页
Chapter 4:Decreased expression of MARCO is associated with the progressionand prognosis of human hepatocellular carcinoma第77-93页
    4.1 Introduction第77-79页
        4.1.1 Anti-inflammatory roles of MARCO第77-78页
        4.1.2 Pro-inflammatory roles of MARCO第78页
        4.1.3 MARCO and HCC第78-79页
    4.2 Results第79-87页
        4.2.1 MARCO expression was down-regulated in the intratumoral tissues of HCC第79-81页
        4.2.2 Expression of MARCO declined with disease and tumour progression第81-84页
        4.2.3 MARCO~+ cells co-localized with CD68~+ cells under immunofluorescence第84-85页
        4.2.4 Density of MARCO in the intratumoural tissues predicted increased survival in HCC patients第85-87页
    4.3 Discussion and Conclusions第87-93页
        4.3.1 The liver and liver-resident macrophages第87页
        4.3.2 Scavenger receptors and the regulation of tumors第87-88页
        4.3.3 MARCO and HCC第88-90页
        4.3.4 Conclusions and prospection第90-93页
References第93-105页
Acknowledgements第105-107页
Publications and Awards第107-108页

论文共108页,点击 下载论文
上一篇:甘草及其成分促进Treg细胞的产生与功能及单倍体干细胞M期观察的研究
下一篇:NKp30~+ NK细胞参与Peg-IFN-α-2b治疗慢性乙型肝炎中HBV病毒的清除