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Differential Gene Expression of Inflammatory Signaling in Localized Aggressive Periodontitis BY WHITNEY DUNN WEINER Specialty Certificate in Periodontics, University of Illinois at Chicago College of Dentistry, 2013 D.D.S., University of Iowa College of Dentistry, 2010 B.A., The Colorado College, 2005 THESIS Submitted as partial fulfillment of the requirements for the degree of Master of Science in Oral Sciences in the Graduate College of the University of Illinois at Chicago, 2013 Chicago, Illinois Thesis Committee Dr. Thomas C. Hart, Chair Dr. Joseph V. Califano, East Carolina University Dr. Christopher G. Engeland This thesis is dedicated to my parents, Greg and Wendy Dunn, and my husband, S. Eliot Weiner, for their unconditional support and encouragement. ii ACKNOWLEDGEMENTS I would like to thank my mentor, Dr. Thomas Hart, for his patience, unwavering support, confidence, unparalleled knowledge, and constant encouragement. He provided guidance and helped me achieve my research goals. I would also like to thank my thesis committee members, Dr. Califano and Dr. Engeland, for their support and assistance. Additionally, I would like to thank Dr. Shujuan Guo for all of her hard work culturing cells and isolating RNA. This thesis would not have been possible without the encouragement and flexibility from my full-time faculty in the Department of Post-Graduate Periodontics and University of Illinois at Chicago College of Dentistry. Particularly, a special thanks to my program director, Dr. Saba Khan, and my clinical director, Dr. Praveen Gajendrareddy. . WDW iii TABLE OF CONTENTS CHAPTER PAGE 1. INTRODUCTION 1.1 Background …………………………………………………… 1 1.2 Significance …………………………………………………… 8 1.3 Specific Aims …………………………………………………… 9 1.4 Hypotheses …………………………………………………… 10 2. REVIEW OF LITERATURE 2.1 Classification of Periodontal Diseases…………………………. 11 2.2 Prevalence of Periodontitis………………………………………. 13 2.3 The Genetic Basis of AP……………………………………… 14 2.4 Role of the Early Innate Immune Response in Periodontitis... 32 3. METHODOLOGY 3.1 Study Design …………………………………………………… 49 3.2 Materials and Methods ……………………………………….. 49 3.3 Statistical Analysis …….……………………………………….. 52 3.4 IRB/ACC Approval …….……………………………………….. 52 4. RESULTS 4.1 Results ………………………………………………………….. 53 5. DISCUSSION 5.1 Discussion ………………………………………………………. 62 5.2 Limitations of the Study ……………………………………….. 72 5.3 Future Research ……………………………………………….. 74 6. CONCLUSION ………………………………………………………... 77 iv TABLE OF CONTENTS (continued) PAGE CITED LITERATURE ……………………………………………….. 78 APPENDICES APPENDIX A …………………………………………………. 96 APPENDIX B …………………………………………………. 97 APPENDIX C …………………………………………………. 98 APPENDIX D ………………………………………………… 99 APPENDIX E …………………………………………………. 101 APPENDIX F …………………………………………………. 102 APPENDIX G …………………………………………………. 105 APPENDIX H …………………………………………………. 106 APPENDIX I …………………………………………………. 107 APPENDIX J …………………………………………………. 108 APPENDIX K …………………………………………………. 111 VITA ………………………………………………………………….. 113 v LIST OF TABLES TABLE PAGE I. SINGLE NUCLEOTIDE POLYMORPHISMS REPORTED TO BE ASSOCIATED WITH AP……………………………………………….. 37 II. 20 GENES ASSOCIATED WITH THE EARLY INNATE IMMUNE RESPONSE AND THE PRIMARY FUNCTION OF EACH GENE ACCORDING TO STRING DATABASE (VERSION 9.0) …………… 43 vi LIST OF FIGURES FIGURE PAGE 1. STRING analysis (version 9.0) of 20 candidate early innate immune response genes indicating directionality and mode of action……….. 48 2. Gene Expression Following Stimulation with IL-1β…………………... 54 3. Gene Expression Following Stimulation with IL-1β…………………... 56 4. Gene Expression Following Stimulation with PgLPS………………… 57 5. Gene Expression Following Stimulation with PgLPS………………… 58 6. Gene Expression Following Stimulation with AaLPS………………… 59 7. Gene Expression Following Stimulation with AaLPS……………….... 60 vii LIST OF ABBREVIATIONS AaLPS Actinobacillus actinomycetemcomitans LPS AAP American Academy of Periodontology ACTB actin, beta AD Autosomal Dominant AP Aggressive Periodontitis APCS Amyloid P component, serum AR Autosomal Recessive C3 Complement component 3 CASP1 Caspase 1, apoptosis-related cysteine peptidase CD4 CD4 molecule CD8a CD8a molecule CD14 CD14 molecule CD40 CD40 molecule, TNF receptor superfamily member 5 CCL2 Chemokine (C-C motif) ligand 2 Also called Monocyte chemoattractant protein- 1(MCP-1) CCL3 Chemokine (C-C motif) ligand 3 CDC Centers for Disease Control CTSC Cathepsin C CP Chronic Periodontitis CRP C-reactive protein, pentraxin-related viii LIST OF ABBREVIATIONS (continued) CSF2 Colony stimulating factor 2 (granulocyte- macrophage) CXCL8 Interleukin-8 (IL-8) DDX58 DEAD (Asp-Glu-Ala-Asp) box polypeptide 58 DEFB1 Defensin, beta 1 DNAS DNA Services EOP Early Onset Periodontitis FAM5C Family with sequence similarity 5, member C FCGR Fc fragment of IgG, gamma receptor FPR Formyl peptide receptor GAP Generalized Aggressive Periodontitis GJP Generalized Juvenile Periodontitis GWAS Genome Wide Association Studies HGP Human Genome Project HLA Major histocompatibility complex, class II HLA-DRA Major histocompatibility complex, class II, DR alpha IFNA1 interferon, alpha 1 IFNA2 interferon, alpha 2 IFNG Interferon gamma IL1 Interleukin 1 IL1A Interleukin 1 alpha (IL-1α) IL1B Interleukin 1 beta (IL-1β) ix LIST OF ABBREVIATIONS (continued) IL1RN Interleukin 1 receptor antagonist IL2 Interleukin 2 IL4 Interleukin 4 IL6 Interleukin 6 IL8 Interleukin 8 IL10 Interleukin 10 IL12 Interleukin 12 IL13 Interleukin 13 IL17 Interleukin 17 IL18 Interleukin 18 IRAK1 Interleukin-1 receptor-associated kinase 1 IRB Institutional Review Board IRF3 Interferon regulatory factor 3 IRF7 Interferon regulatory factor 7 ITGAM Integrin, alpha M (complement component 3 receptor 3 subunit) JE Junctional Epithelium JP Juvenile Periodontitis LAD Leukocyte Adhesion Deficiency LAP Localized Aggressive Periodontitis LD Linkage Disequilibrium LJP Localized Juvenile Periodontitis LPS Lipopolysaccharide x

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In 1989, the American Academy of Periodontology (AAP) replaced the . cytokines and chemokines but also the absence of anti-inflammatory mediator recruitment, a clinical hallmark of the disease (Ryu et al., 2007) revolutionize human and medical genetics by providing fundamental insight into.
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