The Role of Cholesterol in HIV Pathogenesis: Implications for NPC2
The Role of Cholesterol in HIV Pathogenesis: Implications for NPC2
批准号:
7678267
负责人:
Ebony Michelle Coleman
金额:
$3.55万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-08-15 至 2011-08-14
关键词:
AIDS/HIV problemAddressAffectBiogenesisCardiovascular systemCellsCholesterolCholesterol HomeostasisDataDiseaseDockingEnzyme-Linked Immunosorbent AssayFibroblastsFlow CytometryGene SilencingGenesGuanosine Triphosphate PhosphohydrolasesHIVHIV-1Integration Host FactorsLaboratoriesLipodystrophyMembrane MicrodomainsMicroscopyMissionModelingOrganellesParentsPathogenesisPharmaceutical PreparationsPlayProcessProductionProductivityProteinsPublic HealthReportingRoleStagingStudy modelsSupraoptic Vertical OphthalmoplegiaSyndromeT-LymphocyteTechniquesTestingTherapeuticViralViral PathogenesisVirionVirusWorkcholesterol traffickingdisease phenotypehealth disparityinsightlate endosomeoverexpressionprotein expressionprotein transportrab GTP-Binding Proteinsresearch studytrafficking
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英文摘要
DESCRIPTION (provided by applicant): Previous studies have shown that HIV-1 preferentially buds from cholesterol-rich microdomains called lipid rafts, and that cholesterol is required for HIV infectivity and structural integrity. Moreover, the presence of cholesterol is also required both for HIV entry into susceptible cells as well as for release of infectious virions. The viral requirement of cholesterol for HIV infectivity led us to study the relationship between HIV-1 budding and assembly and cholesterol trafficking. Niemann Pick Type C (NPC2) protein plays a vital role in the intracellular trafficking of cholesterol. Given the viral requirement of cholesterol for productivity and given the role of NPC2 in cholesterol trafficking, we hypothesize that NPC2 activity is required in the late stages of HIV-1 biogenesis. HIV-1 induced lipodystrophy and the consequent cardiovascular syndromes, as well as the critical role of cholesterol in viral pathogenesis, make this study highly relevant to NIH's mission to eliminate HIV/AIDS health disparities and to promote public health. The findings from this project may also offer insight into other cholesterol- associated disparities. To this end, the following specific aims have been developed: 1) To test whether or not NPC2 plays a role in HIV-1 replication. 2) To examine the mechanism by which cholesterol trafficking effects viral production using NPC disease as a model. The primary scientific techniques that will be utilized to address these aims are Western analysis, PCR, gene silencing, ELISA, flow cytometry, and microscopy.
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