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Molecular Pathology of HIV/SIV Enteropathy

Molecular Pathology of HIV/SIV Enteropathy
HIV/SIV 肠病的分子病理学
批准号:
8293149
负责人:
Mahesh Mohan
金额:
$35.11万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-07-01 至 2015-06-30
关键词:
AcidsAcuteAddressAffectAntibodiesBacteriaBindingBiological AssayCCAAT-Enhancer-Binding ProteinsCCR5 geneCD3 AntigensCD4 Positive T LymphocytesCardiacCell CountCell physiologyCellsChronicCloningCodeColonComplementComplexConfocal MicroscopyDataDiagnosisDiagnosticDiarrheaDiseaseDisease ProgressionEnteralEpithelialEpithelial CellsEpitheliumEventExcisionFollow-Up StudiesFunctional disorderFutureGastrointestinal DiseasesGastrointestinal tract structureGene ExpressionGene ProteinsGene TargetingGenesGenetic TranscriptionGoalsHIVHIV EnteropathyHeart DiseasesHistopathologyImmuneImmune systemImmunofluorescence ImmunologicImmunohistochemistryIn Situ HybridizationIn VitroIndividualInfectionInfiltrationInflammationInflammatoryInterleukin-6Intestinal MucosaIntestinesIntravenousJanus kinaseLamina PropriaLeadLong Terminal RepeatsLymphocyteMacacaMacaca mulattaMass Spectrum AnalysisMessenger RNAMetabolic DiseasesMethodologyMicroRNAsMolecularMolecular ProfilingNeurologicNucleotidesOperative Surgical ProceduresOpportunistic InfectionsPathogenesisPathway interactionsPatientsPatternPlasmaPlasma CellsPlayProductionProteinsProteomeRNARNA InterferenceRegulator GenesReportingReverse Transcriptase Polymerase Chain ReactionRoleSIVSTAT proteinSTAT3 geneSmall RNASpecimenStagingStructureT-Cell DepletionTestingTherapeuticTight JunctionsTimeTissuesTransfectionTranslational RepressionUntranslated RNAViralViral Load resultbasecancer typecell typecytokineend stage diseaseexperiencegastrointestinalgastrointestinal functiongastrointestinal symptomgenome-widehuman diseaseimmune activationimprovedinsightintestinal epitheliumlocked nucleic acidmacrophagememory CD4 T lymphocytemolecular pathologyneoplasticnervous system disordernovelp65protein expressionpublic health relevanceresponseskin disordertranscription factorwasting

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DESCRIPTION (provided by applicant): The gastrointestinal (GI) tract is a major target of HIV/SIV infection and CD4+ T cell depletion. The damage to the mucosal immune system is associated with a variety of GI manifestations collectively called AIDS enteropathy; generally characterized by chronic diarrhea, and wasting. Although our understanding of HIV/SIV enteropathy has greatly improved lately, the recent discovery of microRNAs (miRNAs) has added yet another novel and complex regulator of gene expression with potential roles in the molecular pathogenesis of this disorder. miRNAs are ~21-23 nucleotide noncoding RNAs, highly conserved and suppress gene expression by targeting mRNAs for translational repression or degradation. While miRNA studies are being reported extensively in various types of cancer, and at increasing rates in cardiac, neurological, metabolic and skin diseases, their role in idiopathic GI disorders such as HIV/SIV enteropathy is unknown and yet to be addressed. Preliminary Locked Nucleic Acid-based miRNA microarray profiling of colon tissue from SIV-infected macaques with chronic diarrhea and wasting revealed significant deregulation in the expression of several miRNAs. Based on our strong preliminary evidence, we hypothesize that miRNA expression is deregulated in the GI tract consequent to HIV/SIV infection and that this contributes to disruption of enteric structure and function (AIDS enteropathy). The broad goals of this study are to 1a.) Identify genome wide temporal changes in miRNA expression (microarray and miRNA cloning) in the GI tract in response to SIV infection and determine if expression signatures specific to pathogenic events such as immune activation, inflammation, and epithelial barrier disruption can be identified 1b.) Further corroborate all miRNAs showing differential expression using real-time RT-PCR. 1c.) Determine cellular localization of differentially expressed miRNAs (in situ hybridization/immunofluorescence) in the colon and verify if differences in expression exist between cell types in close proximity 2.) Determine the functional significance of the inflammation associated miR-212 by validating its putative protein targets (mass spectrometry) in the intestinal epithelium and in in vitro cultured primary intestinal macrophages. Understanding the role of miRNAs and their putative target genes/proteins will provide important insights into the pathogenesis of HIV/SIV enteropathy and, possibly, other GI inflammatory conditions. Molecular mechanisms uncovered through these studies may open new miRNA-based strategies for the diagnosis and treatment of idiopathic GI disorders like AIDS enteropathy. PUBLIC HEALTH RELEVANCE: The proposed study for the first time will investigate the role of small regulatory ribonucleic acids (microRNAs) in the pathogenesis of HIV/SIV enteropathy. HIV/SIV enteropathy is an idiopathic disorder that affects two-thirds of HIV infected patients and the exact causes still remain obscure. Studies of this kind will further enhance our understanding of the molecular pathogenesis of this order and will help develop better diagnostic and therapeutic strategies in the future.
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Cannabinoid modulation of EV composition and function in HIV/SIV infection
  • 批准号:
    10662831
  • 项目类别:
  • 资助金额:
    $77.6万
  • 财政年份:
    2022
  • 负责人:
    Mahesh Mohan
  • 依托单位:
Cannabinoid modulation of EV composition and function in HIV/SIV infection
  • 批准号:
    10693315
  • 项目类别:
  • 资助金额:
    $78.47万
  • 财政年份:
    2022
  • 负责人:
    Mahesh Mohan
  • 依托单位:
Characterizing the physicochemical properties of membraneless condensates and its regulation by delta-9-tetrahydrocannabinol in HIV/SIV infection.
  • 批准号:
    10664337
  • 项目类别:
  • 资助金额:
    $21.8万
  • 财政年份:
    2021
  • 负责人:
    Mahesh Mohan
  • 依托单位:
Characterizing the physicochemical properties of membraneless condensates and its regulation by delta-9-tetrahydrocannabinol in HIV/SIV infection.
  • 批准号:
    10842560
  • 项目类别:
  • 资助金额:
    $44.06万
  • 财政年份:
    2021
  • 负责人:
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  • 依托单位:
海外基金