Dissecting the Impact of Autophagy Regulators on Melanogenesis in Normal Human Ce
Dissecting the Impact of Autophagy Regulators on Melanogenesis in Normal Human Ce
批准号:
7777307
负责人:
Anand K Ganesan
金额:
$6.84万
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:
2009-03-01 至 2011-12-31
关键词:
Age related macular degenerationAnabolismAuditoryAutophagocytosisAutophagosomeBiochemicalBiologicalBiological AssayBiological ProcessCellsChloasmaCoupledDiseaseElectron MicroscopyEukaryotic CellEventEyeFibroblastsGene TargetingGenesHumanIn VitroIndividualLabyrinthLibrariesLysosomesMeasuresMelaninsMelanogenesisMelanoma CellMelanosomesMethodsModelingMonitorNeurologicNeuronsNormal CellNormal tissue morphologyOrganellesParkinson DiseasePathogenesisPathway interactionsPhysiologicalPigmentsProcessProductionProteinsRegulationRegulator GenesRoleScreening procedureSkinSmall Interfering RNAStructureSystemValidationVitiligoWaardenburg syndromeabstractingbasecell behaviordefined contributionfunctional genomicsgenome-widein vivoinsightkeratinocyteloss of functionmelanocytenervous system disordernovelpublic health relevanceskin disordersoundtherapeutic genetherapeutic targettraffickingultraviolet irradiation
中文摘要
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英文摘要
DESCRIPTION (provided by applicant):
Abstract Melanin protects the skin and eyes from the harmful effects of UV irradiation, protects neural cells from toxic insults, and is required for sound conduction in the inner ear. Aberrant regulation of melanogenesis underlies skin disorders (melasma and vitiligo), neurologic disorders (Parkinson's disease), auditory disorders (Waardenburg's syndrome), and opthalmologic disorders (age related macular degeneration). Extensive studies have identified over 150 genes that regulate melanin production in human cells, but have not yet yielded a complete understanding of the pathogenesis of disorders of melanin production. Recently, we combined a high-throughput cell-based one-well/one-gene screening platform with a genome-wide arrayed synthetic library of chemically synthesized small interfering RNAs to identify 94 novel regulators of melanogenesis in human cells. Secondary validation of gene targets identified using this functional genomics approach revealed that the approach had a low-false positive and off-target rate. Intriguingly, several components of the autophagy pathway were identified as novel regulators of melanin production in this analysis. Detailed validation of these putative autophagy regulators revealed that these genes impacted melanogenesis both in vitro and in vivo. In this proposal, we define the mechanism by which autophagy regulatory genes control pigment production in human skin. Initial studies will validate whether these putative autophagy regulators impact both melanin production and autophagy in MNT-1 cells and normal melanocytes. A defined approach will be utilized to determine the impact of depletion of autophagy regulators on the delivery of specific cargo to the melanosome. Biochemical approaches will be utilized to identify melanosome components that interact with novel autophagy regulators. Finally, a human skin equivalent model will be utilized to determine the contribution of individual autophagy regulators to melanin production in human skin. Through these studies, we hope to determine how the melanocyte utilizes the autophagy machinery to deliver specific protein cargo to the melanosome in vivo.
PUBLIC HEALTH RELEVANCE:
Project Narrative (relevance) Melanin protects the skin, eyes, and neurologic system from toxic insults and is aberrantly regulated in skin disorders (melasma and vitiligo), neurologic disorders (Parkinson's disease), auditory disorders (Waardenburg's syndrome) and opthalmologic disorders (age related macular degeneration). Genome-wide siRNAi-based functional genomics recently determined that several known and putative autophagy regulators impact melanogenesis in human cells. In this proposal, we determine how regulators of autophagy also impact melanin production. Through these studies we will gain insight into the regulation of vesicular trafficking in melanocytes and how these processes impact melanogenesis.
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科研奖励(0)
会议论文
Identifying Therapeutic Targets for Stage III Melanoma
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批准号:10520052
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项目类别:
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资助金额:$52.5万
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财政年份:2019
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负责人:Anand K Ganesan
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依托单位:
Identifying Therapeutic Targets for Stage III Melanoma
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PAK Kinases Regulate Melanoma Chemoresistance and Metastasis
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财政年份:2013
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依托单位:
Phosphoinositide Signaling Regulates Melanogenesis
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批准号:8826025
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PAK Kinases Regulate Melanoma Chemoresistance and Metastasis
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资助金额:$9.67万
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财政年份:2013
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依托单位:
Phosphoinositide Signaling Regulates Melanogenesis
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批准号:8456852
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资助金额:$33.2万
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财政年份:2013
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依托单位:
Phosphoinositide Signaling Regulates Melanogenesis
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资助金额:$38.0万
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PAK Kinases Regulate Melanoma Chemoresistance and Metastasis
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Phosphoinositide Signaling Regulates Melanogenesis
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PAK Kinases Regulate Melanoma Chemoresistance and Metastasis
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依托单位:
Aldehyde dehydrogenase: A novel regulator of melanin biogenesis
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依托单位:
Dissecting the Impact of Autophagy Regulators on Melanogenesis in Normal Human Ce
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资助金额:$6.99万
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依托单位:
Aldehyde dehydrogenase: A novel regulator of melanin biogenesis
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资助金额:$8.98万
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依托单位:
Aldehyde dehydrogenase: A novel regulator of melanin biogenesis
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批准号:8068672
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项目类别:
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资助金额:$12.39万
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财政年份:2009
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负责人:Anand K Ganesan
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依托单位:
Aldehyde dehydrogenase: A novel regulator of melanin biogenesis
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资助金额:$12.39万
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财政年份:2009
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负责人:Anand K Ganesan
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依托单位:
海外基金