The Cytoskeletal System in Preservation Injury
The Cytoskeletal System in Preservation Injury
批准号:
8330293
负责人:
Martin J. MANGINO
金额:
$30.71万
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:
2010-09-30 至 2014-08-31
关键词:
AddressAntibodiesAreaAttenuatedBindingBiochemicalBiological PreservationCell Culture TechniquesCell LineCell Membrane StructuresCell modelCellsClinicalComplexControl GroupsCryopreservationCytoprotectionCytoskeletal ProteinsCytoskeletonDataEnd stage renal failureEngineeringEpithelial CellsEtiologyFailureFamily suidaeFutureGenesGoalsHarvestHealthHumanInjuryInjury to KidneyIschemiaKidneyKidney TransplantationKnock-in MouseKnowledgeMembraneMetabolicMitochondriaModelingMolecularMolecular ConformationMolecular GeneticsMonitorMusMutant Strains MiceMutationNephronsOrganOrgan HarvestingsOrgan PreservationOrgan TransplantationOutcomePathway interactionsPatientsPeptide HydrolasesPhenotypePhosphorylationPhosphotransferasesPhysiologicalProteinsReadingRecombinantsRenal tubule structureReperfusion InjuryReperfusion TherapyRho-associated kinaseRoleSiteStructural ProteinSystemTechniquesTestingTherapeuticTransgenic OrganismsTranslationsTransplantationWaiting Listscell typeclinically relevantezrinhigh riskimprovedinhibitor/antagonistinjuredinnovationinsightkidney cellkidney preservationknock-downmitochondrial membranemutantnew therapeutic targetnovelpublic health relevancetherapeutic target
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Kidney transplantation is the only viable treatment for patients with end stage renal failure. However, the severe organ shortage leaves thousands in the US to suffer and die on waiting lists. Expanding the donor pool to include high risk donors may solve this shortage if those grafts could be preserved properly. However, organ preservation injury that is suffered after organ harvest is not well understood and little major advancement have been made in this area in the last 20 years. Therefore, the objective of this proposal is to identify novel molecular mechanisms of renal preservation injury involving the cytoskeleton system and to use this knowledge to direct future therapeutic approaches. Preliminary data show that the cytoskeleton protein ezrin fails during renal cold storage and that augmenting expression of ezrin significantly protects renal tubule epithelial cells from preservation injury. Conversely, ezrin knock-down does the opposite, which suggests causation. This proposal will test likely mechanisms of ezrin-induced cytoprotection in cell and kidney cold storage injury models by using molecular and genetic approaches to alter ezrin functionality. These studies will determine if ezrin, in its proper configuration, protects cell membrane structure and preserves cell mitochondrial function during cold ischemia and reperfusion. Renal epithelial cell models will be used where the cells express different amounts of wild type and mutant ezrin protein. Higher order models of preservation injury using isolated renal tubules and whole kidneys derived from transgenic ezrin knock-in mice expressing mutant ezrin genes will also be used. At the end of these studies, we will have gathered useful molecular information of how ezrin is involved in cold storage renal preservation injury and if this involvement is clinically relevant. These insights, together with previously identified mechanisms, may suggest likely therapeutic targets to improve renal preservation, which will allow harvesting of less robust kidneys from high risk donors to help alleviate the donor shortage.
PUBLIC HEALTH RELEVANCE: Kidney transplantation is the treatment of choice for patients in end stage renal failure but there are not enough usable donor kidneys available. This need to expand the donor pool has increased the need to understand how to better preserve organs for transplantation, which in turn requires a more complete understanding of the mechanisms of organ preservation injury. This proposal is relevant to human health because it will bridge some of the key knowledge gaps in our understanding of the basic molecular mechanisms of how kidneys are injured after they are removed from the donor. This will reveal novel therapeutic targets to focus treatments and help alleviate the donor shortage.
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会议论文
Polymer use in Preservation of Tissue Perfusion to Address Sepsis
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批准号:10325345
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项目类别:
-
资助金额:$25.65万
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财政年份:2021
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负责人:Martin J. MANGINO
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依托单位:
The Cytoskeletal System in Preservation Injury
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批准号:8537435
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项目类别:
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资助金额:$29.64万
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财政年份:2010
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负责人:Martin J. MANGINO
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依托单位:
The Cytoskeletal System in Preservation Injury
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批准号:8152215
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项目类别:
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资助金额:$30.71万
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财政年份:2010
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负责人:Martin J. MANGINO
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依托单位:
The Cytoskeletal System in Preservation Injury
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批准号:8040211
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项目类别:
-
资助金额:$37.38万
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财政年份:2010
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负责人:Martin J. MANGINO
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依托单位:
MEDIATORS OF INTESTINAL ISCHEMIA
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批准号:2182445
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项目类别:
-
资助金额:$9.33万
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财政年份:1992
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负责人:Martin J. MANGINO
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依托单位:
MEDIATORS OF INTESTINAL ISCHEMIA
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批准号:3468111
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项目类别:
-
资助金额:$10.12万
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财政年份:1992
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负责人:Martin J. MANGINO
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依托单位:
MEDIATORS OF INTESTINAL ISCHEMIA
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批准号:2182446
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项目类别:
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资助金额:$9.84万
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财政年份:1992
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负责人:Martin J. MANGINO
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依托单位:
MEDIATORS OF INTESTINAL ISCHEMIA
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批准号:3468110
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项目类别:
-
资助金额:$10.63万
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财政年份:1992
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负责人:Martin J. MANGINO
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依托单位:
MEDIATORS OF INTESTINAL ISCHEMIA
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批准号:2182444
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项目类别:
-
资助金额:$9.04万
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财政年份:1992
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负责人:Martin J. MANGINO
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依托单位:
海外基金