Integrated Islet Distribution Program (U24) - 2021
综合胰岛分布计划 (U24) - 2021
基本信息
- 批准号:10681287
- 负责人:
- 金额:$ 298.35万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2012
- 资助国家:美国
- 起止时间:2012-09-30 至 2026-07-31
- 项目状态:未结题
- 来源:
- 关键词:AlgorithmsAmericanBasic ScienceBiological AssayBiomedical ResearchBusinessesCadaverCaringCitiesCommunicationCommunications MediaCommunitiesCountryCustomDataDevelopmentDiabetes MellitusDiseaseDrug or chemical Tissue DistributionElectronicsEnsureEquityFeesFosteringFunctional disorderFundingFutureGeneticGenetic RiskGenotypeGoalsGrantHumanIndividualInformaticsInvestmentsIslets of LangerhansLaboratoriesMaintenanceMedical Care CostsMissionModelingMonitorMusNational Institute of Diabetes and Digestive and Kidney DiseasesNon-Insulin-Dependent Diabetes MellitusNotificationPancreasPathologyPeer ReviewPersonsPhenotypePilot ProjectsPoliciesPreparationPreventionProceduresProcessProductionProtocols documentationProviderPublicationsQualifyingRare DiseasesRecommendationRecoveryReproducibilityResearchResearch PersonnelResourcesSamplingScienceScientistSecureServicesStandardizationSystemTechnologyTimeTissuesTrustUnited Network for Organ SharingUnited StatesUnited States National Institutes of HealthVisionWorkcostcost estimatedata integrationdata repositoryexperienceimprovedinsightinterestinteroperabilityisletmeetingsnext generationnovelphenotypic dataprogramsquality assurancetooltrend
项目摘要
PROJECT SUMMARY / ABSTRACT
Human pancreatic islets are an essential research resource for research on the prevention, treatment, and
pathophysiology of diabetes mellitus. Recent data have highlighted important differences between murine and
human islets, substantiating the continued need for access to human islets, as the gold standard in diabetes
research. City of Hope (COH) is applying for this U24 renewal to remain as the Integrated Islet Distribution
Program Coordinating Center (IIDP CC) for the next 5 years, to continue to provide distribution of human
cadaveric islets and ancillary tissue for biomedical research to researchers worldwide. Our proposal leverages
the significant investment made by NIH over the last 19 years that has established and successfully maintained
the IIDP at COH. From qualification and auditing of high-quality Islet Isolation Centers (IICs), to forecasting,
tracking, and meeting the needs of investigators, since 2002 our experienced team has worked with 20 different
islet isolation laboratories to coordinate the distribution of over 330 million islet equivalents to more than 400
investigators across 16 countries since 2002, supporting 767 peer reviewed publications. Through this renewal
we will continue to subcontract with our 5 highly qualified IICs to isolate and distribute human islets and ancillary
tissue via our advanced electronic Islet Allocation System (IAS). We will continue to manage the review process
for islet receipt, pilot studies, and Opportunity Pool funding. We will further enhance our IAS to broadcast offers
online and notify approved waiting researchers of islet availability, in a fair, equitable and time sensitive manner.
IIDP will continue to maintain the existing cost recovery system through subscription fees collected from islet
researchers, which has garnered a total of $9,303,950 since the implementation of subscription fees to offset
the expenses of pancreatic processing for the IICs. We will continue to closely monitor and help to improve the
quality of islets distributed, through the continuation of the Human Islet Phenotyping Program (HIPP) that
conducts assays on a sample from each islet isolation. IIDP has just added a Human Islet Genotyping Initiative
(HIGI) to genotype each isolation as well. Phenotyping and genotyping data, as well as UNOS data, extensive
donor and islet isolation data, will be made available to approved investigators through online access to the IIDP
Research Data Repository, with IIDP and NIDDK approval of applying scientists. Investigators can easily search
the required data, select filter criteria, save their searches, and download the integrated IIDP data for exploratory
analyses. Through our proven state-of-the-art administrative, business, technical, statistical, quality assurance,
and informatics processes and tools, the accessibility of human islets for investigators conducting essential
diabetes mellitus research will be secured. We will continue to provide an indispensable research resource for
the diabetes research community by ensuring that the IIDP remains stable, technologically advanced, continually
enhanced, and fully responsive to the islet needs of the research community, promoting the next generation of
scientific experimentation toward the prevention and treatment of diabetes.
项目摘要/摘要
人胰岛是预防、治疗和治疗糖尿病的重要研究资源。
糖尿病的病理生理学。最近的数据突显了小鼠和小鼠之间的重要差异
人类胰岛,证实继续需要进入人类胰岛,作为糖尿病的黄金标准
研究。希望之城(COH)正在申请将这一U24更新保留为综合岛屿分布
计划协调中心(IIDP CC)在未来5年内继续提供人力资源分配
身体胰岛和辅助组织供世界各地的研究人员进行生物医学研究。我们的提案充分利用了
NIH在过去19年中所做的重大投资已经建立并成功地维持了
COH的IIDP。从高质量的胰岛隔离中心(IICS)的资格认证和审核,到预测,
跟踪和满足调查人员的需求,自2002年以来,我们经验丰富的团队已与20个不同的
胰岛隔离实验室协调将3.3亿多个等量的胰岛分配给400多个
自2002年以来,来自16个国家的调查人员为767份同行评审的出版物提供了支持。通过此次更新
我们将继续与我们的5个高质量的IICS分包,以隔离和分发人类胰岛和附属
组织通过我们先进的电子胰岛分配系统(IAS)。我们将继续管理审查过程
用于小岛收据、试点研究和机会池资金。我们将进一步加强我们的IAS以广播报价
在网上,以公平、公平和对时间敏感的方式,通知经批准的等待研究人员可获得胰岛。
资讯基建发展计划会继续维持现有的成本回收制度,向小岛收取订阅费。
研究人员,自实施订阅费以来共获得9,303,950美元,以抵消
IICS的胰腺加工费用。我们会继续密切监察和协助改善
通过人类胰岛表型鉴定计划(HIPP)的延续,分发的胰岛质量
对每个胰岛分离的样本进行化验。IIDP刚刚增加了人类小岛基因分型倡议
(High)对每个分离株也进行基因分型。表型和基因分型数据,以及联合国操作系统的数据,内容广泛
捐赠者和胰岛隔离数据将通过IIDP的在线访问提供给经批准的调查人员
研究数据库,申请科学家获得IIDP和NIDDK批准。调查人员可以轻松地搜索
所需数据,选择筛选条件,保存他们的搜索,并下载集成的IIDP数据以供探索
分析。通过我们经过验证的最先进的管理、业务、技术、统计、质量保证,
和信息学过程和工具,人类小岛的可及性对于调查人员进行
糖尿病研究将得到保障。我们将继续为以下项目提供不可或缺的研究资源
糖尿病研究界通过确保IIDP保持稳定、技术不断进步
增强并充分响应研究社区的小岛需求,促进下一代
预防和治疗糖尿病的科学实验。
项目成果
期刊论文数量(77)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Advances in Pancreatic Islet Transplantation Sites for the Treatment of Diabetes.
- DOI:10.3389/fendo.2021.732431
- 发表时间:2021
- 期刊:
- 影响因子:5.2
- 作者:Cayabyab F;Nih LR;Yoshihara E
- 通讯作者:Yoshihara E
Calcineurin/NFATc2 and PI3K/AKT signaling maintains β-cell identity and function during metabolic and inflammatory stress.
- DOI:10.1016/j.isci.2022.104125
- 发表时间:2022-04-15
- 期刊:
- 影响因子:5.8
- 作者:Darden CM;Vasu S;Mattke J;Liu Y;Rhodes CJ;Naziruddin B;Lawrence MC
- 通讯作者:Lawrence MC
SGLT2 is not expressed in pancreatic α- and β-cells, and its inhibition does not directly affect glucagon and insulin secretion in rodents and humans.
- DOI:10.1016/j.molmet.2020.101071
- 发表时间:2020-12
- 期刊:
- 影响因子:8.1
- 作者:Chae H;Augustin R;Gatineau E;Mayoux E;Bensellam M;Antoine N;Khattab F;Lai BK;Brusa D;Stierstorfer B;Klein H;Singh B;Ruiz L;Pieper M;Mark M;Herrera PL;Gribble FM;Reimann F;Wojtusciszyn A;Broca C;Rita N;Piemonti L;Gilon P
- 通讯作者:Gilon P
Adapting Physiology in Functional Human Islet Organogenesis.
- DOI:10.3389/fcell.2022.854604
- 发表时间:2022
- 期刊:
- 影响因子:5.5
- 作者:Yoshihara, Eiji
- 通讯作者:Yoshihara, Eiji
3-D physiomimetic extracellular matrix hydrogels provide a supportive microenvironment for rodent and human islet culture.
3-D生理模拟的细胞外基质水凝胶为啮齿动物和人类胰岛培养提供了支撑性的微环境。
- DOI:10.1016/j.biomaterials.2018.08.057
- 发表时间:2019-04
- 期刊:
- 影响因子:14
- 作者:Jiang K;Chaimov D;Patel SN;Liang JP;Wiggins SC;Samojlik MM;Rubiano A;Simmons CS;Stabler CL
- 通讯作者:Stabler CL
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Carmella Evans-Molina其他文献
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{{ truncateString('Carmella Evans-Molina', 18)}}的其他基金
β cell miRNAs Function as Molecular Hubs of Type 1 Diabetes Pathogenesis
β 细胞 miRNA 作为 1 型糖尿病发病机制的分子中心
- 批准号:
10561855 - 财政年份:2022
- 资助金额:
$ 298.35万 - 项目类别:
β cell miRNAs Function as Molecular Hubs of Type 1 Diabetes Pathogenesis
β 细胞 miRNA 作为 1 型糖尿病发病机制的分子中心
- 批准号:
10321295 - 财政年份:2021
- 资助金额:
$ 298.35万 - 项目类别:
Control of beta cell function and survival by RYR2-mediated calcium signals
通过 RYR2 介导的钙信号控制 β 细胞功能和存活
- 批准号:
10491304 - 财政年份:2021
- 资助金额:
$ 298.35万 - 项目类别:
β cell miRNAs Function as Molecular Hubs of Type 1 Diabetes Pathogenesis
β 细胞 miRNA 作为 1 型糖尿病发病机制的分子中心
- 批准号:
10615586 - 财政年份:2021
- 资助金额:
$ 298.35万 - 项目类别:
Control of beta cell function and survival by RYR2-mediated calcium signals
通过 RYR2 介导的钙信号控制 β 细胞功能和存活
- 批准号:
10689291 - 财政年份:2021
- 资助金额:
$ 298.35万 - 项目类别:
Control of beta cell function and survival by RYR2-mediated calcium signals
通过 RYR2 介导的钙信号控制 β 细胞功能和存活
- 批准号:
10375087 - 财政年份:2021
- 资助金额:
$ 298.35万 - 项目类别:
Indiana University clinical Center for acute pancreatitis and diabetes clinical research network
印第安纳大学急性胰腺炎和糖尿病临床中心临床研究网络
- 批准号:
10673629 - 财政年份:2020
- 资助金额:
$ 298.35万 - 项目类别:
Indiana University clinical Center for acute pancreatitis and diabetes clinical research network
印第安纳大学急性胰腺炎和糖尿病临床中心临床研究网络
- 批准号:
10458720 - 财政年份:2020
- 资助金额:
$ 298.35万 - 项目类别:
Indiana University clinical Center for acute pancreatitis and diabetes clinical research network
印第安纳大学急性胰腺炎和糖尿病临床中心临床研究网络
- 批准号:
10265585 - 财政年份:2020
- 资助金额:
$ 298.35万 - 项目类别:
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