Human 3D Microtissues for Toxicity Testing via Integrated Imaging, Molecular and Functional Analyses
通过集成成像、分子和功能分析进行人体 3D 微组织毒性测试
基本信息
- 批准号:9352553
- 负责人:
- 金额:$ 76.16万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2017
- 资助国家:美国
- 起止时间:2017-09-15 至 2022-07-31
- 项目状态:已结题
- 来源:
- 关键词:3-DimensionalAddressAdverse effectsAnimalsBioinformaticsBiologicalBiological AssayBiologyBiomedical EngineeringBiometryBrainCell CommunicationCell physiologyCellsCharacteristicsComplexComputer SimulationDataDatabasesDevelopmentDoseEngineeringEvaluationFacultyGoalsGoldHealthHeartHumanImageImage AnalysisIn VitroLaboratoriesLungMathematicsMeasuresMedicineMethodsModelingMoldsMolecularMolecular and Cellular BiologyMorphologyNational Institute of Environmental Health SciencesNational Research CouncilOrganOrganismOutcomeOvaryPaperPathologyPathway interactionsPhasePopulationProstatePublic HealthPublishing Peer ReviewsReaction TimeRecruitment ActivityReporterReportingReproducibilityResearchResearch Project GrantsRisk AssessmentSafetyStructureSystemSystems BiologyTechniquesTechnologyTestingTimeTissuesToxicant exposureToxicity TestsToxicologyUncertaintyUniversitiesUpdateValidationVisionbasecommercializationcostcost effectivedesignenvironmental chemicalhistopathological examinationhuman tissueimprovedin vitro testingin vivoinnovationmembernew technologynext generationnovelprofessorreconstructionresponsetooltoxicant
项目摘要
PROJECT SUMMARY
Historically, toxicity testing has relied on high dose exposures in animals with default methods for
extrapolating to low level exposures in human populations, producing (at high cost) great uncertainty for
human health risk assessments. This Brown University Bioengineering Research Partnership (BRP)—Human
3D Microtissues for Toxicity Testing via Integrated Imaging, Molecular and Functional Analyses—
implements a transformative change by developing novel 3D human microtissues as a bridging technology
based on integrating imaging, molecular and functional analyses that will facilitate more rapid, cost-effective
toxicity testing of environmental chemicals and emerging toxicants.
The project has two phases. Phase 1 establishes 3D microtissues of five tissue types (prostate, ovary,
lung, brain, heart) to address the key challenges facing development of these predictive biology platforms:
reproducibility, biological complexity, integrated endpoints, and human variability. Phase 2 selects two of these
3D microtissue models for computational systems biology analysis with sufficient dose- and time-response
data to define adverse points of departure for an in vitro-to-in vivo extrapolation and safety assessment.
Working with collaborators and commercial partners, the BRP team includes faculty from biology,
engineering, mathematics, and medicine who have formed the Center to Advance Predictive Biology
(https://www.brown.edu/research/projects/center-to-advance-predictive-biology/). The following working
hypothesis guides the project: In vitro pathology assessment of human 3D microtissues within a
computational systems biology framework identifies toxicant-induced adverse points of departure for safety
assessment. The high content, high throughput platforms for these evaluations are 3D microtissue test
systems that re-capitulate the differentiated features and characteristic cellular functions of humans tissues.
Progress toward the goal of transforming toxicity testing will be made by addressing these Specific Aims:
Specific Aim 1. Innovate the 3D microtissue platform with engineering solutions for improved well
designs, confocal imaging, and high-throughput workflows
Specific Aim 2. Optimize 3D microtissues as predictive biology platforms
Specific Aim 3. Streamline image acquisition, reconstruction, and quantitative analysis for the in vitro
pathology assessment of 3D microtissues
Specific Aim 4. Integrate imaging, molecular, and functional endpoints within a computational systems
biology framework for the purpose of human safety assessment
This Brown University BRP will accelerate development and commercialization of human 3D
microtissue platforms as alternatives to animal toxicity testing.
项目总结
项目成果
期刊论文数量(0)
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{{ truncateString('KIM BOEKELHEIDE', 18)}}的其他基金
Human 3D Microtissues for Toxicity Testing via Integrated Imaging, Molecular and Functional Analyses
通过集成成像、分子和功能分析进行人体 3D 微组织毒性测试
- 批准号:
10240515 - 财政年份:2017
- 资助金额:
$ 76.16万 - 项目类别:
Identification of Molecular Biomarkers in Rat Sperm and Testis Exposed to BPA
暴露于 BPA 的大鼠精子和睾丸中分子生物标志物的鉴定
- 批准号:
8478105 - 财政年份:2011
- 资助金额:
$ 76.16万 - 项目类别:
Identification of Molecular Biomarkers in Rat Sperm and Testis Exposed to BPA
暴露于 BPA 的大鼠精子和睾丸中分子生物标志物的鉴定
- 批准号:
8686849 - 财政年份:2011
- 资助金额:
$ 76.16万 - 项目类别:
Identification of Molecular Biomarkers in Rat Sperm and Testis Exposed to BPA
暴露于 BPA 的大鼠精子和睾丸中分子生物标志物的鉴定
- 批准号:
8334560 - 财政年份:2011
- 资助金额:
$ 76.16万 - 项目类别:
Identification of Molecular Biomarkers in Rat Sperm and Testis Exposed to BPA
暴露于 BPA 的大鼠精子和睾丸中分子生物标志物的鉴定
- 批准号:
8230312 - 财政年份:2011
- 资助金额:
$ 76.16万 - 项目类别:
Formative Center for the Evaluation of Environmental Impacts on Fetal Development
环境对胎儿发育影响评估中心
- 批准号:
7827476 - 财政年份:2010
- 资助金额:
$ 76.16万 - 项目类别:
Project 2: Human Fetal Prostate and Endocrine Disruption
项目2:人类胎儿前列腺与内分泌干扰
- 批准号:
7846629 - 财政年份:2010
- 资助金额:
$ 76.16万 - 项目类别:
Molecular Mechanism of Human Fetal Testis Susceptibility to Endocrine Disruption
人胎儿睾丸易受内分泌干扰的分子机制
- 批准号:
8013324 - 财政年份:2010
- 资助金额:
$ 76.16万 - 项目类别:
Molecular Mechanism of Human Fetal Testis Susceptibility to Endocrine Disruption
人胎儿睾丸易受内分泌干扰的分子机制
- 批准号:
7784697 - 财政年份:2010
- 资助金额:
$ 76.16万 - 项目类别:
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