Pancreas Organ Specific Project

胰腺器官特定项目

• 批准号: 10254373
• 负责人: ALVIN C POWERS
• 金额: $ 20.08万
• 依托单位: VANDERBILT UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-09-30 至 2024-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10254373
• 关键词: 3-Dimensional; Academic Medical Centers; Acinar Cell; Address; Analytical Chemistry; Atlases; Biological Assay; Blood Vessels; Cell physiology; Cells; Cellular Structures; Clinical; Collection; Complement; Complex; Cooperative Human Tissue Network; D Cells; Data; Data Analyses; Data Science; Digestion; Disease; Duct (organ) structure; Duodenum; Emerging Technologies; Endocrine; Endocrinology; Ensure; Environment; Enzymes; Excision; Exocrine pancreas; Extracellular Matrix; Eye; Food; Funding; G Cells; Gene Expression; Genetic Transcription; Glean; Glucagon; Goals; Health; Heterogeneity; Histologic; Human; Human BioMolecular Atlas Program; Human Characteristics; Human Resources; Image; Imaging Techniques; Immunofluorescence Immunologic; Individual; Insulin; Ions; Islets of Langerhans; Kidney; Knowledge; Link; Lipids; Maps; Mass Spectrum Analysis; Metabolic; Methods; Microscopy; Modality; Molecular; Molecular Profiling; Morphology; Multimodal Imaging; Multiomic Data; Normalcy; Operative Surgical Procedures; Organ; Output; Pancreas; Pancreatic Polypeptide; Preparation; Proteins; Quality Control; Research; Research Personnel; Resolution; Rodent; Sampling; Somatostatin; Source; Spatial Distribution; Specificity; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Speed; Stains; Standardization; Surface; Technology; Tissue Banks; Tissue imaging; Tissues; Transcript; United States National Institutes of Health; Work; base; blood glucose regulation; cell type; data quality; demographics; experimental study; extracellular; ghrelin; human imaging; imaging modality; improved; indexing; insight; instrumentation; islet; molecular imaging; multimodality; nutrient absorption; pancreas imaging; professor; reconstruction; single cell analysis; single cell technology; single-cell RNA sequencing; spatial relationship; three dimensional structure

PROJECT SUMMARY – Pancreas Organ Specific Project. Comprehensive 3-dimensional biomolecular analysis within tissues requires the coordination of data from many analytical technologies. We will develop a multimodal strategy to obtain spatially specific ‘omics’ information directly from human pancreas. This work will leverage the unique instrumentation capabilities and expertise of the Mass Spectrometry Research Center (MSRC) in which Professors Spraggins, Caprioli, Schey, Gutierrez and Van de Plas are key personnel. Building from previous work developing atlases of human kidney tissue, we will integrate ultra-high speed, high spatial resolution (<10μm) MALDI timsTOF IMS with high mass resolution (>40,000 Resolving Power, <2 ppm mass accuracy) for molecular imaging of human pancreata with an unprecedented combination of spatial fidelity and molecular specificity. The high-throughput capabilities of MALDI timsTOF IMS will be critical for generating high- spatial resolution 3-D molecular images from statistically relevant numbers of normal pancreas samples. MALDI IMS will provide the specificity and mass accuracy necessary to link ion images to orthogonal LC-based fragmentation experiments for molecular identification. Fragmentation will be performed using spatially specific surface sampling approaches to produce LC-MS/MS data from tissues in a manner that is compatible with IMS and capable of being integrated into HuBMAP tissue atlases. To maximize information gleaned from imaging experiments and lay the groundwork for data-driven image fusion and 3-D reconstruction outlined in the Data Analysis Core Research Strategy, we will also develop methods for collecting various microscopy-based image modalities (e.g. autofluorescence and stained microscopy) and pancreas specific, highly multiplexed immunofluorescence using CODEX. Through the use of our multimodal pipeline, we propose to map spatial relationships of pancreas cell types within healthy tissue across a multitude of demographics. Aim 1: To create a pancreas-specific biospecimen collection and management plan. Aim 2: To establish a pre-analytical pipeline for standardizing sample preparation, determining tissue normalcy, and providing quality control metrics. Aim 3: To develop a multimodal characterization pipeline for pancreas-specific 3-D molecular imaging. Aim 4: To scale and standardize pancreas-specific 3-D molecular imaging. To accomplish these aims, we have assembled a highly interactive and established team of investigators consisting of complementary expertise in endocrinology, analytical chemistry, and data science.

项目摘要-胰腺器官特异性项目。综合三维生物分子