High-resolution 3D in situ Spatial Gene Expression Profiling Technology for Human Brain Specimens

人脑标本高分辨率3D原位空间基因表达谱分析技术

基本信息

  • 批准号:
    10385072
  • 负责人:
  • 金额:
    $ 50万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2022
  • 资助国家:
    美国
  • 起止时间:
    2022-09-01 至 2024-08-31
  • 项目状态:
    已结题

项目摘要

Project Title: High-resolution 3D in situ Spatial Gene Expression Profiling Technology for Human Brain Specimens Project Description The overall aim of this Phase I project is to apply Expansion Sequencing, a genome-wide in situ transcriptomics profiling technology with unprecedented spatial resolution in 3D, to human brain tissues to empower brain disease research and therapeutic development. Neurodegenerative diseases, such as Alzheimer’s disease affects over 11% of the population aged above 65, causing ⅓ of death in seniors, and costs hundreds of billions of dollars a year. Yet, no disease modifying therapeutics have been approved for marketing. The ability to obtain data and validate discoveries directly in human samples is paramount to our ability to characterize and understand brain disorders. Spatially resolved transcriptomics, helps scientists understand how the different cells are organized, using fluorescence microscopy imaging has shown unmatched promise in characterizing different cell types in native tissue, change during development and aging, and how they influence behavior and disease. However, many of existing spatial technologies are limited to thin animal brain sections. They are bound by optical diffraction-limited resolution, restraining the ability to precisely define a large variety of cell types organized in 3D. Tissues from humans and those with neurodegenerative disease have high degree of autofluorescence caused by protein aggregates (such as Amyloid plaques), lipofuscin granules and dense vessels. Recently published in Science, Expansion Sequencing (ExSeq) is the first in situ genome-wide 3D spatial gene expression profiling technology. It provides unprecedented imaging resolution in 3D using thick mouse brain sections. This allows for clear definition of synapse junctions and mapping gene transcripts with single- and sub-cellular precision, which had not been possible with conventional fluorescence confocal microscopes used by most researchers. In order to make ExSeq suitable for human studies and commercially available, we identified and tested a new set of methods that will allow us to optimise ExSeq for human specimens, and improve sensitivity and specificity. We are building a set of analytical tools to help visualize, debug and improve the robustness of the analytics pipeline. We have also obtained access to a wide variety of precious human brain tissues, to help us test different sample preparation conditions and validate our methods. For this Phase I project, we will develop ExSeq protocol for human brain tissue characterisation with a proof-of-concept gene panel, and create a robust image processing and analytical pipeline that can accommodate images generated from different experimental and laboratory settings. Finally, we will process and analyse a set of human normal and Alzheimer’s diseased brain tissues, and validate results against published data and prior research. Building upon a strong scientific foundation supported with publications, we are bringing together extensive expertise in protocol optimization and sequencing technology for ExSeq and deep knowledge of Alzheimer’s and neurodegenerative disease pathology to make it an impactful tool for both basic science and therapeutic research and development.
项目名称:高分辨率3D原位空间基因表达谱技术 人脑标本 项目描述 该第一阶段项目的总体目标是应用扩展测序, 具有前所未有的空间分辨率的全基因组原位转录组学分析技术 以 3D 方式对人类脑组织进行研究,以促进脑部疾病的研究和治疗开发。 超过 11% 的人口患有神经退行性疾病,例如阿尔茨海默病 65岁以上的老年人,造成⅓的老年人死亡,每年造成数千亿美元的损失。 然而,尚未有任何疾病修饰疗法获得批准上市。 直接在人类样本中获取数据并验证发现对于我们的能力至关重要 表征和理解大脑疾病的空间解析转录组学,有助于 科学家使用荧光显微镜了解不同细胞的组织方式 成像在表征天然组织中不同细胞类型方面显示出无与伦比的前景, 发育和衰老过程中的变化,以及它们如何影响行为和疾病。 然而,许多现有的空间技术仅限于薄薄的动物大脑切片。 它们受到光学衍射极限分辨率的限制,限制了精确定义的能力 以 3D 形式组织的多种细胞类型。 神经退行性疾病具有由蛋白质聚集体引起的高度自发荧光 (如淀粉样斑块)、脂褐素颗粒和致密血管最近发表于。 Science,扩展测序 (ExSeq) 是第一个原位全基因组 3D 空间基因 它使用厚层提供前所未有的 3D 成像分辨率。 小鼠大脑切片可以清晰地定义突触连接和绘制基因图谱。 具有单细胞和亚细胞精度的转录本,这是不可能的 大多数研究人员使用传统的荧光共焦显微镜。 ExSeq 适合人类研究并可商业化,我们鉴定并测试了一种新的 一组方法将使我们能够优化人类样本的 ExSeq,并改进 我们正在构建一套分析工具来帮助可视化、调试和分析。 提高分析管道的稳健性我们还获得了广泛的访问权限。 多种珍贵的人体脑组织,帮助我们测试不同的样品制备条件 并验证我们的方法。 对于这个一期项目,我们将为人脑组织开发 ExSeq 协议 使用概念验证基因面板进行表征,并创建强大的图像处理和 分析管道,可以容纳从不同的实验和生成的图像 最后,我们将处理和分析一组人体正常和 阿尔茨海默病患病脑组织,并根据已发表的数据和之前的数据验证结果 建立在出版物支持的强大科学基础上,我们正在 汇集了协议优化和测序技术方面的丰富专业知识 ExSeq 和对阿尔茨海默病和神经退行性疾病病理学的深入了解 它是基础科学和治疗研究与开发的有效工具。

项目成果

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Mahender Babu Dewal其他文献

Mahender Babu Dewal的其他文献

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