Organ Specific Project - Bone Marrow

器官特定项目 - 骨髓

基本信息

  • 批准号:
    10251351
  • 负责人:
  • 金额:
    $ 44.04万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2020
  • 资助国家:
    美国
  • 起止时间:
    2020-09-01 至 2022-08-31
  • 项目状态:
    已结题

项目摘要

PROJECT SUMMARY – BONE ORGAN SPECIFIC PROJECT The bone is a highly complex organ made of three tissue types with distinct functions, including cells from hematopoietic, mesenchymal and endothelial lineages. Confined within one organ and thoroughly mixed with each other, these three tissues are mutually dependent for their development and homeostasis. The spatial organization of the various cell types and their cross-talk in the bone is a major gap of our knowledge. The goal of the bone Organ Specific Project (B-OSP) is to address this knowledge gap and generate high quality, single- cell resolution, longitudinal imaging and multi-omics data of normal bones across the human lifespan. We propose the following three specific aims: 1) To refine protocols for biospecimen processing, multi-omics and imaging assays and define inter-individual variability using our existing banked bone samples. Using existing biobanked normal bones from the autopsy program, we will perform a series of pilot studies to refine our protocols for biospecimen collection and processing, as well as single-cell omics and imaging assays. 2) To procure, archive, and annotate high-quality normal bone samples across human life span. We have established a streamlined procurement and biorepository infrastructure to support our bone OSP. We will procure normal bone from the same donor of 6 age groups across the human life span. 3) To spatially profile bone specimens across the human life span using a set of robust and scalable imaging and single-cell omics assays. We will use micro computed tomography to image every bone we collect at both the macroscale and mesoscale. At the microscale, we will perform single-nucleus RNA sequencing (snRNA-Seq) and single-cell assay for transposase-accessible chromatin using sequencing (scATAC-Seq) of two strategic anatomical sites per bone to determine cell type composition, as well as transcriptional and epigenetic signatures. We will perform multiplexed error-robust fluorescence in situ hybridization (MERFISH, for transcriptomics) and Co- Detection by Indexing (CODEX, for proteomics) analyses.
项目摘要-骨器官专项项目

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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KATHRIN M BERNT其他文献

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{{ truncateString('KATHRIN M BERNT', 18)}}的其他基金

IDP mediated transcriptional stabilization as a cause of AML
IDP 介导的转录稳定是 AML 的一个原因
  • 批准号:
    10419497
  • 财政年份:
    2022
  • 资助金额:
    $ 44.04万
  • 项目类别:
A stalled chromatin regulatory network that mediates the oncogenic activity of Meningioma-1
介导 Meningioma-1 致癌活性的停滞染色质调控网络
  • 批准号:
    10579293
  • 财政年份:
    2022
  • 资助金额:
    $ 44.04万
  • 项目类别:
A stalled chromatin regulatory network that mediates the oncogenic activity of Meningioma-1
介导 Meningioma-1 致癌活性的停滞染色质调控网络
  • 批准号:
    10445974
  • 财政年份:
    2022
  • 资助金额:
    $ 44.04万
  • 项目类别:
IDP mediated transcriptional stabilization as a cause of AML
IDP 介导的转录稳定是 AML 的一个原因
  • 批准号:
    10588195
  • 财政年份:
    2022
  • 资助金额:
    $ 44.04万
  • 项目类别:
Organ Specific Project - Bone Marrow
器官特定项目 - 骨髓
  • 批准号:
    10118853
  • 财政年份:
    2020
  • 资助金额:
    $ 44.04万
  • 项目类别:
Center for Developmental Mapping of Heart and Bone Tissues
心脏和骨组织发育图谱中心
  • 批准号:
    10251350
  • 财政年份:
    2020
  • 资助金额:
    $ 44.04万
  • 项目类别:
Center for Developmental Mapping of Heart and Bone Tissues
心脏和骨组织发育图谱中心
  • 批准号:
    10118850
  • 财政年份:
    2020
  • 资助金额:
    $ 44.04万
  • 项目类别:
The role of H3K79 methylation in IDH-mutant leukemia
H3K79 甲基化在 IDH 突变白血病中的作用
  • 批准号:
    9918256
  • 财政年份:
    2017
  • 资助金额:
    $ 44.04万
  • 项目类别:
The role of H3K79 methylation in IDH-mutant leukemia
H3K79 甲基化在 IDH 突变白血病中的作用
  • 批准号:
    9460182
  • 财政年份:
    2017
  • 资助金额:
    $ 44.04万
  • 项目类别:
The role of H3K79 methylation in IDH-mutant leukemia
H3K79 甲基化在 IDH 突变白血病中的作用
  • 批准号:
    9010300
  • 财政年份:
    2015
  • 资助金额:
    $ 44.04万
  • 项目类别:

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