Genetic analysis of stem cell maintenance in vivo

体内干细胞维持的遗传分析

• 批准号: 7921521
• 负责人: SEAN J MORRISON
• 金额: $ 37.26万
• 依托单位: UNIVERSITY OF MICHIGAN AT ANN ARBOR
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-08-24 至 2013-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7921521
• 关键词: Alleles; Angiopoietin-1; Binding; Blood Cells; Blood Vessels; Bone Marrow; Breeding; CXCL12 gene; Cell Cycle; Cell Lineage; Cell Maintenance; Cell physiology; Cells; Data; Defect; Endosteal Cell; Endothelial Cells; Growth Factor; Hematopoiesis; Hematopoietic stem cells; Injury; Life; Maintenance; Megakaryocytes; Membrane; Mus; Osteoblasts; Partner in relationship; Pericytes; Physiological; Regulation; Source; Stem Cell Factor; Stem cells; Supporting Cell; Surface; Testing; Tissues; cell motility; cell type; design; genetic analysis; in vivo; promoter; public health relevance; recombinase; research study; self-renewal; stem cell niche

DESCRIPTION (provided by applicant): Hematopoietic stem cells (HSCs) persist throughout life and dynamically regulate their numbers after injury by undergoing self-renewing divisions that depend upon both cell- intrinsic and cell-extrinsic mechanisms. With respect to cell-extrinsic mechanisms, HSCs are thought to reside within specialized microenvironments created by supporting cells in the bone marrow that express membrane-bound and secreted factors that promote HSC maintenance (survival and self-renewal), and that regulate HSC migration, quiescence, and differentiation. Many bone marrow HSCs reside at, or near, the osteoblasts at the endosteal surface and osteoblasts have been proposed to secrete a number of factors that promote HSC maintenance. Many HSCs also reside adjacent to sinusoidal blood vessels in the bone marrow, and vascular or perivascular cells have also been proposed to secrete factors that regulate HSC maintenance. Nonetheless, none of these factors have ever been conditionally deleted from any candidate niche cell. As a result, the physiological sources of these factors have never been tested in functional experiments. Angiopoietin-1 (Ang-1), Stem Cell Factor (SCF), and CXCL12 are all genetically required for maintenance of normal numbers of HSCs but none of these factors have been conditionally deleted from osteoblasts or from vascular/perivascular cells to identify the biologically important source(s) of these factors. Ultimately, it will not be possible to identify the cells that create HSC niches without genetically identifying the cells that secrete factors required for HSC maintenance. Our preliminary expression data suggest that megakaryocytes are the major source of Ang-1 in the bone marrow and that there are multiple sources of SCF including both endothelial cells and endosteal cells. To test which cells are functionally important sources of these factors for HSC maintenance we have generated floxed alleles of Ang-1 and Scf and propose to mate mice bearing these alleles with mice expressing Cre-recombinase under the control of promoters specific to osteoblasts, megakaryocytes, and endothelial cells. These experiments will also test whether a single cell type is the main source of multiple factors required for HSC maintenance or whether different cell types produce different factors that regulate HSCs. This will provide the first functional test of which cells regulate HSC maintenance in vivo. PUBLIC HEALTH RELEVANCE: This project is designed to assess which cells are the physiologically important sources of growth factors that are critical for the maintenance and regulation of hematopoietic stem cells. This will provide important new information regarding the identities of the cells that constitute the hematopoietic stem cell niche in vivo. Such information is critical to understand how blood cell formation is regulated and how stem cells are sustained in this tissue throughout life.

描述（由申请人提供）：造血干细胞（HSC）在整个生命过程中持续存在，并通过依赖于细胞内在和细胞外在机制的自我更新分裂在损伤后动态调节其数量。关于细胞外源性机制，HSC被认为存在于由骨髓中的支持细胞产生的特殊微环境中，所述骨髓中的支持细胞表达促进HSC维持（存活和自我更新）的膜结合和分泌因子，并且调节HSC迁移、静止和分化。许多骨髓HSC位于或靠近骨内膜表面的成骨细胞，并且已提出成骨细胞分泌许多促进HSC维持的因子。许多HSC也存在于骨髓中的窦状血管附近，并且血管或血管周围细胞也被提出分泌调节HSC维持的因子。尽管如此，这些因素中没有一个曾经被有条件地从任何候选生态位细胞中删除。因此，这些因素的生理来源从未在功能实验中进行过测试。血管生成素-1（Ang-1）、干细胞因子（SCF）和CXCL 12都是维持正常数量的HSC在遗传上所需的，但这些因子都没有从成骨细胞或血管/血管周细胞中有条件地删除，以确定这些因子的生物学重要来源。最终，如果不从遗传学上鉴定出分泌HSC维持所需因子的细胞，就不可能鉴定出产生HSC小生境的细胞。我们的初步表达数据表明，巨核细胞是骨髓中Ang-1的主要来源，SCF有多种来源，包括内皮细胞和骨内膜细胞。为了测试哪些细胞是HSC维持的这些因子的功能重要来源，我们产生了Ang-1和Scf的floxed等位基因，并建议将携带这些等位基因的小鼠与在成骨细胞、巨核细胞和内皮细胞特异性启动子控制下表达Cre重组酶的小鼠交配。这些实验还将测试单个细胞类型是否是HSC维持所需的多种因子的主要来源，或者不同的细胞类型是否产生调节HSC的不同因子。这将提供第一个功能测试的细胞调节HSC的维持在体内。 公共卫生相关性：该项目旨在评估哪些细胞是对造血干细胞的维持和调节至关重要的生长因子的生理重要来源。这将提供重要的新的信息，关于构成造血干细胞龛在体内的细胞的身份。这些信息对于了解血细胞形成是如何调节的以及干细胞如何在整个生命过程中维持在这个组织中至关重要。