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Genetic Dissection of Drosophila Hematopoiesis

Genetic Dissection of Drosophila Hematopoiesis
果蝇造血的遗传解剖
批准号:
8644130
负责人:
UTPAL BANERJEE
金额:
$37.73万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-05-10 至 2015-12-31

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中文摘要
翻译
描述(由申请人提供):从理解正常功能和白血病的角度来看,血液发育和疾病的分子机制具有极大的兴趣和重要性。果蝇长期以来一直作为许多发育过程的遗传模型,但其作为造血模型的有用性直到最近才被认识到。维持果蝇造血干细胞的机制在发育和功能策略上与哺乳动物系统具有显著的保守性。这项工作旨在确定维持干细胞稳态的分子途径。还提出了系统信号和营养剥夺对骨髓细胞发育的作用。这些都是发育和医学相关的问题,模型系统服从遗传筛选是必不可少的发展。该提案有四个具体目标。在目标1中,将开发一种稳态模型,通过该模型,血液前体不仅通过来自小生境的信号维持,而且还通过来自已开始分化的细胞的信号维持。在目标2中,将研究转录因子STAT在果蝇干细胞命运维持中的参与。在目标3中,将研究控制干细胞完整性的细胞外基质组分的作用。在最后的目标中,将研究来自控制果蝇血液干细胞维持的大脑的信号,并研究它们在饥饿诱导的干细胞损失中的作用。
英文摘要
DESCRIPTION (provided by applicant): Molecular mechanisms underlying blood development and disorders are of great interest and importance from the perspective of understanding normal function and leukemias. Drosophila has long served as a genetic model for many developmental processes, but its usefulness as a hematopoietic model has only recently been appreciated. The mechanisms that maintain blood stem cells in Drosophila show remarkable conservation in strategy of development and function with mammalian systems. The proposed work intends to determine the molecular pathways that maintain stem cell homeostasis. Also proposed is the role of systemic signals and nutrient deprivation on myeloid cell development. These are developmentally and medically relevant problems for which model systems amenable to genetic screens are essential to develop. The proposal has four specific aims. In Aim 1, a homeostatic model by which blood precursors are maintained not only by a signal from a niche, but also from the cells that have started differentiating will be developed. In Aim 2, the involvement of the transcription factor STAT in the maintenance of stem cell fate in Drosophila will be investigated. In Aim 3, the role of extracellular matrix components that control the integrity of stem cells will be studied. In the final aim, signals arising from the brain that control blood stem cell maintenance in Drosophila will be investigated and their role in starvation induced stem cell loss studied.
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