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Tracking Hematopoiesis at the Single Cell Level

机译:在单个细胞层面跟踪血液缺陷

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Despite intensive research, many longstanding questions of experimental hematology remain unsolved. One major reason is the fact that hematopoiesis is usually followed by analyzing populations of cells rather than individual cells, at few points in time during an experiment and without knowing (or quickly loosing) the cells' individual identities. The static picture yielded by this approach makes it impossible to appreciate the dynamic developmental processes leading to the generation of the full hematopoietic system from individual hematopoietic stem cells (HSCs). Real-time tracking of individual cells in culture, tissues, or whole organisms would be an extremely powerful approach to fully understand the developmental complexity of hematopoiesis. To this end, a computer-aided culture and bioimaging system is being developed to follow the fate of individual cells over long periods of time. This system is used to follow the development of multilineage cobblestone colonies from adult HSCs in stroma cocultures at the single cell level over many generations. To facilitate noninvasive detection of lineage commitment in these cultures, new subcellular forms of optimized fluorescent proteins have been developed to allow simultaneous marking of multiple hematopoietic lineages within the same animal.
机译:尽管研究了密集的研究,但许多长期以来的实验血液学的问题仍未解决。一种主要原因是血缺陷通常在实验期间分析细胞而不是单个细胞的细胞而不是单个细胞的群体,而不知道(或快速丢失)细胞的个体身份。这种方法产生的静态图片使得不可能理解动态发育过程,导致来自个体造血干细胞(HSC)的全造血系统产生的。培养,组织或全生物中单个细胞的实时跟踪将是一种充分了解血液缺陷的发育复杂性的极其强大的方法。为此,正在开发一种计算机辅助文化和生物影像体系,在长时间内跟随各个电池的命运。该系统用于遵循在许多几代人的单细胞水平的基质共科培养中从成年HSCs中发育来自成年HSC的多层鹅卵石菌落。为了便于非侵入性检测这些培养物中的谱系承诺,已经开发出新的亚细胞形式的优化荧光蛋白形式,以便在同一动物内同时标记多种造血谱系。

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