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空间限制决定了造血干/祖细胞在体外的命运。

Space constraints govern fate of hematopoietic stem and progenitor cells in vitro.

机构信息

Max Bergmann Center of Biomaterials, Leibniz Institute of Polymer Research Dresden, Hohe Strasse 6, 01069 Dresden, Germany.

Regeneration in Hematopoiesis and Animal Models in Hematopoiesis, Institute for Immunology, Technische Universität Dresden, Fetschertrasse 74, 01307 Dresden, Germany.

出版信息

Biomaterials. 2015;53:709-15. doi: 10.1016/j.biomaterials.2015.02.095. Epub 2015 Mar 26.

Abstract

Deciphering exogenous cues that determine stem cell fate decisions is a persisting challenge of cell biology and bioengineering. In an effort to unravel the role of spatial constraints in the cell-instructive characteristics of bone marrow microenvironments, murine hematopoietic stem and progenitor cells (HSPC) were exposed to fibronectin-coated microcavities in vitro. Microcavity sizes were chosen to allow for the inclusion of either individual or multiple cells. Repopulation experiments using lethally irradiated mice showed that the maintenance of functional HSPC in culture critically depends on cavity dimensions. Short-term repopulating hematopoietic stem cells (ST-HSC) were found to be best supported within single-cell sized compartments while long-term repopulating HSC (LT-HSC) were maintained within both cavity sizes. In sum, the reported data reveal spatial restriction to be a simple but powerful means for directing HSPC fate ex vivo.

摘要

解析决定干细胞命运决定的外源性线索是细胞生物学和生物工程的一个持续挑战。为了揭示空间限制在骨髓微环境中细胞指令特征中的作用,研究人员将小鼠造血干细胞和祖细胞(HSPC)暴露于体外的纤连蛋白涂层微腔中。选择微腔的大小以允许包含单个或多个细胞。使用致死性辐照小鼠进行的再定植实验表明,功能 HSPC 在培养中维持的关键取决于腔尺寸。发现短期重定植造血干细胞(ST-HSC)在单细胞大小的隔室中得到最好的支持,而长期重定植 HSC(LT-HSC)则在两种腔室大小中都得到维持。总之,所报道的数据表明空间限制是一种简单但强大的体外指导 HSPC 命运的方法。

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