Suppr超能文献

黏附微腔中的造血干/祖细胞。

Hematopoietic stem and progenitor cells in adhesive microcavities.

机构信息

Leibniz Institute of Polymer Research, Max Bergmann Center of Biomaterials, Dresden, Germany.

出版信息

Integr Biol (Camb). 2009 Jun;1(5-6):427-34. doi: 10.1039/b903711j. Epub 2009 Apr 29.

Abstract

The homeostasis of hematopoietic stem and progenitor cells (HSC) in the bone marrow is regulated by a complex interplay of exogenous signals, including extracellular matrix (ECM) molecules, cell-cell contacts, and cytokines. To investigate the influence of spatial restriction and adhesive interactions on HSC fate decisions, we prepared a set of fibronectin-coated micrometer-sized cavities. Analysis of human CD133+ HSCs isolated after culture on these surfaces revealed that proliferation and differentiation is decreased when HSCs are supported by substrates with small microcavities. Single cell analysis of adherent cells also revealed decreased DNA synthesis and higher levels of HSC marker expression inside the smaller cavities. Increasing the cytokine concentration highlighted the tight balance of adhesion related signals and soluble cues acting on HSC fate decisions. Our results suggest that confining human HSCs in ECM-coated microcavities is a possible method to maintain these cells in a quiescent and immature state, an important advantage for several HSC applications.

摘要

骨髓中造血干细胞和祖细胞(HSC)的内稳性由外源性信号的复杂相互作用调节,包括细胞外基质(ECM)分子、细胞-细胞接触和细胞因子。为了研究空间限制和黏附相互作用对 HSC 命运决定的影响,我们制备了一组纤连蛋白包被的微米级小腔。在这些表面上培养后分析分离的人 CD133+HSC 表明,当 HSC 由具有小微腔的底物支持时,增殖和分化会减少。对黏附细胞的单细胞分析还显示,在较小的腔室内 DNA 合成减少,HSC 标记物的表达水平升高。增加细胞因子浓度突出了黏附相关信号和作用于 HSC 命运决定的可溶性线索之间的紧密平衡。我们的结果表明,将人 HSC 限制在 ECM 包被的微腔中可能是维持这些细胞处于静止和未成熟状态的一种方法,这对几种 HSC 应用是一个重要优势。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验