Departments of Surgery and of Biomedicine, Basel University Hospital, Basel, Switzerland.
Biomaterials. 2011 Jan;32(2):321-9. doi: 10.1016/j.biomaterials.2010.09.041. Epub 2010 Oct 16.
In the bone marrow, specialized microenvironments, called niches, regulate hematopoietic stem cell (HSC) maintenance and function through a complex crosstalk between different cell types. Although in vivo studies have been instrumental to elucidate some of the mechanisms by which niches exert their function, the establishment of an in vitro model that recapitulates the fundamental interactions of the niche components in a controlled setting would be of great benefit. We have previously shown that freshly harvested bone marrow- or adipose tissue-derived cells can be cultured under perfusion within porous scaffolds, allowing the formation of an organized 3D stromal tissue, composed by mesenchymal and endothelial progenitors and able to support hematopoiesis. Here we describe 3D scaffold-based perfusion systems as potential models to reconstruct ex vivo the bone marrow stem cell niche. We discuss how several culture parameters, including scaffold properties, cellular makeup and molecular signals, can be varied and controlled to investigate the role of specific cues in affecting HSC fate. We then provide a perspective of how the system could be exploited to improve stem cell-based therapies and how the model can be extended toward the engineering of other specialized stromal niches.
在骨髓中,称为龛的专门微环境通过不同细胞类型之间的复杂串扰来调节造血干细胞 (HSC) 的维持和功能。尽管体内研究对于阐明龛如何发挥其功能的一些机制非常重要,但建立一个能够在受控环境中再现龛成分基本相互作用的体外模型将非常有益。我们之前已经表明,新鲜收获的骨髓或脂肪组织来源的细胞可以在多孔支架内进行灌注培养,从而形成由间充质和内皮祖细胞组成的有组织的 3D 基质组织,并能够支持造血。在这里,我们描述了基于 3D 支架的灌注系统,作为体外重建骨髓干细胞龛的潜在模型。我们讨论了如何改变和控制几个培养参数,包括支架特性、细胞组成和分子信号,以研究特定线索在影响 HSC 命运中的作用。然后,我们提供了一个如何利用该系统来改进基于干细胞的治疗的视角,以及如何将该模型扩展到其他专门的基质龛的工程。