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Engineering the hematopoietic stem cell niche: Frontiers in biomaterial science

机译:工程造血干细胞生态位:生物材料科学领域的前沿

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摘要

Hematopoietic stem cells (HSCs) play a crucial role in the generation of the body’s blood and immune cells. This process takes place primarily in the bone marrow in specialized ‘niche’ microenvironments, which provide signals responsible for maintaining a balance between HSC quiescence, self-renewal, and lineage specification required for life-long hematopoiesis. While our understanding of these signaling mechanisms continues to improve, our ability to engineer them in vitro for the expansion of clinically relevant HSC populations is still lacking. In this review, we focus on development of biomaterials-based culture platforms for in vitro study of interactions between HSCs and their local microenvironment. The tools and techniques used for both examining HSC-niche interactions as well as applying these findings towards controlled HSC expansion or directed differentiation in 2D and 3D platforms are discussed. These novel techniques hold the potential to push the existing boundaries of HSC cultures towards high-throughput, real-time, and single-cell level biomimetic approaches that enable a more nuanced understanding of HSC regulation and function. Their application in conjunction with innovative biomaterial platforms can pave the way for engineering artificial bone marrow niches for clinical applications as well as elucidating the pathology of blood-related cancers and disorders.
机译:造血干细胞(HSC)在人体血液和免疫细胞的产生中起着至关重要的作用。该过程主要发生在专门的“小生境”微环境中的骨髓中,该环境提供了维持终生造血所需的HSC静态,自我更新和血统规范之间平衡的信号。尽管我们对这些信号传导机制的理解不断提高,但我们仍缺乏在体外对其进行工程改造以扩展临床相关HSC群体的能力。在这篇综述中,我们专注于基于生物材料的培养平台的开发,用于体外研究HSC及其局部微环境之间的相互作用。讨论了用于检查HSC-利基相互作用以及将这些发现应用于2D和3D平台中受控的HSC扩展或定向分化的工具和技术。这些新颖的技术具有将HSC文化的现有边界推向高通量,实时和单细胞水平仿生方法的潜力,这些方法使人们对HSC调控和功能有了更细致的了解。将其与创新的生物材料平台结合使用可为工程化人造骨髓壁ches的临床应用铺平道路,并阐明与血液有关的癌症和疾病的病理学。

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