Engineering the hematopoietic stem cell niche: Frontiers in biomaterial science

被引:72
作者
Choi, Ji Sun [1 ]
Mahadik, Bhushan P. [1 ]
Harley, Brendan A. C. [1 ,2 ]
机构
[1] Univ Illinois, Dept Chem & Biomol Engn, Urbana, IL 61801 USA
[2] Univ Illinois, Carl R Woese Inst Genom Biol, Urbana, IL 61801 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Biomimetics; Hematopoietic stem cells; Hydrogel and scaffold fabrication; Stem cell fate; Stem cell niche engineering; HUMAN BONE-MARROW; HUMAN CORD BLOOD; 3-DIMENSIONAL PERFUSION CULTURE; MESENCHYMAL STROMAL CELLS; EXPANSION IN-VITRO; EX-VIVO CULTURE; PROGENITOR CELLS; REPOPULATING CELLS; ENDOTHELIAL-CELLS; CD34(+) CELLS;
D O I
10.1002/biot.201400758
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
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.
引用
收藏
页码:1529 / 1545
页数:17
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