Fetal liver: an ideal niche for hematopoietic stem cell expansion

被引:22
作者
Gao, Suwei [1 ]
Liu, Feng [2 ,3 ]
机构
[1] Hebei Univ, Coll Life Sci, Baoding 071002, Peoples R China
[2] Chinese Acad Sci, Inst Zool, State Key Lab Membrane Biol, Beijing 100101, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
fetal liver; niche; hematopoietic stem cell expansion; signaling network; RECEPTOR TYROSINE KINASE; C-KIT; MOUSE EMBRYO; BONE-MARROW; AORTIC ENDOTHELIUM; ERYTHROID PROGENITORS; LONG-TERM; EXPRESSION; MATURATION; BLOOD;
D O I
10.1007/s11427-018-9313-4
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Fetal liver (FL) is an intricate and highly vascularized hematopoietic organ, which can support the extensive expansion of hematopoietic stem cells (HSCs) without loss of stemness, as well as of the downstream lineages of HSCs. This powerful function of FL largely benefits from the niche (or microenvironment), which provides a residence for HSC expansion. Numerous studies have demonstrated that the FL niche consists of heterogeneous cell populations that associate with HSCs spatially and regulate HSCs functionally. At the molecular level, a complex of cell extrinsic and intrinsic signaling network within the FL niche cells maintains HSC expansion. Here, we summarize recent studies on the analysis of the FL HSCs and their niche, and specifically on the molecular regulatory network for HSC expansion. Based on these studies, we hypothesize a strategy to obtain a large number of functional HSCs via 3D reconstruction of FL organoid ex vivo for clinical treatment in the future.
引用
收藏
页码:885 / 892
页数:8
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