Understanding Hematopoietic Stem Cell Development through Functional Correlation of Their Proliferative Status with the Intra-aortic Cluster Architecture

被引:48
作者
Batsivari, Antoniana [1 ]
Rybtsov, Stanislav [1 ]
Souilhol, Celine [2 ]
Binagui-Casas, Anahi [1 ]
Hills, David [1 ]
Zhao, Suling [1 ]
Travers, Paul [1 ]
Medvinsky, Alexander [1 ]
机构
[1] Univ Edinburgh, Med Res Council Ctr Regenerat Med, Inst Stem Cell Res, SCRM Bioquarter, 5 Little France Dr, Edinburgh EH16 4UU, Midlothian, Scotland
[2] Univ Sheffield, Dept Infect Immun & Cardiovasc Dis, Sheffield S10 2RX, S Yorkshire, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
MOUSE EMBRYO AORTA; SELF-RENEWAL; AGM REGION; C-KIT; DEFINITIVE HSCS; YOLK-SAC; CYCLE; NICHE; DIFFERENTIATION; PRECURSORS;
D O I
10.1016/j.stemcr.2017.04.003
中图分类号
Q813 [细胞工程];
学科分类号
摘要
During development, hematopoietic stem cells (HSCs) emerge in the aorta-gonad-mesonephros (AGM) region through a process of multi-step maturation and expansion. While proliferation of adult HSCs is implicated in the balance between self-renewal and differentiation, very little is known about the proliferation status of nascent HSCs in the AGM region. Using Fucci reporter mice that enable in vivo visualization of cell-cycle status, we detect increased proliferation during pre-HSC expansion followed by a slowing down of cycling once cells start to acquire a definitive HSC state, similar to fetal liver HSCs. We observe time-specific changes in intra-aortic hematopoietic clusters corresponding to HSC maturation stages. The proliferative architecture of the clusters is maintained in an orderly anatomical manner with slowly cycling cells at the base and more actively proliferating cells at the more apical part of the cluster, which correlates with c-KIT expression levels, thus providing an anatomical basis for the role of SCF in HSC maturation.
引用
收藏
页码:1549 / 1562
页数:14
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