Transcriptome Dynamics of Hematopoietic Stem Cell Formation Revealed Using a Combinatorial Runx1 and Ly6a Reporter System

被引:9
作者
Chen, Michael J. [1 ,2 ,3 ,4 ,9 ]
da Rocha, Edroaldo Lummertz [1 ,2 ,3 ,4 ,10 ]
Cahan, Patrick [5 ]
Kubaczka, Caroline [1 ,2 ,3 ,4 ]
Hunter, Phoebe [1 ,2 ,3 ]
Sousa, Patricia [1 ,2 ,3 ]
Mullin, Nathaniel K. [1 ,2 ,3 ]
Fujiwara, Yuko [1 ,2 ]
Minh Nguyen [1 ,2 ]
Tan, Yuqi [5 ]
Zhou, Yi [1 ,2 ,3 ,4 ]
North, Trista E. [1 ,2 ,3 ,4 ,6 ]
Zon, Leonard, I [1 ,2 ,3 ,6 ,7 ,8 ]
Daley, George Q. [1 ,2 ,3 ,4 ,6 ]
Schlaeger, Thorsten M. [1 ,2 ,3 ,4 ,6 ]
机构
[1] Harvard Med Sch, Div Pediat Hematol Oncol, Boston Childrens Hosp, Boston, MA 02115 USA
[2] Harvard Med Sch, Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Harvard Med Sch, Boston Childrens Hosp, Stem Cell Program, Boston, MA 02115 USA
[4] Harvard Med Sch, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[5] Johns Hopkins Univ, Inst Cell Engn, Dept Biomed Engn, Sch Med, Baltimore, MD 21205 USA
[6] Harvard Univ, Harvard Stem Cell Inst, Boston, MA 02115 USA
[7] Harvard Univ, Howard Hughes Med Inst, Boston, MA 02115 USA
[8] Harvard Univ, Stem Cell & Regenerat Biol Dept, Boston, MA 02115 USA
[9] Acad Sinica, Inst Mol Biol, Taipei, Taiwan
[10] Univ Fed Santa Catarina, Dept Microbiol Immunol & Parasitol, Florianopolis, SC, Brazil
关键词
YOLK-SAC; ENDOTHELIAL-CELLS; PROGENITOR CELLS; IN-VIVO; MOLECULAR CHARACTERIZATION; DEFINITIVE HEMATOPOIESIS; AORTIC ENDOTHELIUM; GENE-EXPRESSION; SELF-RENEWAL; ORIGIN;
D O I
10.1016/j.stemcr.2020.03.020
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Studies of hematopoietic stem cell (HSC) development from pre-HSC-producing hemogenic endothelial cells (HECs) are hampered by the rarity of these cells and the presence of other cell types with overlapping marker expression profiles. We generated a Tg(Runx1-mKO2; Ly6a-GFP) dual reporter mouse to visualize hematopoietic commitment and study pre-HSC emergence and maturation. Runx1-mKO2 marked all intra-arterial HECs and hematopoietic cluster cells (HCCs), including pre-HSCs, myeloid- and lymphoid progenitors, and HSCs themselves. However, HSC and lymphoid potential were almost exclusively found in reporter double-positive (DP) cells. Robust HSC activity was first detected in DP cells of the placenta, reflecting the importance of this niche for (pre-)HSC maturation and expansion before the fetal liver stage. A time course analysis by single-cell RNA sequencing revealed that as pre-HSCs mature into fetal liver stage HSCs, they show signs of interferon exposure, exhibit signatures of multi-lineage differentiation gene expression, and develop a prolonged cell cycle reminiscent of quiescent adult HSCs.
引用
收藏
页码:956 / 971
页数:16
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