Notch activation during early mesoderm induction modulates emergence of the T/NK cell lineage from human iPSCs

被引:3
作者
Heinze, Dar [1 ,2 ,4 ]
Park, Seonmi [1 ,2 ]
McCracken, Andrew [1 ,2 ]
Haratianfar, Mona [1 ,2 ]
Lindstrom, Jonathan [1 ,2 ]
Villacorta-Martin, Carlos [1 ,2 ]
Mithal, Aditya [1 ,2 ]
Wang, Feiya [1 ,2 ]
Yang, Meng Wei [1 ,2 ]
Murphy, George [1 ,2 ]
Mostoslavsky, Gustavo [1 ,2 ,3 ]
机构
[1] Boston Univ, Ctr Regenerat Med, Boston, MA 02215 USA
[2] Boston Med Ctr, Boston, MA 02118 USA
[3] Boston Univ, Dept Med, Sect Gastroenterol, Boston, MA 02215 USA
[4] Boston Univ, Dept Surg, Med Ctr, Boston, MA USA
来源
STEM CELL REPORTS | 2022年 / 17卷 / 12期
关键词
antigen receptors; safety features (e; g; inducible death; STEM-CELLS; B-CELL; GENE; DIFFERENTIATION; ENDOTHELIUM; REQUIREMENT; EXPRESSION; GENERATION;
D O I
10.1016/j.stemcr.2022.10.007
中图分类号
Q813 [细胞工程];
学科分类号
摘要
A robust method of producing mature T cells from iPSCs is needed to realize their therapeutic potential. NOTCH1 is known to be required for the production of hematopoietic progenitor cells with T cell potential in vivo. Here we identify a critical window during mesodermal differentiation when Notch activation robustly improves access to definitive hematopoietic progenitors with T/NK cell lineage potential. Low-density progenitors on either OP9-hDLL4 feeder cells or hDLL4-coated plates favored T cell maturation into TCRab+CD3+CD8+ cells that express expected T cell markers, upregulate activation markers, and proliferate in response to T cell stimulus. Single-cell RNAseq shows Notch activation yields a 6-fold increase in multi-potent hematopoietic progenitors that follow a developmental trajectory toward T cells with clear similarity to post-natal human thymocytes. We conclude that early mesodermal Notch activation during hematopoietic differentiation is a missing stimulus with broad implications for producing hematopoietic progenitors with definitive characteristics.
引用
收藏
页码:2610 / 2628
页数:19
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