共 1 条
A microfluidic platform for anterior-posterior human endoderm patterning via countervailing morphogen gradients in vitro
被引:0
|作者:
Engel, Leeya
[1
,2
]
Liu, Kevin J.
[3
]
Cui, Kiara W.
[1
]
de la Serna, Eva L.
[1
]
Vachharajani, Vipul T.
[1
,4
]
Dundes, Carolyn E.
[3
,5
]
Zheng, Sherry Li
[3
,5
]
Begur, Manali
[3
]
Loh, Kyle M.
[3
,5
]
Ang, Lay Teng
[3
,6
]
Dunn, Alexander R.
[1
]
机构:
[1] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[2] Technion Israel Inst Technol, Fac Mech Engn, IL-3200003 Haifa, Israel
[3] Stanford Univ, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
[4] Stanford Univ, Program Biophys, Med Scientist Training Program, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Dev Biol, Stanford, CA 94305 USA
[6] Stanford Univ, Dept Urol, Stanford, CA 94305 USA
来源:
基金:
美国国家卫生研究院;
关键词:
POSITIONAL INFORMATION;
MOLECULAR-WEIGHT;
NEURAL-TUBE;
STEM-CELLS;
EXPRESSION;
GENERATION;
SIGNALS;
ISL1;
D O I:
10.1016/j.isci.2025.111744
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Understanding how morphogen gradients spatially pattern tissues is a fundamental question in developmental biology but can be difficult to directly address using conventional approaches. Here, we expose hPSC-derived endoderm cells to countervailing gradients of anteriorizing and posteriorizing signals using a widely available microfluidic device. This approach yielded spatially patterned cultures comprising anterior foregut (precursor to the thyroid, esophagus, and lungs) and mid/hindgut (precursor to the intestines) cells, whose identities were confirmed using single-cell RNA sequencing (scRNA-seq). By exposing stem cells to externally applied signaling gradients, this widely accessible microfluidic platform should accelerate the production of spatially patterned tissues, complementing internally self-organizing organoids. Applying artificial morphogen gradients in vitro may also illuminate how developing tissues interpret signaling gradients in systems that are not readily accessible for in vivo studies.
引用
收藏
页数:18
相关论文