The dynamics of morphogenesis in stem cell-based embryology: Novel insights for symmetry breaking

被引:9
|
作者
Sozen, Berna [1 ,2 ]
Cornwall-Scoones, Jake [1 ,3 ]
Zernicka-Goetz, Magdalena [1 ,4 ]
机构
[1] CALTECH, Div Biol & Biol Engn, 1200 E Calif Blvd, Pasadena, CA 91125 USA
[2] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA
[3] Francis Crick Inst, Dev Dynam Lab, London NW1 1AT, England
[4] Univ Cambridge, Dept Physiol Dev & Neurosci, Mammalian Embryo & Stem Cell Grp, Cambridge CB2 3EG, England
关键词
Stem cells; Embryogenesis; Symmetry breaking; Gastrulation; Signaling; In vitro; VISCERAL ENDODERM; MOUSE EMBRYO; LINEAGE ALLOCATION; NODAL ANTAGONISTS; PRIMITIVE STREAK; SIZE REGULATION; ANTERIOR; GASTRULATION; ORGANIZATION; POLARITY;
D O I
10.1016/j.ydbio.2020.12.005
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Breaking embryonic symmetry is an essential prerequisite to shape the initially symmetric embryo into a highly organized body plan that serves as the blueprint of the adult organism. This critical process is driven by morphogen signaling gradients that instruct anteroposterior axis specification. Despite its fundamental importance, what triggers symmetry breaking and how the signaling gradients are established in time and space in the mammalian embryo remain largely unknown. Stem cell-based in vitro models of embryogenesis offer an unprecedented opportunity to quantitatively dissect the multiple physical and molecular processes that shape the mammalian embryo. Here we review biochemical mechanisms governing early mammalian patterning in vivo and highlight recent advances to recreate this in vitro using stem cells. We discuss how the novel insights from these model systems extend previously proposed concepts to illuminate the extent to which embryonic cells have the intrinsic capability to generate specific, reproducible patterns during embryogenesis.
引用
收藏
页码:82 / 90
页数:9
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