Human embryo polarization requires PLC signaling to mediate trophectoderm specification
0301 basic medicine
Time Factors
590
Phospholipase C beta
Embryo Culture Techniques
Phosphoinositide Phospholipase C
Pregnancy
cell biology
Biology (General)
pre-implantation
cell fate
0303 health sciences
Q
R
Cell Polarity
Gene Expression Regulation, Developmental
Cell Differentiation
human embryo
cell polarity
Cell polarity
Medicine
Female
Research Article
Signal Transduction
Adult
570
Cell biology
QH301-705.5
Science
GATA3 Transcription Factor
Gene Expression Regulation, Enzymologic
QH301
developmental biology
Young Adult
03 medical and health sciences
Human embryo
Humans
Cell Lineage
Preimplantation
Body Patterning
polarization
preimplantation
Cell Biology
Embryo, Mammalian
Actins
QR
Other
Developmental Biology
DOI:
10.7554/elife.65068
Publication Date:
2021-09-27T12:13:41Z
AUTHORS (21)
ABSTRACT
Apico-basal polarization of cells within the embryo is critical for segregation distinct lineages during mammalian development. Polarized become trophectoderm (TE), which forms placenta, and apolar inner cell mass (ICM), founding population fetus. The cellular molecular mechanisms leading to human its timing embryogenesis have remained unknown. Here, we show that occurs in two steps: it begins with apical enrichment F-actin followed by accumulation PAR complex. This two-step process leads formation an domain at 8-16 stage. Using RNA interference, requires Phospholipase C (PLC) signaling, specifically enzymes PLCB1 PLCE1, from eight-cell stage onwards. Finally, although expression TE differentiation marker GATA3 can be initiated independently polarization, downregulation PLCE1 decreases through a reduction number polarized cells. Therefore, reinforces fate. results present here demonstrate how triggered regulate first lineage embryos.
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CITATIONS (42)
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