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
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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