| Literature DB >> 32968278 |
Claudia Gerri1, Afshan McCarthy1, Gregorio Alanis-Lobato1, Andrej Demtschenko2, Alexandre Bruneau3, Sophie Loubersac3,4, Norah M E Fogarty1,5, Daniel Hampshire6, Kay Elder7, Phil Snell7, Leila Christie7, Laurent David3,8, Hilde Van de Velde2,9, Ali A Fouladi-Nashta6, Kathy K Niakan10,11.
Abstract
Current understandings of cell specification in early mammalian pre-implantation development are based mainly on mouse studies. The first lineage differentiation event occurs at the morula stage, with outer cells initiating a trophectoderm (TE) placental progenitor program. The inner cell mass arises from inner cells during subsequent developmental stages and comprises precursor cells of the embryo proper and yolk sac1. Recent gene-expression analyses suggest that the mechanisms that regulate early lineage specification in the mouse may differ in other mammals, including human2-5 and cow6. Here we show the evolutionary conservation of a molecular cascade that initiates TE segregation in human, cow and mouse embryos. At the morula stage, outer cells acquire an apical-basal cell polarity, with expression of atypical protein kinase C (aPKC) at the contact-free domain, nuclear expression of Hippo signalling pathway effectors and restricted expression of TE-associated factors such as GATA3, which suggests initiation of a TE program. Furthermore, we demonstrate that inhibition of aPKC by small-molecule pharmacological modulation or Trim-Away protein depletion impairs TE initiation at the morula stage. Our comparative embryology analysis provides insights into early lineage specification and suggests that a similar mechanism initiates a TE program in human, cow and mouse embryos.Entities:
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Year: 2020 PMID: 32968278 PMCID: PMC7116563 DOI: 10.1038/s41586-020-2759-x
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962