Human trophectoderm becomes multi-layered by internalization at the polar region.

Dev Cell

Wellcome - MRC Stem Cell Institute, University of Cambridge, Jeffrey Cheah Biomedical Centre, Puddicombe Way, Cambridge CB2 0AW, UK; Department of Physiology, Development and Neuroscience, University of Cambridge, Tennis Court Road, Cambridge CB2 3EG, UK; Centre for Trophoblast Research, University of Cambridge, Cambridge, UK. Electronic address:

Published: September 2024

AI Article Synopsis

  • Mammalian embryos form blastocysts with a trophectoderm (TE) layer and an inner cell mass (ICM), which are essential for implantation, differing by species.
  • Murine embryos have a single-layered TE until they implant, while human blastocysts attach directly to the uterine wall with a unique TE structure.
  • Research shows human TE may multi-layer before implantation, crucial for securing the embryo and starting placenta formation, with most inner TE cells originating from the outer TE rather than the ICM.

Article Abstract

To implant in the uterus, mammalian embryos form blastocysts comprising trophectoderm (TE) surrounding an inner cell mass (ICM), confined to the polar region by the expanding blastocoel. The mode of implantation varies between species. Murine embryos maintain a single layered TE until they implant in the characteristic thick deciduum, whereas human blastocysts attach via polar TE directly to the uterine wall. Using immunofluorescence (IF) of rapidly isolated ICMs, blockade of RNA and protein synthesis in whole embryos, or 3D visualization of immunostained embryos, we provide evidence of multi-layering in human polar TE before implantation. This may be required for rapid uterine invasion to secure the developing human embryo and initiate formation of the placenta. Using sequential fluorescent labeling, we demonstrate that the majority of inner TE in human blastocysts arises from existing outer cells, with no evidence of conversion from the ICM in the context of the intact embryo.

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Source
http://dx.doi.org/10.1016/j.devcel.2024.05.028DOI Listing

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