AI Article Synopsis

  • The study examines the invasive trophoblast cell lineages in both rats and humans, focusing on their role in forming the uterine-placental interface in a hemochorial placenta.
  • Researchers utilized single-nucleus ATAC-seq data from rat tissues to analyze chromatin accessibility in various cell types and compare it to human trophoblast cells.
  • The results revealed similarities in gene regulation between species and identified a conserved gene regulatory network, paving the way for future studies on the regulatory mechanisms of invasive trophoblast cells.

Article Abstract

The invasive trophoblast cell lineages in rat and human share crucial responsibilities in establishing the uterine-placental interface of the hemochorial placenta. These observations have led to the rat becoming an especially useful animal model for studying hemochorial placentation. However, our understanding of similarities or differences between regulatory mechanisms governing rat and human invasive trophoblast cell populations is limited. In this study, we generated single-nucleus ATAC-seq data from gestation day 15.5 and 19.5 rat uterine-placental interface tissues, and integrated the data with single-cell RNA-seq data generated at the same stages. We determined the chromatin accessibility profiles of invasive trophoblast, natural killer, macrophage, endothelial and smooth muscle cells, and compared invasive trophoblast chromatin accessibility with extravillous trophoblast cell accessibility. In comparing chromatin accessibility profiles between species, we found similarities in patterns of gene regulation and groups of motifs enriched in accessible regions. Finally, we identified a conserved gene regulatory network in invasive trophoblast cells. Our data, findings and analysis will facilitate future studies investigating regulatory mechanisms essential for the invasive trophoblast cell lineage.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10445752PMC
http://dx.doi.org/10.1242/dev.201826DOI Listing

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