4.7 Article

Identification of Intercellular Crosstalk between Decidual Cells and Niche Cells in Mice

Journal

Publisher

MDPI
DOI: 10.3390/ijms22147696

Keywords

decidualization; mouse; single-cell RNA-seq; transcriptional changes

Funding

  1. National Natural Science Foundation of China [32070845, 31771665, 2021B1515020079]
  2. Innovation Team Project of Guangdong University [2019KCXTD001]
  3. Guangdong Special Support Program [2019BT02Y276]

Ask authors/readers for more resources

This study utilized a mouse model to generate a single-cell transcriptomic atlas of a mouse uterus during decidualization, revealing global gene expression changes in each cell type during this process. Additionally, it identified intercellular crosstalk between decidual cells and niche cells, including immune cells, endothelial cells, and trophoblast cells. The data provide a valuable resource for deciphering the molecular mechanism underlying decidualization.
Decidualization is a crucial step for human reproduction, which is a prerequisite for embryo implantation, placentation and pregnancy maintenance. Despite rapid advances over recent years, the molecular mechanism underlying decidualization remains poorly understood. Here, we used the mouse as an animal model and generated a single-cell transcriptomic atlas of a mouse uterus during decidualization. By analyzing the undecidualized inter-implantation site of the uterus as a control, we were able to identify global gene expression changes associated with decidualization in each cell type. Additionally, we identified intercellular crosstalk between decidual cells and niche cells, including immune cells, endothelial cells and trophoblast cells. Our data provide a valuable resource for deciphering the molecular mechanism underlying decidualization.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available