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Modeling human embryo adhesion using a microfluidic platform
DOI:10.1126/sciadv.adz2249.png)
Abstract
En 中文
Embryo adhesion represents a critical step of implantation, yet understanding this process has been hindered by the lack of human in vitro platforms that replicate endometrial physiology. Here, we present a dual-channel microfluidic platform containing organoid-derived endometrial epithelium and primary stromal cells. Our model recapitulates important endometrial hallmarks including epithelial polarization, stromal decidualization, extracellular vesicle release, and hormone-induced receptivity. We validated the model using mouse embryos and human blastocysts, where we showed that embryos displayed features of initial adhesion. These included establishment of embryo-epithelial contacts initiated via the polar trophectoderm, inner cell mass repositioning, and lineage reorganization. Moreover, human embryos secreted βhCG indicating a functional trophoblast. Thus, this work provides a platform to study key features of embryo adhesion and endometrial receptivity and disorders affecting embryo-endometrium interactions.
Journal
IF:
12.5
Papers:
2.1W
Citations:
18.1W
Organization
Cited Papers
WebGestalt 2024: faster gene set analysis and new support for metabolomics and multi-omics
NUCLEIC ACIDS RESEARCH
IF13.1
Mapping the temporal and spatial dynamics of the human endometrium in vivo and in vitro
NATURE GENETICS
IF31.8
MAST: a flexible statistical framework for assessing transcriptional changes and characterizing heterogeneity in single-cell RNA sequencing data
GENOME BIOLOGY
IF9.4
Hsa-miR-30d, secreted by the human endometrium, is taken up by the pre-implantation embryo and might modify its transcriptome
DEVELOPMENT
IF3.6

