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Single-nucleus RNA sequencing of human trophoblast organoids and endometrial organoids co-culture model

GSE324114 Homo sapiens Expression profiling by high throughput sequencing 3 samples Submitted 2026/03/09 Platform GPL34284
Summary
To model the maternal–fetal interface, we co-cultured rotation-derived human trophoblast organoids (hTOr) with human endometrial organoids (hEMO). Here, we performed single-nucleus RNA sequencing of hEMO mono-culture, hTOr mono-culture, and their co-culture to dissect the transcriptomic landscape of this interaction. Our analysis reveals that hTOr-derived signals drive a metabolic and secretory activation in the endometrial epithelium. We identified a unique 'Activated' hEMO population emerging specifically upon co-culture, distinct from the LGR5+ homeostatic state. This transition was characterized by a robust upregulation of oxidative phosphorylation and glycolysis, concurrent with sustained proliferation, demonstrating that the trophoblast actively reprograms the endometrium into a hyper-metabolic state.
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Direct links to NCBI, no account and no request form: the whole study as GSE324114_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 3 samples. Raw sequencing reads are also available from ENA.

Also filed as BioProject PRJNA1433461 and SRA study SRP681732. Searching any of these in the dataset finder brings you back here.

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