Integrated single-cell and metabolomic profiling identifies ovarian metabolic differences and endothelial heterogeneity associated with litter-size variation in Hu sheep.

BACKGROUND

Hu sheep are highly prolific, but litter size remains variable among individuals. How ovarian metabolism and somatic-cell heterogeneity are associated with this variation remains unclear. Ovarian metabolites from high-litter-size (HLS) and low-litter-size (LLS) Hu ewes were profiled by liquid chromatography-mass spectrometry and gas chromatography-mass spectrometry. Ovarian cell populations and transcriptional states were characterized by single-cell RNA sequencing. Integrated analyses were used to relate metabolic differences to specific cell populations and predicted cell-cell communication. RT-qPCR and multiplex immunofluorescence were used to examine selected metabolic genes and the endothelial localization of ESM1. Separate cell experiments assessed the effects of endothelial cell-conditioned medium (EC-CM) and recombinant human IGFBP3 on primary ovine granulosa cells (GCs), with TMEM219 knockdown used to evaluate receptor involvement.

RESULTS

HLS ovaries showed higher L-carnitine abundance, whereas several representative sphingomyelin species were more abundant in LLS ovaries (nominal P < 0.05). Integrated analysis identified two EC associated genes: DNAJB4 was downregulated, whereas NDRG1 was upregulated in HLS ovaries (P < 0.05). At the EC level, gene set enrichment analysis showed significant enrichment of glutathione metabolism and oxidative phosphorylation in the HLS group. EC subclustering further associated these transcriptional programs with ESM1⁺ angiogenic endothelial cells (A-ECs). Multiplex immunofluorescence localized ESM1 to VWF-positive vascular structures and showed a significantly larger ESM1-positive area and more VWF/ESM1 double-positive cells in HLS ovaries (P < 0.05). Cell-cell communication analysis identified IGFBP3-TMEM219 as a candidate EC-GC interaction. IGFBP3 was detected in EC-conditioned medium, which significantly reduced EdU incorporation and the expression of CYP11A1, FSHR and STAR (P < 0.05) in granulosa cells. Recombinant IGFBP3 produced similar responses, and TMEM219 knockdown partially attenuated several of these effects.

CONCLUSIONS

This study identified an association between exploratory ovarian metabolic patterns and EC heterogeneity, while functional experiments showed that EC-derived IGFBP3 affected GC function partly through TMEM219. These findings suggest that endothelial state and signaling may be relevant to follicular development, although whether IGFBP3-TMEM219 signaling contributes to litter-size variation in Hu sheep remains to be established.