Cell type and region- specific transcriptional changes in the endometrium of women with RIF identify potential treatment targets

• 成果类型: Article
• 署名作者: Tempest, Nicola; Soul, Jamie; Hill, Christopher J.; Gutierrez, Eva Caamano; Hapangama, Dharani K.
• 署名单位: University of Liverpool; University of Liverpool; University of Liverpool
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-10817
• DOI: 10.1073/pnas.2421254122
• 发表日期: 2025-03-18
• 关键词: recurrent implantation failure; expression; embryo; decidualization

摘要

Recurrent implantation failure (RIF) is a devastating condition that leaves many undergoing fertility treatment childless. The human endometrium is receptive to a blastocyst for a brief period, the window of implantation. Critical knowledge underpinning biological processes leading to RIF, essential for effective treatment, is lacking. We employed spatial transcriptomics to define region- and cell- type- specific differences in endometrial gene expression in luteinizing hormone timed biopsies between women with RIF (n = 8) and fertile controls (FC) (n = 8). Differentially expressed genes (DEGs) were identified when comparing endometrial regions between FC and RIF (685 luminal epithelium, 293 glandular epithelium, 419 subluminal stroma, 264 functionalis stroma, 1,125 subluminal stromal CD45+ leukocytes, and 1,049 functionalis stromal CD56+ leukocytes). Only 57 DEGs were common to all subregions and cell types, which highlights that multiple DEGs are lost when the endometrium is examined as a single entity. When RIF- specific DEGs were leveraged against knowledge from mouse genetic models, genes associated with aberrant embryo implantation phenotypes were observed, mostly in immune cell populations. Dysregulated pathways in specific endometrial regions included the WNT signaling pathway, altered in the functionalis and subluminal stroma. Response to estradiol and ovulation cycle pathways were dysregulated in the subluminal stroma. In silico drug screening identified potential compounds that can reverse the RIF gene expression profile (e.g., raloxifene, bisoprolol). Our findings, in a well- characterized cohort, highly endorse consideration of each endometrial region and cell type as separate entities. Ignoring individual regions and composite cell populations will overlook important aberrations, forego potential treatment targets, and lead to research waste pursuing clinically irrelevant treatment options.