# Dynamic roles of ILC3 in endometrial repair and regeneration

**Authors:** Antonia O Cuff, Ee Von Woon, Thomas Bainton, Brendan Browne, Phoebe M Kirkwood, Frances Collins, Douglas A Gibson, Philippa T K Saunders, Andrew W Horne, Mark R Johnson, David A MacIntyre, Victoria Male

PMC · DOI: 10.1093/discim/kyaf004 · Discovery Immunology · 2025-03-26

## TL;DR

This study explores how a specific type of immune cell, ILC3, helps repair and regenerate the uterine lining during key life events like menstruation and childbirth.

## Contribution

The paper identifies two distinct subsets of ILC3 in the uterine mucosa and their dynamic roles in endometrial repair and regeneration.

## Key findings

- CD127− ILC3 are most active during menstruation and postpartum, suggesting a role in endometrial repair.
- CD127+ ILC3 are most active after menstruation, indicating a role in endometrial regeneration.
- In endometriosis, ILC3 are spatially distant from epithelial and endothelial cells, potentially impairing regeneration.

## Abstract

Innate lymphoid cells (ILCs) are prominent in the human uterine mucosa and play physiological roles in pregnancy. ILC3 are the second-most common ILC subset in the uterine mucosa, but their role remains unclear.

Here we define two subsets of lineage-negative CD56+ CD117+ CRTH2-uterine ILC3, distinguished by their expression of CD127.

The CD127− subset is most numerous and active during menstruation and immediately after parturition, suggesting a role in the repair of the uterine mucosa (called endometrium outside of pregnancy); the CD127+ subset is most numerous and active immediately after menstruation, as the endometrium regenerates. In healthy endometrium, ILC3 are spatially associated with glandular epithelial and endothelial cells, which both express receptors for the ILC3-derived cytokines, IL-22 and IL-8. In the eutopic endometrium of people with endometriosis, ILC3 are located further from glandular epithelial and endothelial cells suggesting that these cells may be less exposed to ILC3 products, potentially with negative consequences for endometrial regeneration.

Our findings highlight the dynamic nature of ILC3 in the uterine mucosa and suggest their primary role is in repair and regeneration. An improved understanding of uterine ILC3 will inform future research on endometrial health and disease.

Graphical Abstract

## Linked entities

- **Proteins:** IL22 (interleukin 22), CXCL8 (C-X-C motif chemokine ligand 8)
- **Diseases:** endometriosis (MONDO:0005133)

## Full-text entities

- **Genes:** CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL7R (interleukin 7 receptor) [NCBI Gene 3575] {aka CD127, CDW127, IL-7R-alpha, IL-7Ralpha, IL7RA, IL7Ralpha}, IL22 (interleukin 22) [NCBI Gene 50616] {aka IL-21, IL-22, IL-D110, IL-TIF, ILTIF, TIFIL-23}, NCAM1 (neural cell adhesion molecule 1) [NCBI Gene 4684] {aka CD56, MSK39, NCAM}, KIT (KIT proto-oncogene, receptor tyrosine kinase) [NCBI Gene 3815] {aka C-Kit, CD117, MASTC, PBT, SCFR}, PTGDR2 (prostaglandin D2 receptor 2) [NCBI Gene 11251] {aka CD294, CRTH2, DL1R, DP2, GPR44}
- **Diseases:** endometriosis (MESH:D004715)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12038238/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12038238/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12038238/full.md

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Source: https://tomesphere.com/paper/PMC12038238