# Immunohistochemical Detection of the Mechano-Gated Piezo Channels in the Normal Endometrium and in Endometriosis

**Authors:** Angel Sánchez del Rio, Yolanda García-Mesa, Ana Gutiérrez-Palacios, Patricia Cuendias, Eliseo Viña, Graciela Martínez-Barbero, José A. Vega, Olivia García-Suárez

PMC · DOI: 10.3390/biom16010166 · Biomolecules · 2026-01-19

## TL;DR

This study uses immunohistochemistry to detect Piezo1 and Piezo2 ion channels in healthy endometrium and endometriosis, finding increased Piezo1 in ectopic lesions.

## Contribution

The first detection of Piezo1 and Piezo2 in healthy human endometrium and their altered expression in endometriosis.

## Key findings

- Piezo1 is present in glands and stroma of healthy endometrium and increased in ectopic endometriosis.
- Piezo2 is present at low levels in healthy endometrium and increases in ovarian and vaginal endometriosis.
- The findings are descriptive and suggest a potential role for Piezo channels in endometriosis pathogenesis.

## Abstract

Endometriosis is an inflammatory estrogen-dependent disorder characterized by pain, dyspareunia, dysmenorrhea, and infertility. This is due to the invasion of different organs by endometrial tissue that causes inflammation, angiogenesis, and fibrosis. The ion channels Piezo1 and Piezo2 primarily work as mechanosensors and mechanotransducers but also have functions that could participate in the clinical hallmarks of endometriosis. Thus, we investigated the occurrence and localization of Piezo1 and Piezo2 in healthy human endometrium and in endometriosis using immunohistochemistry. In healthy endometrium, Piezo1 immunoreactivity was detected in the glands and to a lesser extent in the stroma; Piezo2 was present in the same locations but at low or residual levels. In ectopic endometriosis, there was an increase in the intensity of Piezo1 regardless of location; Piezo2 only showed a net increase in the ovarian and vaginal endometriosis foci. The present results demonstrate the occurrence of Piezo ion channels in the healthy human endometrium for the first time, as well as an increase in Piezo1 in ectopic endometriosis, and no changes in Piezo2 with the exception of the ovary and vagina. However, these results are descriptive and qualitative, although they may serve as the basis for further studies. The role of these ion channels in the endometrium and in the pathogenesis of endometriosis remains to be elucidated, and more precise methods are needed to follow up on this pilot study that can be better analyzed statistically to confirm the results.

## Linked entities

- **Genes:** PIEZO1 (piezo type mechanosensitive ion channel component 1 (Er blood group)) [NCBI Gene 9780], PIEZO2 (piezo type mechanosensitive ion channel component 2) [NCBI Gene 63895]
- **Diseases:** endometriosis (MONDO:0005133)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** PIEZO1 (piezo type mechanosensitive ion channel component 1 (Er blood group)) [NCBI Gene 9780] {aka DHS, ER, FAM38A, LMPH3, LMPHM6, Mib}, PIEZO2 (piezo type mechanosensitive ion channel component 2) [NCBI Gene 63895] {aka C18orf30, C18orf58, DA3, DA5, DAIPT, FAM38B}
- **Diseases:** inflammation (MESH:D007249), pain (MESH:D010146), infertility (MESH:D007246), fibrosis (MESH:D005355), dyspareunia (MESH:D004414), dysmenorrhea (MESH:D004412), Endometriosis (MESH:D004715)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12839098/full.md

## References

59 references — full list in the complete paper: https://tomesphere.com/paper/PMC12839098/full.md

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Source: https://tomesphere.com/paper/PMC12839098