# The Emerging Role of Endothelial Ion Channels in the Control of Human Microcirculation

**Authors:** Francesco Moccia, Valentina Brunetti, Roberto Berra-Romani, Giovanni Villone, Gennaro Raimo, Teresa Soda, Giorgia Scarpellino, Germano Guerra

PMC · DOI: 10.3390/ijms27031421 · International Journal of Molecular Sciences · 2026-01-30

## TL;DR

This review explores how ion channels in human blood vessel linings control blood flow and pressure, with potential implications for treating diseases linked to vascular issues.

## Contribution

The paper reviews the specific roles of various endothelial ion channels in human microcirculation, highlighting their therapeutic potential.

## Key findings

- Endothelial ion channels like K+ and TRP regulate blood flow in human microvascular beds such as skin and brain.
- Different vascular regions use distinct ion channel repertoires for endothelium-dependent relaxation.
- Understanding these channels may lead to new treatments for cardiovascular and neurodegenerative diseases.

## Abstract

Endothelial ion signaling is crucial for the proper function of the arterial microcirculation, regulating local blood flow to meet metabolic demands and contributing to the regulation of systemic arterial pressure. The role of endothelial ion channels in the precise control of vascular resistance has been primarily investigated in animal models, where the microvasculature is more readily accessible. This review aims to discuss current knowledge on the role of endothelial ion signaling in vasomotor regulation in the human microcirculation, focusing on potassium (K+) channels (KIR2.1, KATP, SKCa/IKCa), Transient Receptor Potential (TRP) channels, particularly TRP Vanilloid 1 (TRPV1) and TRPV4, and Piezo1 channels. The analysis examines the organization of the endothelial ionic signaling machinery in the most extensively studied human microvascular beds, such as the skin, skeletal muscle, and brain, while also discussing vascular reactivity in vessels isolated ex vivo. Accumulating evidence indicates that a distinct repertoire of endothelial ion channels engages diverse endothelium-dependent vasorelaxant pathways across different vascular beds. Understanding how endothelial channels regulate the microvascular unit is predicted to foster the search for alternative therapeutic strategies for treating cardiovascular and neurodegenerative disorders associated with endothelial dysfunction.

## Linked entities

- **Genes:** KCNJ2 (potassium inwardly rectifying channel subfamily J member 2) [NCBI Gene 3759], TRPV1 (transient receptor potential cation channel subfamily V member 1) [NCBI Gene 7442], TRPV4 (transient receptor potential cation channel subfamily V member 4) [NCBI Gene 59341], PIEZO1 (piezo type mechanosensitive ion channel component 1 (Er blood group)) [NCBI Gene 9780]

## Full-text entities

- **Genes:** TRPV1 (transient receptor potential cation channel subfamily V member 1) [NCBI Gene 7442] {aka VR1}, PIEZO1 (piezo type mechanosensitive ion channel component 1 (Er blood group)) [NCBI Gene 9780] {aka DHS, ER, FAM38A, LMPH3, LMPHM6, Mib}, KCNJ2 (potassium inwardly rectifying channel subfamily J member 2) [NCBI Gene 3759] {aka ATFB9, HHBIRK1, HHIRK1, IRK1, KIR2.1, LQT7}, TRPV4 (transient receptor potential cation channel subfamily V member 4) [NCBI Gene 59341] {aka BCYM3, CMT2C, HMSN2C, OTRPC4, SMAL, SPSMA}
- **Diseases:** cardiovascular and neurodegenerative disorders (MESH:D019636), endothelial dysfunction (MESH:D014652)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

376 references — full list in the complete paper: https://tomesphere.com/paper/PMC12898815/full.md

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Source: https://tomesphere.com/paper/PMC12898815