# Modulation of Mast Cell Activation via MRGPRX2 by Natural Oat Extract

**Authors:** Susanne Kaesler, Désirée Argiriu, Shyami M. Kandage, Karla Schönfeldt, Shalva Lekiashvili, Ceren N. Dengiz, Neslim Ercan, Caterina Iuliano, Martina Herrmann, Maria Reichenbach, Dominik Cichowski, Magda Babina, Miriam Hils, Martin Köberle, Tilo Biedermann

PMC · DOI: 10.3390/ijms27010334 · International Journal of Molecular Sciences · 2025-12-28

## TL;DR

This study shows that oat extract can reduce mast cell activation through MRGPRX2, offering a natural way to manage inflammation and itching.

## Contribution

The first demonstration that oat extract inhibits MRGPRX2-mediated mast cell activation.

## Key findings

- Oat extract significantly reduced mast cell degranulation triggered by MRGPRX2 ligands.
- The inhibitory effect was confirmed using both LAD2 cells and primary human mast cells.
- Oat extract modulated MRGPRX2 signaling without affecting cell viability.

## Abstract

The Mas-related G protein-coupled receptor (MRGPR) X2 is expressed on skin mast cells and can be stimulated by an unusually broad spectrum of ligands, including specific drugs and even endogenous peptides. MRGPRX2 activation can induce mast cell degranulation and consequently mediator release, leading to inflammatory and hypersensitivity reactions. In addition, MRGPRX2 mediates pain and itching sensations, leading to increased efforts to identify MRGPRX2 inhibitors, including plant-derived compounds. Components within oat extracts have been shown to mediate anti-inflammatory and itch-relieving properties, but a possible inhibitory effect on MRGPRX2 activation has not yet been investigated. We aimed to fill this gap and explored whether an oat kernel extract can modulate MRGPRX2 activation. For this purpose, we established a mast cell model with the human LAD2 cell line and used it to investigate the consequences of exposure to oat extract. While we did not observe any influence on cell viability, we analyzed the impact of oat extract on MRGPRX2-mediated mast cell activation and degranulation initiated by the three confirmed MRGPRX2 ligands c48/80, substance P, and cortistatin 14. Exposure to oat extract resulted in a significant reduction in mast cell degranulation for all three ligands, as assessed by the release of β-hexosaminidase, tryptase, cell surface expression of CD63 and CD107a, and phosphorylation of ERK. All results were confirmed with primary human mast cells. Thus, we demonstrated for the first time that oat extract leads to a significant reduction in MRGPRX2 activation, pointing to a previously unrecognized capacity of natural compounds to modulate this pathway.

## Linked entities

- **Genes:** MRGPRX2 (MAS related GPR family member X2) [NCBI Gene 117194]
- **Proteins:** TPSB2 (tryptase beta 2), CD63 (CD63 molecule), LAMP1 (lysosome associated membrane protein 1), EPHB2 (EPH receptor B2)
- **Chemicals:** c48/80 (PubChem CID 104735), substance P (PubChem CID 36511), cortistatin 14 (PubChem CID 16133803)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** OGA (O-GlcNAcase) [NCBI Gene 10724] {aka MEA5, MGEA5, NCOAT}, CD63 (CD63 molecule) [NCBI Gene 967] {aka AD1, HOP-26, ME491, MLA1, OMA81H, Pltgp40}, MRGPRX2 (MAS related GPR family member X2) [NCBI Gene 117194] {aka MGRG3, MRGX2}, LAMP1 (lysosome associated membrane protein 1) [NCBI Gene 3916] {aka CD107a, LAMPA, LGP120}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}
- **Diseases:** hypersensitivity (MESH:D004342), pain (MESH:D010146), itch (MESH:D011537), inflammatory (MESH:D007249)
- **Chemicals:** Oat Extract (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12786182/full.md

## References

75 references — full list in the complete paper: https://tomesphere.com/paper/PMC12786182/full.md

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Source: https://tomesphere.com/paper/PMC12786182