# UVA Light Triggers Activation of TRPV1 and TRPA1 by Staurosporine and Midostaurin

**Authors:** Sebastian Pantke, Lucas H. K. Weber, Frank G. Echtermeyer, Christine Herzog, Mirjam J. Eberhardt, Andreas Leffler

PMC · DOI: 10.3390/ijms27010227 · International Journal of Molecular Sciences · 2025-12-25

## TL;DR

This study shows that UVA light can activate TRPV1 and TRPA1 channels when combined with the drugs staurosporine and midostaurin.

## Contribution

The study identifies staurosporine and midostaurin as UVA light-dependent photosensitizers for TRPV1 and TRPA1.

## Key findings

- Staurosporine activates TRPV1 and TRPA1 only when combined with UVA light.
- Midostaurin activates TRPV1 and TRPA1 both with and without UVA light, but the effect is stronger with UVA.
- The effects of both drugs are reversed by the reducing agent dithiothreitol (DTT).

## Abstract

The activation of TRPV1 and TRPA1 by UVA light is a complex process involving channel modulation by reactive oxygen species (ROS). The present study describes staurosporine and midostaurin, two protein kinase inhibitors, as photosensitizers that can modulate the activity of TRPV1 and TRPA1 in a UVA light-dependent manner. Patch-clamp and calcium imaging were used to investigate effects of staurosporine and midostaurin on recombinant human (h) TRPV1 and TRPA1 in HEK 293T cells and on native mouse dorsal root ganglion (DRG) cells. Staurosporine applied alone did not induce channel activation, but co-application with UVA light activated both TRPV1 and TRPA1. Staurosporine with UVA light also potentiated TRPV1-mediated membrane currents induced by heat and protons. Midostaurin induced the UVA light-independent activation and sensitization of TRPV1 and TRPA1, and this effect was strongly potentiated by UVA light. Effects induced by both staurosporine and midostaurin were reversed by the reducing agent dithiothreitol (DTT). Midostaurin induced a calcium influx in TRPA1-expressing DRG neurons. Our results show that staurosporine and midostaurin modulate the activity of TRPV1 and TRPA1 channels in the presence of UVA light. These photosensitizing properties can be relevant when staurosporine is used for in vitro experiments, and they may account for the phototoxic side effects of midostaurin.

## Linked entities

- **Proteins:** TRPV1 (transient receptor potential cation channel subfamily V member 1), TRPA1 (transient receptor potential cation channel subfamily A member 1)
- **Chemicals:** staurosporine (PubChem CID 5279), midostaurin (PubChem CID 9829523), dithiothreitol (PubChem CID 19001)
- **Species:** Mus musculus (taxon 10090), Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** TRPV1 (transient receptor potential cation channel subfamily V member 1) [NCBI Gene 7442] {aka VR1}, TRPA1 (transient receptor potential cation channel subfamily A member 1) [NCBI Gene 8989] {aka ANKTM1, FEPS, FEPS1, p120}
- **Diseases:** phototoxic (MESH:D017484)
- **Chemicals:** Staurosporine (MESH:D019311), calcium (MESH:D002118), ROS (MESH:D017382), Midostaurin (MESH:C059539), DTT (MESH:D004229), UVA (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12786046/full.md

## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC12786046/full.md

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Source: https://tomesphere.com/paper/PMC12786046