# Nerve Growth Factor Modulates Regulatory Cell Volume Behavior via Stimulating TRPV1, TRPM8 Channels and Inducing Ca2+ Signaling in Human Conjunctival Epithelial Cells

**Authors:** Friedrich Wolf, Tina Dietrich-Ntoukas, Peter S. Reinach, Uwe Pleyer, Stefan Mergler

PMC · DOI: 10.3390/cells14100719 · Cells · 2025-05-15

## TL;DR

This study shows how nerve growth factor affects cell volume in eye cells by interacting with TRPV1 and TRPM8 channels.

## Contribution

The paper reveals opposing effects of TRPV1 and TRPM8 activation on cell volume regulation in human conjunctival epithelial cells.

## Key findings

- NGF induces intracellular Ca2+ regulation via TRPV1 and TRPM8 channels in conjunctival epithelial cells.
- TRPV1 and TRPM8 activation leads to opposing effects on cell volume responses to anisosmotic challenges.
- AMG 9810 and AMTB modulate NGF-induced cell volume changes through TRPV1 and TRPM8 pathways.

## Abstract

NGF plays important roles in ocular surface homeostasis and different pathological conditions. One effect includes promoting conjunctival epithelial cell differentiation and mucin secretion. This study characterizes the individual roles of TRPV1 and TRPM8 channel activity in mediating the effects of NGF on intracellular Ca2+ regulation and its alteration of regulatory cell volume responses to anisosmotic challenges in human conjunctival epithelial cells (IOBA-NHC). With fura-2/AM-loaded cells, the effects of 40 µM capsaicin and 20 µM AMG 9810 on Ca2+ regulation confirm functional TRPV1 expression. TRPM8 expression is evident since 500 µM menthol and 20 µM AMTB have opposing effects on [Ca2+]i. AMG 9810 and AMTB (both 20 µM) suppress the responses to NGF (100 ng/mL). With calcein/AM-loaded cells, the effects of these mediators are evaluated on apparent cell volume responses induced by an anisosmotic challenge. NGF decreases the apparent cell volume that AMG 9810 suppresses, whereas AMTB (both 20 µM) augments this response. Therefore, NGF interacts with TRPV1 and TRPM8 to induce opposing effects on cell volume regulatory behavior. These opposing effects suggest that the signaling pathways and effectors that mediate responses to TRPV1 and TRPM8 activation are not the same.

## Linked entities

- **Proteins:** TRPV1 (transient receptor potential cation channel subfamily V member 1), TRPM8 (transient receptor potential cation channel subfamily M member 8)
- **Chemicals:** NGF (PubChem CID 60160600), capsaicin (PubChem CID 1548943), AMG 9810 (PubChem CID 680502), menthol (PubChem CID 1254), AMTB (PubChem CID 16095383), calcein/AM (PubChem CID 390986), fura-2/AM (PubChem CID 105091)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** NGF (nerve growth factor) [NCBI Gene 4803] {aka Beta-NGF, HSAN5, NGFB}, TRPM8 (transient receptor potential cation channel subfamily M member 8) [NCBI Gene 79054] {aka LTRPC6, LTrpC-6, TRPP8, trp-p8}, TRPV1 (transient receptor potential cation channel subfamily V member 1) [NCBI Gene 7442] {aka VR1}, mucin [NCBI Gene 100508689]
- **Chemicals:** fura-2 (MESH:D016257), AM (MESH:D000576), Ca (MESH:D002118), AMTB (MESH:C080838), AMG 9810 (MESH:C500530), calcein (MESH:C007740)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** IOBA-NHC — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_9Y68)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12109909/full.md

## References

124 references — full list in the complete paper: https://tomesphere.com/paper/PMC12109909/full.md

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Source: https://tomesphere.com/paper/PMC12109909