# Transcriptomic analysis of the TRP gene family in human brain physiopathology

**Authors:** Barbara Olejniczak, Arpita Balakrishnan, Justyna Augustyniak, Elżbieta Salińska, Agnieszka Bronisz, Jakub Godlewski

PMC · DOI: 10.3389/fnmol.2025.1576941 · Frontiers in Molecular Neuroscience · 2025-04-24

## TL;DR

This paper explores how TRP genes are expressed in the human brain and their role in brain development and disease.

## Contribution

The study provides a detailed transcriptomic analysis of TRP gene expression in the brain, linking it to neurodevelopment and disease.

## Key findings

- TRP gene expression is spatially distinct, with enrichment in the hippocampus during brain development.
- TRP genes are associated with the pathophysiology of neural tissue and conditions like aging and dementia.
- The findings suggest TRP channels could be therapeutic targets for neurodegenerative disorders.

## Abstract

The transient receptor potential (TRP) gene family is vital to cellular physiology, mediating ion flow across membranes and facilitating sensory signal transduction. This article examines the transcriptomic landscape of TRP genes, emphasizing their varying expression across organs, tissues, and cells, with a particular focus on the brain. Analysis reveals a distinct spatial distribution of TRP gene expression, notably enriched in the hippocampus during brain development, highlighting their essential role in neuronal function. Utilizing datasets from the Human Protein Atlas, Allen Human Brain Atlas, and studies on aging and dementia, associations are identified between TRP gene expression and the development or pathophysiology of neural tissue, highlighting the therapeutic potential of TRP channels in addressing, e.g., sensory impairments and cognitive decline. These insights into the regulatory dynamics of TRP channels lay a foundation for developing targeted interventions for neurodegenerative disorders.

## Linked entities

- **Genes:** TYRP1 (tyrosinase related protein 1) [NCBI Gene 7306]
- **Diseases:** dementia (MONDO:0001627)

## Full-text entities

- **Diseases:** sensory impairments (MESH:D012678), cognitive decline (MESH:D003072), dementia (MESH:D003704), neurodegenerative disorders (MESH:D019636)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12058757/full.md

## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC12058757/full.md

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Source: https://tomesphere.com/paper/PMC12058757