# Tamoxifen triggers a transcriptional switch from proliferation to differentiation in the circumvallate taste epithelium in mice

**Authors:** Norihito Oura, Eriko Koyanagi-Matsumura, Aya Hagimoto, Mitsuru Saito, Hideto Saijo, Hirohito Miura

PMC · DOI: 10.1038/s41598-025-32701-8 · 2025-12-17

## TL;DR

Tamoxifen causes taste cells in mice to shift from growing to maturing, which could affect taste research using this drug.

## Contribution

The study reveals tamoxifen's direct effect on taste epithelium by inducing a transcriptional shift from proliferation to differentiation.

## Key findings

- Tamoxifen reduces cell supply to taste buds in a dose-dependent manner.
- Tamoxifen downregulates cell cycle genes and upregulates differentiation-related genes in the circumvallate epithelium.
- Transcription factors like Pou2f3, Ascl1, and Nkx2-2 are induced, promoting differentiation of all taste cell types.

## Abstract

The tamoxifen-inducible Cre-loxP system is an indispensable experimental tool in life sciences for inducing spatiotemporally controlled genetic recombination in the target tissues of living animals. The use of this technology is expected to increase in taste research. However, the direct effects of tamoxifen on taste buds remain largely unexplored. Here, we demonstrate that tamoxifen reduces cell supply to the taste buds in a dose-dependent manner. RNA sequencing of the circumvallate epithelium revealed that tamoxifen induced a transcriptional shift from proliferation to differentiation. The genes regulating the cell cycle were downregulated, whereas genes promoting the differentiation of epithelial cells and keratinocytes were upregulated. Within taste buds, Shh was downregulated in immature precursor cells, whereas cell type-specific genes were broadly upregulated in mature taste bud cells. Notably, transcription factors driving taste cell type differentiation, such as Pou2f3, Ascl1, and Nkx2-2, were induced, suggesting that tamoxifen activates transcription to promote the differentiation of all cell types in taste buds, rather than activating particular signaling pathways in specific cell types. These findings indicate that tamoxifen rapidly triggers a transcriptional switch from proliferation to differentiation in the circumvallate taste epithelium, highlighting a potential confounding effect in taste research that employs tamoxifen administration.

The online version contains supplementary material available at 10.1038/s41598-025-32701-8.

## Linked entities

- **Genes:** SHH (sonic hedgehog signaling molecule) [NCBI Gene 6469], POU2F3 (POU class 2 homeobox 3) [NCBI Gene 25833], ASCL1 (achaete-scute family bHLH transcription factor 1) [NCBI Gene 429], NKX2-2 (NK2 homeobox 2) [NCBI Gene 4821]
- **Chemicals:** tamoxifen (PubChem CID 2733526)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Nkx2-2 (NK2 homeobox 2) [NCBI Gene 18088] {aka Nkx-2.2, Nkx2.2, tinman}, Ascl1 (achaete-scute family bHLH transcription factor 1) [NCBI Gene 17172] {aka ASH1, Mash1, bHLHa46}, Shh (sonic hedgehog) [NCBI Gene 20423] {aka 9530036O11Rik, Dsh, HHG-1, Hhg1, Hx, Hxl3}, Pou2f3 (POU domain, class 2, transcription factor 3) [NCBI Gene 18988] {aka Epoc-1, Oct-11a, Oct11, Otf-11, Otf11, Skin}
- **Chemicals:** Tamoxifen (MESH:D013629)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12827983/full.md

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Source: https://tomesphere.com/paper/PMC12827983