# The reproductive toxicity of aggregation-induced emission nanoparticles on mouse ovarian function

**Authors:** Yibin Zhang, Nan Qiao, Yihang Jiang, Miaozhuang Fan, Wenguang Zhang, Yue Jiao, Zhengzheng Li, Gang Feng, Wing-Cheung Law, Zhourui Xu, Gaixia Xu

PMC · DOI: 10.1016/j.isci.2025.114312 · 2025-12-02

## TL;DR

This study shows that certain nanoparticles used in biomedical applications can harm mouse ovarian function and reduce fertility.

## Contribution

The paper reveals how aggregation-induced emission nanoparticles affect oocyte maturation and ovarian hormone expression in mice.

## Key findings

- TPA-BT nanoparticles reduced oocyte maturation in a concentration-dependent manner.
- High concentrations of TPA-BT nanoparticles caused ovarian cell apoptosis and disrupted hormone secretion.
- The nanoparticles suppressed estrogen receptor expression in mice.

## Abstract

Luminogens with aggregation-induced emission (AIEgens) have attracted increasing attention for biomedical applications, prompting concerns regarding their potential toxicity. Although some studies have reported the in vivo toxicity of AIEgens, their reproductive effects remain insufficiently characterized. In this study, we investigated the reproductive toxicity of a representative AIEgen, TPA-BT, encapsulated into nanoparticles (NPs), with a particular focus on ovarian function in mice. Oocyte maturation rates in vitro, body weight, and organ coefficients were evaluated following TPA-BT NPs exposure. Furthermore, oocyte apoptosis and serum hormone levels were examined. TPA-BT NPs significantly reduced oocyte maturation in a concentration-dependent manner. In vivo, high concentrations induced ovarian cell apoptosis, suppressed estrogen receptor (ERα and ERβ) expression, and disrupted anti-Müllerian hormone secretion, ultimately impairing reproductive function. These findings provide critical insights into the reproductive toxicity of AIEgens and establish a foundation for further mechanistic investigations to ensure their safe application in the biomedical field.

•The reproductive toxicity of AIEgens on mouse ovarian function was studied•The study revealed that AIE NPs indirectly impact oocyte maturation via cumulus cells•High TPA-BT NPs levels disrupt hormone expression and trigger ovarian cell apoptosis

The reproductive toxicity of AIEgens on mouse ovarian function was studied

The study revealed that AIE NPs indirectly impact oocyte maturation via cumulus cells

High TPA-BT NPs levels disrupt hormone expression and trigger ovarian cell apoptosis

Biological sciences; Nanoparticles; Optical imaging; Toxicology

## Linked entities

- **Genes:** ESR1 (estrogen receptor 1) [NCBI Gene 2099], ESR2 (estrogen receptor 2) [NCBI Gene 2100]
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Esr2 (estrogen receptor 2 (beta)) [NCBI Gene 13983] {aka ER[b], ERbeta, Estrb}, Esr1 (estrogen receptor 1 (alpha)) [NCBI Gene 13982] {aka ER, ER-alpha, ERa, ERalpha, ESR, Estr}
- **Diseases:** reproductive (MESH:D060737), toxicity (MESH:D064420)
- **Chemicals:** AIEgen (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12765180/full.md

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Source: https://tomesphere.com/paper/PMC12765180