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Exposure to polystyrene microplastics during lactational period alters immune status in both male mice and their offspring

The Science of The Total Environment 2024 17 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 60 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Qian Shang, Han Wu, Han Wu, Ke Wang, Mengge Zhang, Yunde Dou, Xiaohong Jiang, Yueran Zhao, Zhao Han, Zi‐Jiang Chen, Jianfeng Wang, Yuehong Bian

Summary

This study found that when male mice were exposed to polystyrene microplastics during the nursing period, both the adult mice and their offspring showed changes in immune cell populations in the spleen. The microplastics altered the balance of different types of immune cells, suggesting the immune system was being disrupted. This is especially concerning because it shows that microplastic exposure during early life can affect immune development in the next generation.

Polymers
Body Systems
Models

The widespread use of microplastics and their harmful effects on the environment have emerged as serious concerns. However, the effect of microplastics on the immune system of mammals, particularly their offspring, has received little attention. In this study, polystyrene microplastics (PS-MPs) were orally administered to male mice during lactation. Flow cytometry was used to assess the immune cells in the spleens of both adult male mice and their offspring. The results showed that mice exposed to PS-MPs exhibited an increase in spleen weight and an elevated number of B and regulatory T cells (Tregs), irrespective of dosage. Furthermore, the F male offspring of the PS-MPs-exposed group had enlarged spleens; an increased number of B cells, T helper cells (Th cells), and Tregs; and an elevated ratio of T helper cells 17 (Th17 cells) to Tregs and T helper cells 1 (Th1 cells) to T helper cells 2 (Th2 cells). These results suggested a pro-inflammatory state in the spleen. In contrast, in the F female offspring exposed to PS-MPs, the changes in splenic immune cells were less pronounced. In the F generation of mice with exposed to PS-MPs, minimal alterations were observed in spleen immune cells and morphology. In conclusion, our study demonstrated that exposure to real human doses of PS-MPs during lactation in male mice altered the immune status, which can be passed on to F offspring but is not inherited across generations.

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