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<p>Microplastics are a widespread environmental hazard and their impact on human health has become a growing concern in last years. Recently, the potential role of microplastics in the development of various diseases, including diabetes, has been highlighted. Therefore, the aim of this study was to investigate the effects of PET microplastics on the pancreas using immature pigs as a model organism. We analyzed the global transcriptomic profile of the pancreas by RNA-Seq in piglets treated with either a low (0.1&#xa0;g/day) or a high dose (1&#xa0;g/day) of PET microplastics for 4&#xa0;weeks. The analysis revealed a dose-dependent effect of PET microplastics on gene expression. A low dose changed the expression of one gene, while a high dose affected the expression of 86 genes. The differentially expressed genes, including immune cell markers, cytokines and chemokines, may activate the immune system in the pancreas in a way that is characteristic of the pathogenesis of diabetes. In addition, PET microplastics induced oxidative stress in the pancreas. These above imply that oral exposure to PET microplastics could be a new risk factor for the development of diabetes.</p>

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Oral exposure to PET microplastics induces the pancreatic immune response and oxidative stress in immature pigs

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年7月1日

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  • Karol Mierzejewski,
  • Aleksandra Kurzyńska,
  • Monika Golubska,
  • Ismena Gałęcka,
  • Jarosław Całka,
  • Iwona Bogacka

摘要

Microplastics are a widespread environmental hazard and their impact on human health has become a growing concern in last years. Recently, the potential role of microplastics in the development of various diseases, including diabetes, has been highlighted. Therefore, the aim of this study was to investigate the effects of PET microplastics on the pancreas using immature pigs as a model organism. We analyzed the global transcriptomic profile of the pancreas by RNA-Seq in piglets treated with either a low (0.1 g/day) or a high dose (1 g/day) of PET microplastics for 4 weeks. The analysis revealed a dose-dependent effect of PET microplastics on gene expression. A low dose changed the expression of one gene, while a high dose affected the expression of 86 genes. The differentially expressed genes, including immune cell markers, cytokines and chemokines, may activate the immune system in the pancreas in a way that is characteristic of the pathogenesis of diabetes. In addition, PET microplastics induced oxidative stress in the pancreas. These above imply that oral exposure to PET microplastics could be a new risk factor for the development of diabetes.