4.7 Article

Exposure to polystyrene microplastics reduces regeneration and growth in planarians

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 432, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2022.128673

Keywords

Planarian; Microplastic; Stem cell; Toxicity; Regeneration

Funding

  1. National Key Research and Development Program of China [2021YFC2301500]
  2. National Nat-ural Science Foundation of China [91543132, 21806056]
  3. Guangdong Natural Science Foundation [2016A030313089]

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This study revealed the adverse effects of polystyrene microplastics (PS-MPs) exposure on the growth, regeneration, and stem cell functions in planarians. The activation of TGF beta/SMAD4 and Notch signaling pathways may be involved in these effects.
The potential adverse effects of microplastics (MPs) on ecosystems and human health have received much attention in recent years. However, only limited data are available on the mechanisms for the uptake, distri-bution, and effects of MPs in freshwater organisms, especially with respect to tissue repair, regeneration and impairment of stem cell functions. To address this knowledge gap, we conducted exposure experiments in which planarians (Dugesia japonica) were exposed to polystyrene (PS)-MPs mixed in liver homogenate and examined the tissue growth and regeneration, stem cell functions, and oxidative stress. The body and blastema areas decreased upon exposure to PS-MPs, indicating that the growth and regeneration of planarians were delayed. The prolif-eration and differentiation processes of stem cells were inhibited, and the proportion of mitotic stem cells decreased, which may be related to the activation of the TGF beta/SMAD4 and Notch signaling pathways. The enhancement of antioxidant enzyme activities and malondialdehyde on the first day of exposure to PS-MPs confirmed the oxidative stress response of planarians to PS-MPs. The present study demonstrated the likelihood of biotoxicity induced by PS-MPs. These results will provide clues for further investigations into the potential risks of PS-MPs to human stem cells.

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