1. Academic Validation
  2. Enhanced toxic effects of photoaged microplastics on the trophoblast cells

Enhanced toxic effects of photoaged microplastics on the trophoblast cells

  • Toxicol Lett. 2025 Jun:409:32-41. doi: 10.1016/j.toxlet.2025.04.010.
Yan Zhang 1 Zijie Zhou 1 Xiaoli Wang 2 Shouhai Jiao 3 Qingshan Zhang 3 Shuai Bao 3 Shuping Zhang 1 Li Sun 4 Xiaolu Li 5
Affiliations

Affiliations

  • 1 The First Affiliated Hospital of Shandong First Medical University, Jinan, Shandong 250014, China; Biomedical Sciences College & Shandong Medicinal Biotechnology Centre, Shandong First Medical University, Jinan, Shandong 250117, China.
  • 2 Endocrinology department, The Fifth People' s Hospital of Jinan, Jinan, Shandong 250022, China.
  • 3 The First Affiliated Hospital of Shandong First Medical University, Jinan, Shandong 250014, China.
  • 4 The First Affiliated Hospital of Shandong First Medical University, Jinan, Shandong 250014, China. Electronic address: sl871204@126.com.
  • 5 The First Affiliated Hospital of Shandong First Medical University, Jinan, Shandong 250014, China. Electronic address: lixiaolu007@hotmail.com.
Abstract

Microplastics (MPs) are emerging as a novel pollutant, raising significant concerns regarding their adverse effects on human health. Furthermore, MPs are susceptible to light-induced aging in the environment, which alters their physical characteristics and potentially alters their toxic effects. While previous studies have documented the retention of MPs in the placenta, the specific impacts of MPs, particularly aged MPs, on placental function remain poorly understood. In the current study, we utilized 1 µm polystyrene microplastics (PS-MPs), a widely used model for MPs, to evaluate the effects of photoaged MPs on the placenta. Following oral administration of PS-MPs beginning on embryonic day 3.5 (E3.5), we observed impaired fetal growth and damage to the placental labyrinth chorionic layer in the treated pregnant mice by embryonic day 13.5 (E13.5). The photoaged PS-MPs were generated by exposure to simulated lighting for 7 or 14 days, resulting in alterations to their physical properties. Notably, enhanced cytotoxicity in trophoblast cells was observed for photoaged PS-MPs compared to pristine PS-MPs. Mechanistically, the altered physical properties of PS-MPs, along with elevated lipid peroxidation, may contribute to the increased cytotoxicity of the photoaged MPs. Our findings provide new insights into the detrimental effects and underlying mechanisms of both MPs and, in particular, aged MPs on the placenta and embryonic development. These insights are crucial for assessing the risks posed by MPs to human pregnancy.

Keywords

Lipid peroxidation; Microplastics; Photoaging; Placental trophoblast cells.

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