4.8 Article

Repression of autophagy leads to acrosome biogenesis disruption caused by a sub-chronic oral administration of polystyrene nanoparticles

Journal

ENVIRONMENT INTERNATIONAL
Volume 163, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.envint.2022.107220

Keywords

Polystyrene nanoparticles; Male reproductive; Acrosome biogenesis; Autophagy

Funding

  1. National Natural Science Foundation of China [81903358, 81703187, 81602820]
  2. Postdoctoral Research Project of Chongqing Municipality [XmT2020397]
  3. Chongqing Postdoctoral Science Foundation of China [cstc2021 jcyj-bsh0039]
  4. Natural Science Foundation of Chongqing [cstc2020jcyj-msxmX0192, cstc2021jcyj-msxmX0141]
  5. Science and Technology Research Program of Chongqing Municipal Education Commission [KJQN201900419, KJQN 201900421]
  6. Research Program of Basic Research and Frontier Technology of Chongqing Yuzhong district [20200105]
  7. Chongqing Talent Project [CQYC2020058650, CQYC2021058941]

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The study found that polystyrene nanoplastics (PS-NPs) have negative effects on sperm quality and testicular structures in mice, especially in the medium and high dose groups. Acrosome defects in the testes were also confirmed, and autophagy regulation may play a role in these injuries.
As a new widespread contaminant, nanoplastics (NPs) pose a potential risk to human health. Nevertheless, the adverse effects of NPs on the male reproductive system are poorly understood. In this study, we aimed to determine the effects of polystyrene nanoplastics (PS-NPs) (50 nm) on sperm quality, with a focus on the acrosome defects. After 35 days of intragastric administration, sperm quality was decreased and testicular structures were impaired in mice exposed to PS-NPs in both the medium (1.0 mg/kg) and high dose (10 mg/kg) groups. No significant changes were observed in the low dose (0.2 mg/kg) group. Meanwhile, acrosome pa-rameters including acrosome integrity and acrosome reaction were decreased after the administration of PS-NPs. These findings were consistent with the disruption of acrosome biogenesis, as identified by the changed testicular ultrastructure. Additionally, the findings were further validated using seven marker genes (Gba2, Pick1, Gopc, Hrb, Zpbp1, Spaca1 and O19l2) essential for acrosome formation, which showed that two of these genes (Gopc and Oy19l2) were significantly down-regulated. Moreover, repressed autophagy was observed in the testes of PS-NPs-exposed mice based on autophagy-related protein expression. This phenomenon was further verified in GC-2spd cells treated with PS-NPs (50 mu g/mL, 100 mu g/mL, 200 mu g/mL for 24 h). The potential role of autophagy in such acrosome defects was explored by using the autophagy inhibitor 3-methyladenine (3-MA), autophagy activator rapamycin or beclin-1 siRNA. The results showed that Golgi-associated vesicle disorganization was exacerbated with the 3-MA and beclin-1 siRNA pretreatments, but decreased with the rapamycin pretreatment, and the expression of GOPC and DPY19L2 was also altered. These results indicated that autophagy might be involved in the PS-NPs-induced acrosome lesions based on the regulation of two key acrosome-formation proteins, GOPC and DPY19L2. Altogether, our results will provide new insights into the PS-NPs-induced male reproductive impairment.

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