TY - JOUR
T1 - Polystyrene and polyethylene terephthalate nanoplastics differentially impact mouse ovarian follicle function
AU - Alahmadi, Hanin
AU - Nadeem, Maira
AU - Pujols, Alixs M.
AU - Reynolds, Raulle
AU - Islam, Mohammad Saiful
AU - Gupta, Indrani
AU - Potts, Courtney
AU - Harbolic, Allison
AU - Lafontant, Gania
AU - Mitra, Somenath
AU - Warner, Genoa R.
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025/12/1
Y1 - 2025/12/1
N2 - Exposure to micro- and nanoplastics is unavoidable. Foods and beverages contain plastic particles from environmental contamination and processing and packaging materials, which are frequently made of polyethylene terephthalate (PET). Micro- and nanoplastics have been detected in human tissues such as the brain, liver, and placenta, as well as in ovarian follicular fluid, but little is known about the effects nanoplastics have on the female reproductive system. In addition, few studies on the health impacts of nanoplastics have been performed using environmentally relevant plastic types and concentrations. Thus, this research tested the hypothesis that nanoplastics made of spherical polystyrene (PS), a common model nanoplastic, would have different effects on cultured mouse ovarian follicles compared to secondary PET nanoplastics at environmentally relevant doses. The ovary is a highly sensitive reproductive organ responsible for the development of follicles, which contain the oocyte, and production of steroid hormones. Follicles were harvested from adult mouse ovaries and cultured for 96 h with vehicle, spherical commercially available 220 nm PS nanoplastics (1–100 μg/mL), or lab-generated 240 nm PET nanoplastics (0.1–10 μg/mL). PS and PET nanoplastic exposure inhibited follicle growth and altered expression of genes related to steroid synthesis, cell cycle, and oxidative stress. PET nanoplastics increased levels of pregnenolone and decreased expression of Cyp17a1. Overall, both plastic types altered ovarian function, but they impacted different genes in similar pathways. These findings suggest that nanoplastic exposure at environmentally relevant concentrations may pose a risk to female reproductive health by disrupting hormonal and molecular pathways. In addition, environmentally relevant plastic types and doses are necessary for studying health impacts of nanoplastics.
AB - Exposure to micro- and nanoplastics is unavoidable. Foods and beverages contain plastic particles from environmental contamination and processing and packaging materials, which are frequently made of polyethylene terephthalate (PET). Micro- and nanoplastics have been detected in human tissues such as the brain, liver, and placenta, as well as in ovarian follicular fluid, but little is known about the effects nanoplastics have on the female reproductive system. In addition, few studies on the health impacts of nanoplastics have been performed using environmentally relevant plastic types and concentrations. Thus, this research tested the hypothesis that nanoplastics made of spherical polystyrene (PS), a common model nanoplastic, would have different effects on cultured mouse ovarian follicles compared to secondary PET nanoplastics at environmentally relevant doses. The ovary is a highly sensitive reproductive organ responsible for the development of follicles, which contain the oocyte, and production of steroid hormones. Follicles were harvested from adult mouse ovaries and cultured for 96 h with vehicle, spherical commercially available 220 nm PS nanoplastics (1–100 μg/mL), or lab-generated 240 nm PET nanoplastics (0.1–10 μg/mL). PS and PET nanoplastic exposure inhibited follicle growth and altered expression of genes related to steroid synthesis, cell cycle, and oxidative stress. PET nanoplastics increased levels of pregnenolone and decreased expression of Cyp17a1. Overall, both plastic types altered ovarian function, but they impacted different genes in similar pathways. These findings suggest that nanoplastic exposure at environmentally relevant concentrations may pose a risk to female reproductive health by disrupting hormonal and molecular pathways. In addition, environmentally relevant plastic types and doses are necessary for studying health impacts of nanoplastics.
KW - Endocrine disruption
KW - Nanoplastics
KW - Ovary
KW - Polyethylene terephthalate
KW - Women's health
UR - https://www.scopus.com/pages/publications/105018122149
UR - https://www.scopus.com/pages/publications/105018122149#tab=citedBy
U2 - 10.1016/j.envpol.2025.127228
DO - 10.1016/j.envpol.2025.127228
M3 - Article
C2 - 41072712
AN - SCOPUS:105018122149
SN - 0269-7491
VL - 386
JO - Environmental Pollution
JF - Environmental Pollution
M1 - 127228
ER -