Effects of Cyanobacterial Harmful Algal Bloom Toxin Microcystin-LR on Gonadotropin-Dependent Ovarian Follicle Maturation and Ovulation in Mice

Yingzheng Wang, Pawat Pattarawat, Jiyang Zhang, Eunchong Kim, Delong Zhang, Mingzhu Fang, Elizabeth A. Jannaman, Ye Yuan, Saurabh Chatterjee, Ji Yong Julie Kim, Geoffrey I. Scott, Qiang Zhang, Shuo Xiao*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

BACKGROUND: Cyanobacterial harmful algal blooms (CyanoHABs) originate from the excessive growth or bloom of cyanobacteria often referred to as blue-green algae. They have been on the rise globally in both marine and freshwaters in recently years with increasing frequency and severity owing to the rising temperature associated with climate change and increasing anthropogenic eutrophication from agricultural runoff and urbanization. Humans are at a great risk of exposure to toxins released from CyanoHABs through drinking water, food, and recreational activities, making CyanoHAB toxins a new class of contaminants of emerging concern. OBJECTIVES: We investigated the toxic effects and mechanisms of microcystin-LR (MC-LR), the most prevalent CyanoHAB toxin, on the ovary and associated reproductive functions. METHODS: Mouse models with either chronic daily oral or acute intraperitoneal exposure, an engineered three-dimensional ovarian follicle culture system, and human primary ovarian granulosa cells were tested with MC-LR of various dose levels. Single-follicle RNA sequencing, reverse tran-scription–quantitative polymerase chain reaction, enzyme-linked immunosorbent assay, western blotting, immunohistochemistry (IHC), and benchmark dose modeling were used to examine the effects of MC-LR on follicle maturation, hormone secretion, ovulation, and luteinization. RESULTS: Mice exposed long term to low-dose MC-LR did not exhibit any differences in the kinetics of folliculogenesis, but they had significantly fewer corpora lutea compared with control mice. Superovulation models further showed that mice exposed to MC-LR during the follicle maturation window had significantly fewer ovulated oocytes. IHC results revealed ovarian distribution of MC-LR, and mice exposed to MC-LR had significantly lower expression of key follicle maturation mediators. Mechanistically, in both murine and human granulosa cells exposed to MC-LR, there was reduced protein phospha-tase 1 (PP1) activity, disrupted PP1-mediated PI3K/AKT/FOXO1 signaling, and less expression of follicle maturation-related genes. DISCUSSION: Using both in vivo and in vitro murine and human model systems, we provide data suggesting that environmentally relevant exposure to the CyanoHAB toxin MC-LR interfered with gonadotropin-dependent follicle maturation and ovulation. We conclude that MC-LR may pose a nonne-gligible risk to women’s reproductive health by heightening the probability of irregular menstrual cycles and infertility related to ovulatory disorders. https://doi.org/10.1289/EHP12034.

Original languageEnglish (US)
Article number067010
JournalEnvironmental health perspectives
Volume131
Issue number6
DOIs
StatePublished - Jun 2023

Funding

This work was supported by the National Institutes of Health (NIH) K01ES030014 and P30ES005022 to S.X., R01ES032144 to S.X. and Q.Z., P01ES028942 to G.I.S., S.C., and S.X., UH3ES029073 to J.K. and S.X. and by the startup fund from the Environmental and Occupational Health Sciences Institute at Rutgers University to S.X. The manuscript has been subjected to review by the New Jersey Department of Environmental Protection (NJDEP) Division and Science and Research and approved for publication, but the views expressed do not necessarily reflect the views or policy of the NJDEP. Y.W. contributed to the experimental design, data collection and analysis, and manuscript writing. P.P., J.Z., E.K., E.A.J., and D.Z. contributed to the data collection and analysis. M.F., Y.Y., S.C., J-Y.J.K, and G.I.S. contributed to the data interpretation and manuscript writing. Q.Z. contributed to the experimental design, data analysis, and manuscript writing. S.X. conceived of the project, designed experiments, collected, analyzed, and interpreted data, wrote the manuscript, and provided final approval of the manuscript. This work was supported by the National Institutes of Health (NIH) K01ES030014 and P30ES005022 to S.X., R01ES032144 to S.X. and Q.Z., P01ES028942 to G.I.S., S.C., and S.X., UH3ES029073 to J.K. and S.X. and by the startup fund from the Environmental and Occupational Health Sciences Institute at Rutgers University to S.X. The manuscript has been subjected to review by the New Jersey Department of Environmental Protection (NJDEP) Division and Science and Research and approved for publication, but the views expressed do not necessarily reflect the views or policy of the NJDEP.

ASJC Scopus subject areas

  • Public Health, Environmental and Occupational Health
  • Health, Toxicology and Mutagenesis

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