Effects of perfluorinated alkyl acids on cellular responses of MCF-10A mammary epithelial cells in monolayers and on acini formation in vitro

Toxicol Lett. 2016 Sep 30:259:95-107. doi: 10.1016/j.toxlet.2016.08.004. Epub 2016 Aug 7.

Abstract

Perfluorinated alkyl acids (PFAAs) are stable chemicals detected in tissue and serum from various species, including humans, and have been linked to adverse health outcomes. Experimental PFAA exposure in rodents has been associated with changes in mammary gland development. The estrogen receptor (ER)-negative human breast epithelial cell line, MCF-10A, can be grown as monolayer, but also has the ability to form three-dimensional acini in vitro, reflecting aspects of mammary glandular morphogenesis. Cells were exposed to five different PFAAs, perfluorooctane sulfonate (PFOS), perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), perfluorodecanoic acid (PFDA), and perfluoroundecanoic acid (PFUnDA), both in monolayer and acini cultures. In monolayer cultures only the higher concentrations of PFOS, PFNA and PFDA (400-500μM) caused a significant increase in cell death, whereas PFOA and PFUnDA had no effect. Normal acini maturation was negatively impacted by PFOS, PFNA and PFDA already at the lowest concentration tested (0.6μM). Observed effects included loss of organization of the cell clusters and absence of a hollow lumen. Overall, this study demonstrated that PFAAs can interfere with cellular events related to normal development of glandular breast tissue through ER-independent mechanisms.

Keywords: Epithelial polarisation; GM130; Perfluorodecanoic acid; Perfluorononanoic acid; Perfluorooctane sulfonate; Perfluorooctanoic acid; Perfluoroundecanoic acid; Persistent organic pollutants; β-Catenin.

MeSH terms

  • Acinar Cells / drug effects*
  • Acinar Cells / physiology
  • Cell Culture Techniques
  • Cell Cycle / drug effects
  • Cell Death / drug effects
  • Cell Line
  • Epithelial Cells / drug effects*
  • Female
  • Fluorocarbons / toxicity*
  • Humans
  • Mammary Glands, Human / cytology*

Substances

  • Fluorocarbons