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Small airway epithelial cells exposure to printer-emitted engineered nanoparticles induces cellular effects on human microvascular endothelial cells in an alveolar-capillary co-culture model.

Sisler JD; Pirela SV; Friend S; Farcas M; Schwegler-Berry D; Shvedova A; Castranova V; Demokritou P; Qian Y

Nanotoxicology 2015 Aug; 9(6):769-779

https://doi.org/10.3109/17435390.2014.976603

20045367

The printer is one of the most common office equipment. Recently, it was reported that toner formulations for printing equipment constitute nano-enabled products (NEPs) and contain engineered nanomaterials (ENMs) that become airborne during printing. To date, insufficient research has been performed to understand the potential toxicological properties of printer-emitted particles (PEPs) with several studies using bulk toner particles as test particles. These studies demonstrated the ability of toner particles to cause chronic inflammation and fibrosis in animal models. However, the toxicological implications of inhalation exposures to ENMs emitted from laser printing equipment remain largely unknown. The present study investigates the toxicological effects of PEPs using an in vitro alveolar-capillary co-culture model with Human Small Airway Epithelial Cells (SAEC) and Human Microvascular Endothelial Cells (HMVEC). Our data demonstrate that direct exposure of SAEC to low concentrations of PEPs (0.5 and 1.0 mg/mL) caused morphological changes of actin remodeling and gap formations within the endothelial monolayer. Furthermore, increased production of reactive oxygen species (ROS) and angiogenesis were observed in the HMVEC. Analysis of cytokine and chemokine levels demonstrates that interleukin (IL)-6 and MCP-1 may play a major role in the cellular communication observed between SAEC and HMVEC and the resultant responses in HMVEC. These data indicate that PEPs at low, non-cytotoxic exposure levels are bioactive and affect cellular responses in an alveolar-capillary co-culture model, which raises concerns for potential adverse health effects.

Nanotechnology; Printers; Office-equipment; Chemical-composition; Airborne-particles; Chronic-inflammation; Fibrosis; Inhalation-studies; Analytical-models; In-vitro-study; Alveolar-cells; Lung-cells; Morphology; Cellular-function; Cellular-reactions; Bioactivation; Author Keywords: Laser printer emissions; nanotoxicology; occupational health

Dr. Philip Demokritou, PhD, Department of Environmental Health, Harvard School of Public Health, Harvard University, Boston, MA 02115, USA

NANOGK

20150801

Journal Article

pdemokri@hsph.harvard.edu

2015

M112014

6

1743-5390

HELD

Manufacturing

Nanotoxicology

WV; MA