Upregulation of epithelial metallothioneins by metal-rich ultrafine particulate matter from an underground railway

Author:

Loxham Matthew1234ORCID,Woo Jeongmin1,Singhania Akul1,Smithers Natalie P1,Yeomans Alison5,Packham Graham5,Crainic Alina M6,Cook Richard B6,Cassee Flemming R78,Woelk Christopher H1ORCID,Davies Donna E123

Affiliation:

1. School of Clinical and Experimental Sciences, University of Southampton Faculty of Medicine, University Hospital Southampton, Tremona Road, Southampton, UK, SO16 6YD

2. NIHR Southampton Biomedical Research Centre, University Hospital Southampton, Tremona Road, Southampton, UK, SO16 6YD

3. Institute for Life Sciences, Highfield Campus, University of Southampton, Southampton, UK, SO17 1BJ

4. Southampton Marine and Maritime Institute, University of Southampton, Boldrewood Innovation Campus, Southampton, UK, SO16 7QF

5. Cancer Research UK Centre, Cancer Sciences, University of Southampton Faculty of Medicine, University Hospital Southampton, Southampton, UK, SO16 6YD

6. National Centre for Advanced Tribology (nCATS), Mechanical Engineering, Faculty of Engineering and Physical Sciences, University of Southampton, Southampton, UK, SO17 1BJ

7. Centre for Sustainability, Environment, and Health, National Institute for Public Health and the Environment (RIVM), Bilthoven, The Netherlands

8. Institute for Risk Assessment Sciences (IRAS), Utrecht University, Utrecht, The Netherlands

Abstract

Abstract Airborne particulate matter (PM) is a leading cause of mortality and morbidity. However, understanding of the range and mechanisms of effects of PM components is poor. PM generated in underground railways is rich in metals, especially iron. In the ultrafine (UFPM; <0.1 μm diameter) fraction, the combination of small size and metal enrichment poses an unknown health risk. This study aimed to analyse transcriptomic responses to underground UFPM in primary bronchial epithelial cells (PBECs), a key site of PM deposition. The oxidation state of iron in UFPM from an underground station was determined by X-ray absorption near edge structure (XANES) spectroscopy. Antioxidant response was assayed using a reporter cell line transfected with an antioxidant response element (ARE)-luciferase construct. Differentiated PBECs were exposed to UFPM for 6 h or 24 h for RNA-Seq and RT-qPCR analysis. XANES showed predominance of redox-active Fe3O4, with ROS generation confirmed by induction of ARE-luciferase expression. 6 h exposure of PBECs to UFPM identified 52 differentially expressed genes (DEGs), especially associated with epithelial maintenance, whereas 24 h exposure yielded 23 DEGs, particularly involved with redox homeostasis and metal binding. At both timepoints, there was upregulation of members of the metallothionein family, low molecular weight proteins with antioxidant activity whose main function is binding and homeostasis of zinc and copper ions, but not iron ions. This upregulation was partially inhibited by metal chelation or ROS scavenging. These data suggest differential regulation of responses to metal-rich UFPM depending on exposure period, and highlight novel pathways and markers of PM exposure, with the role of metallothioneins warranting further investigation.

Funder

AAIR Charity

Biotechnology and Biological Sciences Research Council

Publisher

Oxford University Press (OUP)

Subject

Metals and Alloys,Biochemistry,Biomaterials,Biophysics,Chemistry (miscellaneous)

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