Elevated circulating hepcidin levels have been reported in patients with pulmonary artery hypertension (PAH). Hepcidin has been shown to promote proliferation of human pulmonary artery smooth muscle cells (PASMCs) in vitro, suggesting a potential role in PAH pathogenesis. However, the role of human pulmonary artery endothelial cells (PAECs) as either a source of hepcidin, or the effect of hepcidin on PAEC function is not as well described. The objective of this study was to define the role of the hepcidin-ferroportin axis on the phenotype of PAEC and to study potential PAEC-PASMC interactions relevant to the pathogenesis of pulmonary vascular remodeling and PAH. PAECs treated with hepcidin, or interleukin-6 were investigated for both ferroportin and hepcidin release and regulation using immunofluorescence, mRNA levels and cellular release assays. Effects of hepcidin on PASMC and PAEC mitochondrial function was investigated using immunofluorescence and seahorse assay. Migration and proliferation of PASMCs treated with conditioned media from hPAEC treated with hepcidin was investigated using the xCELLigence system and other tools. We demonstrate in this study that PAECs express ferroportin; hepcidin treatment of PAECs resulted in mitochondrial iron accumulation and intracellular hepcidin biosynthesis and release. Conditioned media from hepcidin treated PAECs caused PASMCs to down-regulate ferroportin expression whilst promoting migration and proliferation. Inhibition of hepcidin in PAEC conditioned media limited these responses. PASMC cellular and mitochondrial iron retention are associated with migratory and proliferative responses. This study confirms that the hepcidin ferroportin axis is present and operational in PAECs. Modulation of this axis shows distinct differences in responses seen between PAECS and PASMCs. Stimulation of this axis in PAECs with hepcidin may well institute proliferative and migratory responses in PASMCs of relevance to pathogenesis of PAH offering potential novel therapeutic targets.
Sandy coastal beaches are an important nesting habitat for marine turtles and a known sink for plastic pollution. Existing methodologies for monitoring the spatiotemporal patterns of abundance and composition of plastic are, however, disparate. We engaged a global network of marine turtle scientists to implement a large-scale sampling effort to assess microplastic abundance in beach sediments on marine turtle nesting beaches. Sand samples were collected from 209 sites spanning six oceans, microplastics (1-5 mm) were extracted through stacked sieves, visually identified, and a sub-sample verified via Fourier-transform infrared spectroscopy. Microplastics were detected in 45 % (n = 94) of beaches and within five ocean basins. Microplastic presence and abundance was found to vary markedly within and among ocean basins, with the highest proportion of contaminated beaches found in the Mediterranean (80 %). We present all data in an accessible, open access format to facilitate the extension of monitoring efforts and empower novel analytical approaches.