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Within the Broader Approach Program between Europe and Japan for the early realization of fusion with the construction of the JT-60SA tokamak, ENEA, the Italian Agency for New Technologies, Energy and Sustainable Economic Development, was in charge, among others, to supply ten superconducting Toroidal Field (TF) coils for the JT-60SA magnet system. The related procurement started in 2011 and was concluded in 2018 with the delivery of the tenth coil to the Cold Test Facility in France. The construction of each TF coil module consisted of two main phases: manufacturing of the superconducting winding pack and integration in the corresponding casing structure. With all the foreseen modules already completed, this paper provides a critical review of the contract for the manufacturing of the coils highlighting the main difficulties occurred in the different manufacturing steps and evaluating the performances obtained from the measurements taken at the acceptance tests.

Aims We aimed to investigate the effect of PBDEs (47, 99, 209) on cellular events involved in epigenetic modification, inflammation, and epithelial mesenchymal transition (EMT). Materials and methods We studied: 1) ERK1/2 phosphorylation; 2) Enhancer of Zester Homolog 2 (EZH2); 3) Histone H3 tri-methylated in lysine 27 (H3K27me3); 4) K-RAS; 5) silencing disabled homolog 2-interacting protein gene (DAB2IP), 6) let-7a; 7) Muc5AC/Muc5B, and 8) IL-8 in a 3D in vitro model of epithelium obtained with primary Normal Human Bronchial Epithelial cells (pNHBEs) or A549 cell line, chronically exposed to PBDEs (47, 99, 209). Key findings PBDEs (10 nM, 100 nM and 1 μM) increased ERK1/2 phosphorylation, and EZH2, H3K27me3, and K-RAS protein expression, while decreased DAB2IP and Let-7a transcripts in pNHBEs ALI culture. Furthermore PBDEs (47, 99) (100 nM) increased Muc5AC and Muc5B mRNA, and PBDE 47 (100 nM) IL-8 mRNA via EZH2 in pNHBEs. Finally, PBDEs (100 nM) affected EZH2, H3K27me3, K-RAS protein expression, and DAB2IP, Let-7a transcripts and cell invasion in A549 cells. Gsk343 (methyltransferase EZH2 inhibitor) (1 mM) and U0126 (inhibitor of MEK1/2) (10 μM) were used to show the specific effect of PBDEs. Significance PBDE inhalation might promote inflammation/cancer via EZH2 methyltransferase activity and H3K27me3, k-RAS and ERk1/2 involvement, generating adverse health outcomes of the human lung.