Wein

Ohne Zusammenfassung     

Tabak

Ohne Zusammenfassung     

Congress and the Fusion Energy Sciences Program: A Historical Analysis

This report reviews and analyzes the 42-year history of congressional deliberations over funding of the magnetic fusion research and development (R&D) program. That analysis provides the basis for an assessment about how the program might fare in the future as it proceeds in the direction of developing a long-term energy source from fusion. The assessment is presented as a series of questions that Congress may wish to address in determining the program's future.     

Elaboration of Al2O3/PTFE icephobic coatings for protecting aluminum surfaces

In order to protect aluminum ground wires and phase conductors of overhead power lines against ice adhesion and excessive accretion, for ensuring safe and reliable power transmission during winter periods, a new coating with icephobic characteristics and satisfactory mechanical properties was developed. The method consisted in depositing an extremely adherent poly(tetrafluoroethylene) or PTFE coating on an Al₂O₃ underlayer produced by anodisation in either a phosphoric or an oxalic acid electrolyte. PTFE impregnation was carried out at low temperature (320 °C) and coating adhesion was assessed using tape and bend tests. These treatments resulted in highly hydrophobic surfaces with water contact angles lying between 130° and 140°. Ice shear stress was reduced by almost 2.5 times, and the PTFE coatings remained active after several ice shedding events. Morphologies and chemical compositions were studied using scanning electron microscopy, energy dispersive X-Ray analysis, as well as Fourier Transform Infra Red and X-Ray photoelectron spectroscopy.     

Identification of Structural and Molecular Signatures Mediating Adaptive Changes in the Mouse Kidney in Response to Pregnancy

Pregnancy is characterized by adaptations in the function of several maternal body systems that ensure the development of the fetus whilst maintaining health of the mother. The renal system is responsible for water and electrolyte balance, as well as waste removal. Thus, it is imperative that structural and functional changes occur in the kidney during pregnancy. However, our knowledge of the precise morphological and molecular mechanisms occurring in the kidney during pregnancy is still very limited. Here, we investigated the changes occurring in the mouse kidney during pregnancy by performing an integrated analysis involving histology, gene and protein expression assays, mass spectrometry profiling and bioinformatics. Data from non-pregnant and pregnant mice were used to identify critical signalling pathways mediating changes in the maternal kidneys. We observed an expansion of renal medulla due to proliferation and infiltration of interstitial cellular constituents, as well as alterations in the activity of key cellular signalling pathways (e.g., AKT, AMPK and MAPKs) and genes involved in cell growth/metabolism (e.g., Cdc6, Foxm1 and Rb1) in the kidneys during pregnancy. We also generated plasma and urine proteomic profiles, identifying unique proteins in pregnancy. These proteins could be used to monitor and study potential mechanisms of renal adaptations during pregnancy and disease.     

NKG2C+ NK Cells for Immunotherapy of Glioblastoma Multiforme

In glioblastoma, non-classical human leucocyte antigen E (HLA-E) and HLA-G are frequently overexpressed. HLA-E loaded with peptides derived from HLA class I and from HLA-G contributes to inhibition of natural killer (NK) cells with expression of the inhibitory receptor CD94/NKG2A. We investigated whether NK cells expressing the activating CD94/NKG2C receptor counterpart were able to exert anti-glioma effects. NKG2C+ subsets were preferentially expanded by a feeder cell line engineered to express an artificial disulfide-stabilized trimeric HLA-E ligand (HLA-E*spG). NK cells expanded by a feeder cell line, which facilitates outgrowth of conventional NKG2A+, and fresh NK cells, were included for comparison. Expansion via the HLA-E*spG feeder cells selectively increased the fraction of NKG2C+ NK cells, which displayed a higher frequency of KIR2DL2/L3/S2 and CD16 when compared to expanded NKG2A+ NK cells. NKG2C+ NK cells exhibited increased cytotoxicity against K562 and KIR:HLA-matched and -mismatched primary glioblastoma multiforme (GBM) cells when compared to NKG2A+ NK cells and corresponding fresh NK cells. Cytotoxic responses of NKG2C+ NK cells were even more pronounced when utilizing target cells engineered with HLA-E*spG. These findings support the notion that NKG2C+ NK cells have potential therapeutic value for treating gliomas.