TY - JOUR A1 - Gulbins, Erich A1 - Palmada, Monica A1 - Reichel, Martin A1 - Lueth, Anja A1 - Boehmer, Christoph A1 - Amato, Davide A1 - Mueller, Christian P. A1 - Tischbirek, Carsten H. A1 - Groemer, Teja W. A1 - Tabatabai, Ghazaleh A1 - Becker, Katrin Anne A1 - Tripal, Philipp A1 - Staedtler, Sven A1 - Ackermann, Teresa F. A1 - van Brederode, Johannes A1 - Alzheimer, Christian A1 - Weller, Michael A1 - Lang, Undine E. A1 - Kleuser, Burkhard A1 - Grassme, Heike A1 - Kornhuber, Johannes T1 - Acid sphingomyelinase-ceramide system mediates effects of antidepressant drugs JF - Nature medicine N2 - Major depression is a highly prevalent severe mood disorder that is treated with antidepressants. The molecular targets of antidepressants require definition. We investigated the role of the acid sphingomyelinase (Asm)-ceramide system as a target for antidepressants. Therapeutic concentrations of the antidepressants amitriptyline and fluoxetine reduced Asm activity and ceramide concentrations in the hippocampus, increased neuronal proliferation, maturation and survival and improved behavior in mouse models of stress-induced depression. Genetic Asm deficiency abrogated these effects. Mice overexpressing Asm, heterozygous for acid ceramidase, treated with blockers of ceramide metabolism or directly injected with C16 ceramide in the hippocampus had higher ceramide concentrations and lower rates of neuronal proliferation, maturation and survival compared with controls and showed depression-like behavior even in the absence of stress. The decrease of ceramide abundance achieved by antidepressant-mediated inhibition of Asm normalized these effects. Lowering ceramide abundance may thus be a central goal for the future development of antidepressants. Y1 - 2013 U6 - https://doi.org/10.1038/nm.3214 SN - 1078-8956 VL - 19 IS - 7 SP - 934 EP - + PB - Nature Publ. Group CY - New York ER - TY - JOUR A1 - Schmidt, Sabrina A1 - Saxenhofer, Moritz A1 - Drewes, Stephan A1 - Schlegel, Mathias A1 - Wanka, Konrad M. A1 - Frank, Raphael A1 - Klimpel, Sven A1 - von Blanckenhagen, Felix A1 - Maaz, Denny A1 - Herden, Christiane A1 - Freise, Jona A1 - Wolf, Ronny A1 - Stubbe, Michael A1 - Borkenhagen, Peter A1 - Ansorge, Hermann A1 - Eccard, Jana A1 - Lang, Johannes A1 - Jourdain, Elsa A1 - Jacob, Jens A1 - Marianneau, Philippe A1 - Heckel, Gerald A1 - Ulrich, Rainer Günter T1 - High genetic structuring of Tula hantavirus JF - Archives of virology N2 - Tula virus (TULV) is a vole-associated hantavirus with low or no pathogenicity to humans. In the present study, 686 common voles (Microtus arvalis), 249 field voles (Microtus agrestis) and 30 water voles (Arvicola spec.) were collected at 79 sites in Germany, Luxembourg and France and screened by RT-PCR and TULV-IgG ELISA. TULV-specific RNA and/or antibodies were detected at 43 of the sites, demonstrating a geographically widespread distribution of the virus in the studied area. The TULV prevalence in common voles (16.7 %) was higher than that in field voles (9.2 %) and water voles (10.0 %). Time series data at ten trapping sites showed evidence of a lasting presence of TULV RNA within common vole populations for up to 34 months, although usually at low prevalence. Phylogenetic analysis demonstrated a strong genetic structuring of TULV sequences according to geography and independent of the rodent species, confirming the common vole as the preferential host, with spillover infections to co-occurring field and water voles. TULV phylogenetic clades showed a general association with evolutionary lineages in the common vole as assessed by mitochondrial DNA sequences on a large geographical scale, but with local-scale discrepancies in the contact areas. Y1 - 2016 U6 - https://doi.org/10.1007/s00705-016-2762-6 SN - 0304-8608 SN - 1432-8798 VL - 161 SP - 1135 EP - 1149 PB - Springer CY - Wien ER - TY - JOUR A1 - Abeysekara, A. U. A1 - Archer, A. A1 - Benbow, Wystan A1 - Bird, Ralph A1 - Brill, A. A1 - Brose, Robert A1 - Buchovecky, M. A1 - Calderon-Madera, D. A1 - Christiansen, J. L. A1 - Cui, W. A1 - Daniel, M. K. A1 - Falcone, A. A1 - Feng, Q. A1 - Fernandez-Alonso, M. A1 - Finley, J. P. A1 - Fortson, Lucy A1 - Furniss, Amy A1 - Gent, A. A1 - Giuri, C. A1 - Gueta, O. A1 - Hanna, David A1 - Hassan, T. A1 - Hervet, Oliver A1 - Holder, J. A1 - Hughes, G. A1 - Humensky, T. B. A1 - Johnson, Caitlin A. A1 - Kaaret, P. A1 - Kertzman, M. A1 - Kieda, David A1 - Krause, Maria A1 - Krennrich, F. A1 - Kumar, S. A1 - Lang, M. J. A1 - Maier, Gernot A1 - Moriarty, P. A1 - Mukherjee, Reshmi A1 - Nievas-Rosillo, M. A1 - Ong, R. A. A1 - Pfrang, Konstantin Johannes A1 - Pohl, Martin A1 - Prado, R. R. A1 - Pueschel, Elisa A1 - Quinn, J. A1 - Ragan, K. A1 - Reynolds, P. T. A1 - Ribeiro, D. A1 - Richards, G. T. A1 - Roache, E. A1 - Rovero, A. C. A1 - Sadeh, Iftach A1 - Santander, M. A1 - Sembroski, G. H. A1 - Shahinyan, Karlen A1 - Sushch, Iurii A1 - Svraka, T. A1 - Weinstein, A. A1 - Wells, R. M. A1 - Wilcox, Patrick A1 - Wilhelm, Alina A1 - Williams, David Arnold A1 - Williamson, T. J. A1 - Zitzer, B. T1 - Measurement of the Extragalactic Background Light Spectral Energy Distribution with VERITAS JF - The astrophysical journal : an international review of spectroscopy and astronomical physics N2 - The extragalactic background light (EBL), a diffuse photon field in the optical and infrared range, is a record of radiative processes over the universe?s history. Spectral measurements of blazars at very high energies (>100 GeV) enable the reconstruction of the spectral energy distribution (SED) of the EBL, as the blazar spectra are modified by redshift- and energy-dependent interactions of the gamma-ray photons with the EBL. The spectra of 14 VERITAS-detected blazars are included in a new measurement of the EBL SED that is independent of EBL SED models. The resulting SED covers an EBL wavelength range of 0.56?56 ?m, and is in good agreement with lower limits obtained by assuming that the EBL is entirely due to radiation from cataloged galaxies. KW - Extragalactic astronomy KW - Active galactic nuclei KW - Diffuse radiation KW - Cosmology Y1 - 2019 U6 - https://doi.org/10.3847/1538-4357/ab4817 SN - 0004-637X SN - 1538-4357 VL - 885 IS - 2 PB - IOP Publ. Ltd. CY - Bristol ER - TY - JOUR A1 - Tockhorn, Philipp A1 - Sutter, Johannes A1 - Cruz Bournazou, Alexandros A1 - Wagner, Philipp A1 - Jäger, Klaus A1 - Yoo, Danbi A1 - Lang, Felix A1 - Grischek, Max A1 - Li, Bor A1 - Li, Jinzhao A1 - Shargaieva, Oleksandra A1 - Unger, Eva A1 - Al-Ashouri, Amran A1 - Köhnen, Eike A1 - Stolterfoht, Martin A1 - Neher, Dieter A1 - Schlatmann, Rutger A1 - Rech, Bernd A1 - Stannowski, Bernd A1 - Albrecht, Steve A1 - Becker, Christiane T1 - Nano-optical designs for high-efficiency monolithic perovskite-silicon tandem solar cells JF - Nature nanotechnology N2 - Designing gentle sinusoidal nanotextures enables the realization of high-efficiency perovskite-silicon solar cells
Perovskite-silicon tandem solar cells offer the possibility of overcoming the power conversion efficiency limit of conventional silicon solar cells. Various textured tandem devices have been presented aiming at improved optical performance, but optimizing film growth on surface-textured wafers remains challenging. Here we present perovskite-silicon tandem solar cells with periodic nanotextures that offer various advantages without compromising the material quality of solution-processed perovskite layers. We show a reduction in reflection losses in comparison to planar tandems, with the new devices being less sensitive to deviations from optimum layer thicknesses. The nanotextures also enable a greatly increased fabrication yield from 50% to 95%. Moreover, the open-circuit voltage is improved by 15 mV due to the enhanced optoelectronic properties of the perovskite top cell. Our optically advanced rear reflector with a dielectric buffer layer results in reduced parasitic absorption at near-infrared wavelengths. As a result, we demonstrate a certified power conversion efficiency of 29.80%. Y1 - 2022 U6 - https://doi.org/10.1038/s41565-022-01228-8 SN - 1748-3387 SN - 1748-3395 VL - 17 IS - 11 SP - 1214 EP - 1221 PB - Nature Publishing Group CY - London [u.a.] ER -