51 research outputs found
Shaping a superconducting dome: Enhanced Cooper-pairing versus suppressed phase coherence in coupled aluminum nanograins
Deterministic enhancement of the superconducting (SC) critical temperature
is a long-standing goal in material science. One strategy is engineering
a material at the nanometer scale such that quantum confinement strengthens the
electron pairing, thus increasing the superconducting energy gap , as
was observed for individual nanoparticles. A true phase-coherent SC condensate,
however, can exist only on larger scales and requires a finite phase stiffness
. In the case of coupled aluminium (Al) nanograins, can exceed that of
bulk Al by a factor of three, but despite several proposals the relevant
mechanism at play is not yet understood. Here we use optical spectroscopy on
granular Al to disentangle the evolution of the fundamental SC energy scales,
and , as a function of grain coupling. Starting from well-coupled
arrays, grows with progressive grain decoupling, causing the
increasing of . As the grain-coupling is further suppressed,
saturates while decreases, concomitantly with a sharp decline of .
This crossover to a phase-driven SC transition is accompanied by an optical gap
persisting above . These findings identify granular Al as an ideal
playground to test the basic mechanisms that enhance superconductivity by
nano-inhomogeneity.Comment: 6 + 6 pages (manuscript + supplementary material
THz conductivity of SrCaRuO
We investigate the optical conductivity of SrCaRuO across the
ferromagnetic to paramagnetic transition that occurs at . The thin films
were grown by metalorganic aerosol deposition with onto
NdGaO substrates. We performed THz frequency domain spectroscopy in a
frequency range from 3~cm to 40~cm (100~GHz to 1.4~THz) and at
temperatures ranging from 5~K to 300~K, measuring transmittivity and phase
shift through the films. From this we obtained real and imaginary parts of the
optical conductivity. The end-members, ferromagnetic SrRuO and paramagnetic
CaRuO, show a strongly frequency-dependent metallic response at
temperatures below 20~K. Due to the high quality of these samples we can access
pronounced intrinsic electronic contributions to the optical scattering rate,
which at 1.4~THz exceeds the residual scattering rate by more than a factor of
three. Deviations from a Drude response start at about 0.7~THz for both
end-members in a remarkably similar way. For the intermediate members a higher
residual scattering originating in the compositional disorder leads to a
featureless optical response, instead. The relevance of low-lying interband
transitions is addressed by a calculation of the optical conductivity within
density functional theory in the local density approximation (LDA)
Optical signatures of the superconducting Goldstone mode in granular aluminum: experiments and theory
Recent advances in the experimental growth and control of disordered thin
films, heterostructures, and interfaces provide a fertile ground for the
observation and characterisation of the collective superconducting excitations
emerging below after breaking the gauge symmetry. Here we combine
THz experiments in a nano-structured granular Al thin film and theoretical
calculations to demonstrate the existence of optically-active phase modes,
which represent the Goldstone excitations of the broken gauge symmetry. By
measuring the complex transmission trough the sample we identify a sizeable and
temperature-dependent optical sub-gap absorption, which cannot be ascribed to
quasiparticle excitations. A quantitative modelling of this material as a
disordered Josephson array of nano-grains allows us to determine, with no free
parameters, the structure of the spatial inhomogeneities induced by shell
effects. Besides being responsible for the enhancement of the critical
temperature with respect to bulk Al, already observed in the past, this spatial
inhomogeneity provides a mechanism for the optical visibility of the Goldstone
mode. By computing explicitly the optical spectrum of the superconducting phase
fluctuations we obtain a good quantitative description of the experimental
data. Our results demonstrate that nanograins arrays are a promising setting to
study and control the collective superconducting excitations via optical means
The microRNA processing subunit DGCR8 is required for a T cell-dependent germinal center response
We have previously shown that the microRNA (miRNA) processor complex consisting of the RNAse Drosha and the DiGeorge Critical Region (DGCR) 8 protein is essential for B cell maturation. To determine whether miRNA processing is required to initiate T cell-mediated antibody responses, we deleted DGCR8 in maturing B2 cells by crossing a mouse with loxP-flanked DGCR8 alleles with a CD23-Cre mouse. As expected, non-immunized mice showed reduced numbers of mature B2 cells and IgG-secreting cells and diminished serum IgG titers. In accordance, germinal centers and antigen-specific IgG-secreting cells were absent in mice immunized with T-dependent antigens. Therefore, DGCR8 is required to mount an efficient T-dependent antibody response. However, DGCR8 deletion in B1 cells was incomplete, resulting in unaltered B1 cell numbers and normal IgM and IgA titers in DGCR8-knock-out mice. Therefore, this mouse model could be used to analyze B1 responses in the absence of functional B2 cells
Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition)
The third edition of Flow Cytometry Guidelines provides the key aspects to consider when performing flow cytometry experiments and includes comprehensive sections describing phenotypes and functional assays of all major human and murine immune cell subsets. Notably, the Guidelines contain helpful tables highlighting phenotypes and key differences between human and murine cells. Another useful feature of this edition is the flow cytometry analysis of clinical samples with examples of flow cytometry applications in the context of autoimmune diseases, cancers as well as acute and chronic infectious diseases. Furthermore, there are sections detailing tips, tricks and pitfalls to avoid. All sections are written and peer‐reviewed by leading flow cytometry experts and immunologists, making this edition an essential and state‐of‐the‐art handbook for basic and clinical researchers.DFG, 389687267, Kompartimentalisierung, Aufrechterhaltung und Reaktivierung humaner Gedächtnis-T-Lymphozyten aus Knochenmark und peripherem BlutDFG, 80750187, SFB 841: Leberentzündungen: Infektion, Immunregulation und KonsequenzenEC/H2020/800924/EU/International Cancer Research Fellowships - 2/iCARE-2DFG, 252623821, Die Rolle von follikulären T-Helferzellen in T-Helferzell-Differenzierung, Funktion und PlastizitätDFG, 390873048, EXC 2151: ImmunoSensation2 - the immune sensory syste
The intestine: A highly dynamic microenvironment for IgA plasma cells
Pracht K, Wittner J, Kagerer F, Jäck H-M, Schuh W. The intestine: A highly dynamic microenvironment for IgA plasma cells. Frontiers in Immunology. 2023;14.To achieve longevity, IgA plasma cells require a sophisticated anatomical microenvironment that provides cytokines, cell-cell contacts, and nutrients as well as metabolites. The intestinal epithelium harbors cells with distinct functions and represents an important defense line. Anti-microbial peptide-producing paneth cells, mucus-secreting goblet cells and antigen-transporting microfold (M) cells cooperate to build a protective barrier against pathogens. In addition, intestinal epithelial cells are instrumental in the transcytosis of IgA to the gut lumen, and support plasma cell survival by producing the cytokines APRIL and BAFF. Moreover, nutrients are sensed through specialized receptors such as the aryl hydrocarbon receptor (AhR) by both, intestinal epithelial cells and immune cells. However, the intestinal epithelium is highly dynamic with a high cellular turn-over rate and exposure to changing microbiota and nutritional factors. In this review, we discuss the spatial interplay of the intestinal epithelium with plasma cells and its potential contribution to IgA plasma cell generation, homing, and longevity. Moreover, we describe the impact of nutritional AhR ligands on intestinal epithelial cell-IgA plasma cell interaction. Finally, we introduce spatial transcriptomics as a new technology to address open questions in intestinal IgA plasma cell biology
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