778 research outputs found

    Magnetic fluctuations and superconductivity in Fe pnictides probed by electron spin resonance

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    The electron spin resonance absorption spectrum of Eu^{2+} ions serves as a probe of the normal and superconducting state in Eu_{0.5}K_{0.5}Fe_2As_2. The spin-lattice relaxation rate 1/T_1^{\rm ESR} obtained from the ESR linewidth exhibits a Korringa-like linear increase with temperature above T_C evidencing a normal Fermi-liquid behavior. Below 45 K deviations from the Korringa-law occur which are ascribed to enhanced magnetic fluctuations within the FeAs layers upon approaching the superconducting transition. Below T_C the spin-lattice relaxation rate 1/T_1^{\rm ESR} follows a T^{1.5}-behavior without the appearance of a coherence peak.Comment: 5 pages, 5 figure

    Structure and Reproduction of Chrysophaeum Lewisii

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/42887/1/10750_2004_Article_BF00045415.pd

    Comparative Approach to Define Increased Regulatory T Cells in Different Cancer Subtypes by Combined Assessment of CD127 and FOXP3

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    In recent years an increase of functional CD4+CD25+ regulatory T cells (Treg cells) has been established for patients with solid tumors, acute leukemias, and lymphomas. We have reported an expanded pool of CD4+CD25high Treg cells in patients with chronic lymphatic leukemia (CLL), multiple myeloma (MM) as well as its premalignant precursor monoclonal gammopathy of undetermined significance (MGUS). In healthy individuals, low-level expression of CD127 on T cells in addition to the expression of FOXP3 has been associated with Treg cells. Here, we demonstrate that the expanded FOXP3+ T-cell population in patients with colorectal cancer, CLL, MGUS, MM, follicular lymphoma, and Hodgkin's disease are exclusively CD127low Treg cells and were strongly suppressive. A significant portion of CD127lowFOXP3+ Treg cells expressed only low levels of CD25 suggesting that the previously reported expansion of CD25+ Treg cells underestimates the true expansion. The assessment of CCR7 and CD45RA expression on the expanded CD4+CD127lowFOXP3+ Treg cells revealed an increase of both naïve as well as central and effector memory Treg cells in peripheral blood. Our data strongly support superiority of combined CD127 and FOXP3 analysis in comparison to CD25 and FOXP3 assessment for further quantification of Treg cells in malignant diseases

    Electron spin resonance in Eu based Fe pnictides

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    The phase diagrams of EuFe2x_{2-x}Cox_xAs2_2 (0x0.4)(0 \leq x \leq 0.4) and EuFe2_2As2y_{2-y}Py_y (0y0.43)(0 \leq y \leq 0.43) are investigated by Eu2+^{2+} electron spin resonance (ESR) in single crystals. From the temperature dependence of the linewidth ΔH(T)\Delta H(T) of the exchange narrowed ESR line the spin-density wave (SDW) (T<TSDW)(T < T_{\rm SDW}) and the normal metallic regime (T>TSDW)(T > T_{\rm SDW}) are clearly distinguished. At T>TSDWT > T_{\rm SDW} the isotropic linear increase of the linewidth is driven by the Korringa relaxation which measures the conduction-electron density of states at the Fermi level. For T<TSDWT < T_{\rm SDW} the anisotropy probes the local ligand field, while the coupling to the conduction electrons disappears. With increasing substitution xx or yy the transition temperature TSDWT_{\rm SDW} decreases linearly accompanied by a linear decrease of the Korringa-relaxation rate from 8 Oe/K at x=y=0x=y=0 down to 3 Oe/K at the onset of superconductivity at x0.2x \approx 0.2 or at y0.3y \approx 0.3, above which it remains nearly constant. Comparative ESR measurements on single crystals of the Eu diluted SDW compound Eu0.2_{0.2}Sr0.8_{0.8}Fe2_2As2_2 and superconducting (SC) Eu0.22_{0.22}Sr0.78_{0.78}Fe1.72_{1.72}Co0.28_{0.28}As2_2 corroborate the leading influence of the ligand field on the Eu2+^{2+} spin relaxation in the SDW regime as well as the Korringa relaxation in the normal metallic regime. Like in Eu0.5_{0.5}K0.5_{0.5}Fe2_2As2_2 a coherence peak is not detected in the latter compound at Tc=21T_{\rm c}=21 K, which is in agreement with the expected complex anisotropic SC gap structure

    Long-Term Signs of T Cell and Myeloid Cell Activation After Intestinal Transplantation With Cellular Rejections Contributing to Further Increase of CD16+ Cell Subsets

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    The intestine mediates a delicate balance between tolerogenic and inflammatory immune responses. The continuous pathogen encounter might also augment immune cell responses contributing to complications observed upon intestinal transplantation (ITx). We thus hypothesized that ITx patients show persistent signs of immune cell activation affecting both the adaptive and innate immune cell compartment. Information on the impact of intestinal grafts on immune cell composition, however, especially in the long-term is sparse. We here assessed activated and differentiated adaptive and innate immune subsets according to time, previous experience of cellular or antibody-mediated rejections or type of transplant after ITx applying multi-parametric flow cytometry, gene expression, serum cytokine and chemokine profiling. ITx patients showed an increase in CD16 expressing monocytes and myeloid dendritic cells (DCs) compared to healthy controls. This was even detectable in patients who were transplanted more than 10 years ago. Also, conventional CD4+ and CD8+ T cells showed persistent signs of activation counterbalanced by increased activated CCR4+ regulatory T cells. Patients with previous cellular rejections had even higher proportions of CD16+ monocytes and DCs, whereas transplanting higher donor mass with multi-visceral grafts was associated with increased T cell activation. The persistent inflammation and innate immune cell activation might contribute to unsatisfactory results after ITx

    Phase separation in paramagnetic Eu0.6La0.4-xSr xMnO3

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    We investigate the magnetic properties of the system Eu 0.6La0.4-xSrxMnO3 with 0.1≤x≤0.3 by means of magnetic susceptibility and electron spin resonance measurements. Ferromagnetic resonance signals are observed in the paramagnetic regime from above the magnetic ordering temperature TN up to approximately room temperature. This regime is characterized by the coexistence of ferromagnetic entities within the globally paramagnetic phase. The results are compared to the Griffiths scenario reported in La1-xSr xMnO3. © 2011 American Physical Society

    Probing Kinetic Mechanisms of Protein Function and Folding with Time-Resolved Natural and Magnetic Chiroptical Spectroscopies

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    Recent and ongoing developments in time-resolved spectroscopy have made it possible to monitor circular dichroism, magnetic circular dichroism, optical rotatory dispersion, and magnetic optical rotatory dispersion with nanosecond time resolution. These techniques have been applied to determine structural changes associated with the function of several proteins as well as to determine the nature of early events in protein folding. These studies have required new approaches in triggering protein reactions as well as the development of time-resolved techniques for polarization spectroscopies with sufficient time resolution and sensitivity to probe protein structural changes

    Prolonged Graft Survival in Older Recipient Mice Is Determined by Impaired Effector T-Cell but Intact Regulatory T-Cell Responses

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    Elderly organ transplant recipients represent a fast growing segment of patients on the waiting list. We examined age-dependent CD4+ T-cell functions in a wild-type (WT) and a transgenic mouse transplant model and analyzed the suppressive function of old regulatory T-cells. We found that splenocytes of naïve old B6 mice contained significantly higher frequencies of T-cells with an effector/memory phenotype (CD4+CD44highCD62Llow). However, in-vitro proliferation (MLR) and IFNγ-production (ELISPOT) were markedly reduced with increasing age. Likewise, skin graft rejection was significantly delayed in older recipients and fewer graft infiltrating CD4+T-cells were observed. Old CD4+ T-cells demonstrated a significant impaired responsiveness as indicated by diminished proliferation and activation. In contrast, old alloantigen-specific CD4+CD25+FoxP3+ T-cells demonstrated a dose-dependent well-preserved suppressor function. Next, we examined characteristics of 18-month old alloreactive T-cells in a transgenic adoptive transfer model. Adoptively transferred old T-cells proliferated significantly less in response to antigen. Skin graft rejection was significantly delayed in older recipients, and graft infiltrating cells were reduced. In summary, advanced recipient age was associated with delayed acute rejection and impaired CD4+ T-cell function and proliferation while CD4+CD25+FoxP3+ T-cells (Tregs) showed a well-preserved function

    Continental-scale geographic change across zealandia during paleogene subduction initiation

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    Data from International Ocean Discovery Program (IODP) Expedition 371 reveal vertical movements of 1-3 km in northern Zealandia during early Cenozoic subduction initiation in the western Pacific Ocean. Lord Howe Rise rose from deep (~1 km) water to sea level and subsided back, with peak uplift at 50 Ma in the north and between 41 and 32 Ma in the south. The New Caledonia Trough subsided 2-3 km between 55 and 45 Ma. We suggest these elevation changes resulted from crust delamination and mantle flow that led to slab formation. We propose a "subduction resurrection" model in which (1) a subduction rupture event activated lithospheric-scale faults across a broad region during less than ~5 m.y., and (2) tectonic forces evolved over a further 4-8 m.y. as subducted slabs grew in size and drove plate-motion change. Such a subduction rupture event may have involved nucleation and lateral propagation of slip-weakening rupture along an interconnected set of preexisting weaknesses adjacent to density anomalies
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