141 research outputs found
X-ray Near Field Speckle: Implementation and Critical Analysis
We have implemented the newly-introduced, coherence-based technique of x-ray
near-field speckle (XNFS) at 8-ID-I at the Advanced Photon Source. In the near
field regime of high-brilliance synchrotron x-rays scattered from a sample of
interest, it turns out, that, when the scattered radiation and the main beam
both impinge upon an x-ray area detector, the measured intensity shows
low-contrast speckles, resulting from interference between the incident and
scattered beams. We built a micrometer-resolution XNFS detector with a high
numerical aperture microscope objective and demonstrate its capability for
studying static structures and dynamics at longer length scales than
traditional far field x-ray scattering techniques. Specifically, we
characterized the structure and dynamics of dilute silica and polystyrene
colloidal samples. Our study reveals certain limitations of the XNFS technique,
which we discuss.Comment: 53 pages, 16 figure
Histamine deficiency promotes inflammation-associated carcinogenesis through reduced myeloid maturation and accumulation of CD11b \u3csup\u3e+\u3c/sup\u3eLy6G\u3csup\u3e+\u3c/sup\u3e immature myeloid cells
Histidine decarboxylase (HDC), the unique enzyme responsible for histamine generation, is highly expressed in myeloid cells, but its function in these cells is poorly understood. Here we show that Hdc-knockout mice show a high rate of colon and skin carcinogenesis. Using Hdc-EGFP bacterial artificial chromosome (BAC) transgenic mice in which EGFP expression is controlled by the Hdc promoter, we show that Hdc is expressed primarily in CD11b +Ly6G+ immature myeloid cells (IMCs) that are recruited early on in chemical carcinogenesis. Transplant of Hdc-deficient bone marrow to wild-type recipients results in increased CD11b + Ly6G + cell mobilization and reproduces the cancer susceptibility phenotype of Hdc-knockout mice. In addition, Hdc-deficient IMCs promote the growth of tumor allografts, whereas mouse CT26 colon cancer cells downregulate Hdc expression through promoter hypermethylation and inhibit myeloid cell maturation. Exogenous histamine induces the differentiation of IMCs and suppresses their ability to support the growth of tumor allografts. These data indicate key roles for Hdc and histamine in myeloid cell differentiation and CD11b+Ly6G+IMCs in early cancer development. © 2011 Nature America, Inc. All rights reserved
Direct measurement of antiferromagnetic domain fluctuations
Measurements of magnetic noise emanating from ferromagnets due to domain
motion were first carried out nearly 100 years ago and have underpinned much
science and technology. Antiferromagnets, which carry no net external magnetic
dipole moment, yet have a periodic arrangement of the electron spins extending
over macroscopic distances, should also display magnetic noise, but this must
be sampled at spatial wavelengths of order several interatomic spacings, rather
than the macroscopic scales characteristic of ferromagnets. Here we present the
first direct measurement of the fluctuations in the nanometre-scale spin-
(charge-) density wave superstructure associated with antiferromagnetism in
elemental Chromium. The technique used is X-ray Photon Correlation
Spectroscopy, where coherent x-ray diffraction produces a speckle pattern that
serves as a "fingerprint" of a particular magnetic domain configuration. The
temporal evolution of the patterns corresponds to domain walls advancing and
retreating over micron distances. While the domain wall motion is thermally
activated at temperatures above 100K, it is not so at lower temperatures, and
indeed has a rate which saturates at a finite value - consistent with quantum
fluctuations - on cooling below 40K. Our work is important because it provides
an important new measurement tool for antiferromagnetic domain engineering as
well as revealing a fundamental new fact about spin dynamics in the simplest
antiferromagnet.Comment: 19 pages, 4 figure
Seismic anisotropy in the mantle of a tectonically inverted extensional basin: A shear-wave splitting and mantle xenolith study on the western Carpathian-Pannonian region
Information on seismic anisotropy in the Earth's mantle can be obtained from (1) shear-wave splitting analyses which allow to distinguish single or multi-layered anisotropy and delay time of the fast and slow polarized wave can indicate its thickness, and (2) studying mantle peridotites where seismic properties can be inferred from lattice preferred orientation of deformed minerals. We provide a detailed shear-wave splitting map of the western part of the Carpathian-Pannonian region (CPR), an extensional basin recently experiencing tectonic inversion, using splitting data. We then compare the results with seismic properties reported from mantle xenoliths to characterize the depth, thickness, and regional differences of the anisotropic layer in the mantle. Mantle anisotropy is different in the northern and the central/southern part of the western CPR. In the northern part, the lack of azimuthal dependence of the fast split S-wave indicates a single anisotropic layer, which agrees with xenolith data from the Nógrád-Gömör volcanic field. Systematic azimuthal variations in several stations in the central areas point to multiple anisotropic layers, which may be explained by two distinct xenolith subgroups described in the Bakony-Balaton Highland. The shallower layer probably has a ‘fossilized’ lithospheric structure, representing former asthenospheric flow, whereas the deeper one reflects structures attributed to present-day convergent tectonics, also observed in the regional NW-SE fast S-wave orientations. In the Styrian Basin at the western rim of the CPR, results are ambiguous as shear-wave splitting data hint at the presence of multiple anisotropic layers. Spatial coherency analysis of the splitting parameters places the center of the anisotropic layer at ~140–150 km depth under the Western Carpathians, which implies a total thickness of ~220–240 km. Thicknesses estimated from seismic properties of xenoliths give lower values, pointing to heterogeneously distributed anisotropy or different orientation of the mineral deformation structures
Improved circulating microparticle analysis in acid-citrate dextrose (ACD) anticoagulant tube.
INTRODUCTION: Recently extracellular vesicles (exosomes, microparticles also referred to as microvesicles and apoptotic bodies) have attracted substantial interest as potential biomarkers and therapeutic vehicles. However, analysis of microparticles in biological fluids is confounded by many factors such as the activation of cells in the blood collection tube that leads to in vitro vesiculation. In this study we aimed at identifying an anticoagulant that prevents in vitro vesiculation in blood plasma samples. MATERIALS AND METHODS: We compared the levels of platelet microparticles and non-platelet-derived microparticles in platelet-free plasma samples of healthy donors. Platelet-free plasma samples were isolated using different anticoagulant tubes, and were analyzed by flow cytometry and Zymuphen assay. The extent of in vitro vesiculation was compared in citrate and acid-citrate-dextrose (ACD) tubes. RESULTS: Agitation and storage of blood samples at 37 degrees C for 1hour induced a strong release of both platelet microparticles and non-platelet-derived microparticles. Strikingly, in vitro vesiculation related to blood sample handling and storage was prevented in samples in ACD tubes. Importantly, microparticle levels elevated in vivo remained detectable in ACD tubes. CONCLUSIONS: We propose the general use of the ACD tube instead of other conventional anticoagulant tubes for the assessment of plasma microparticles since it gives a more realistic picture of the in vivo levels of circulating microparticles and does not interfere with downstream protein or RNA analyses
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