60 research outputs found

    Decellularized Matrix from Tumorigenic Human Mesenchymal Stem Cells Promotes Neovascularization with Galectin-1 Dependent Endothelial Interaction

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    BACKGROUND: Acquisition of a blood supply is fundamental for extensive tumor growth. We recently described vascular heterogeneity in tumours derived from cell clones of a human mesenchymal stem cell (hMSC) strain (hMSC-TERT20) immortalized by retroviral vector mediated human telomerase (hTERT) gene expression. Histological analysis showed that cells of the most vascularized tumorigenic clone, -BD11 had a pericyte-like alpha smooth muscle actin (ASMA+) and CD146+ positive phenotype. Upon serum withdrawal in culture, -BD11 cells formed cord-like structures mimicking capillary morphogenesis. In contrast, cells of the poorly tumorigenic clone, -BC8 did not stain for ASMA, tumours were less vascularized and serum withdrawal in culture led to cell death. By exploring the heterogeneity in hMSC-TERT20 clones we aimed to understand molecular mechanisms by which mesenchymal stem cells may promote neovascularization. METHODOLOGY/PRINCIPAL FINDINGS: Quantitative qRT-PCR analysis revealed similar mRNA levels for genes encoding the angiogenic cytokines VEGF and Angiopoietin-1 in both clones. However, clone-BD11 produced a denser extracellular matrix that supported stable ex vivo capillary morphogenesis of human endothelial cells and promoted in vivo neovascularization. Proteomic characterization of the -BD11 decellularized matrix identified 50 extracellular angiogenic proteins, including galectin-1. siRNA knock down of galectin-1 expression abrogated the ex vivo interaction between decellularized -BD11 matrix and endothelial cells. More stable shRNA knock down of galectin-1 expression did not prevent -BD11 tumorigenesis, but greatly reduced endothelial migration into -BD11 cell xenografts. CONCLUSIONS: Decellularized hMSC matrix had significant angiogenic potential with at least 50 angiogenic cell surface and extracellular proteins, implicated in attracting endothelial cells, their adhesion and activation to form tubular structures. hMSC -BD11 surface galectin-1 expression was required to bring about matrix-endothelial interactions and for xenografted hMSC -BD11 cells to optimally recruit host vasculature

    Error analysis and field correction methods in superconducting undulators

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    In Free Electron Lasers (FEL), the electron trajectory through the undulator must meet stringent requirements in terms of trajectory wander and phase variation. This paper analyzes the feasibility of using line current pairs as correctors for superconducting undulators given a set of expected fabrication errors. A tolerance study has first been performed to investigate the impact of geometrical errors on the field quality. These errors are corrected with line currents that increase or decrease the magnetic field locally. Once the uncorrected trajectory is known, an algorithm finds the minimum number of correctors required to fulfill the trajectory specifications, and gives the corrector locations. All the correctors can be powered with the same current, greatly simplifying the implementation. The current then offers a degree of freedom to correct the trajectory and can be tuned dynamically as a function of the magnetic deflection

    High-field studies of the slow thermal death of interlayer coherence in quasi-two-dimensional metals

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    The interlayer magnetoresistance sigma(zz) of the organic metal kappa-(BEDT-TTF)(2)Cu(NCS)(2) has been studied in fields B of up to 45 T and at temperatures T from 0.5 K to 50 K. The peak in rho(zz) seen in exactly in-plane fields, a definitive signature of interlayer coherence, remains to Ts exceeding the Anderson criterion for incoherent transport by a factor similar to 25. Angle-dependent magnetoresistance oscillations (AMROs) due to Fermi-surface orbits are suppressed by rising T, with a T-2 dependence suggesting electron-electron scattering
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