112 research outputs found

    Antibodies against CD20 or B-Cell Receptor Induce Similar Transcription Patterns in Human Lymphoma Cell Lines

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    BACKGROUND: CD20 is a cell surface protein exclusively expressed on B cells. It is a clinically validated target for Non-Hodgkin's lymphomas (NHL) and autoimmune diseases. The B cell receptor (BCR) plays an important role for development and proliferation of pre-B and B cells. Physical interaction of CD20 with BCR and components of the BCR signaling cascade has been reported but the consequences are not fully understood. METHODOLOGY: In this study we employed antibodies against CD20 and against the BCR to trigger the respective signaling. These antibodies induced very similar expression patterns of up- and down-regulated genes in NHL cell lines indicating that CD20 may play a role in BCR signaling and vice versa. Two of the genes that were rapidly and transiently induced by both stimuli are CCL3 and CCL4. 4 hours after stimulation the concentration of these chemokines in culture medium reaches a maximum. Spleen tyrosine kinase Syk is a cytoplasmic tyrosine kinase and a key component of BCR signaling. Both siRNA mediated silencing of Syk and inhibition by selective small molecule inhibitors impaired CCL3/CCL4 protein induction after treatment with either anti-CD20 or anti-BCR antibodies. CONCLUSION: Our results suggest that treatment with anti-CD20 antibodies triggers at least partially a BCR activation-like response in NHL cell lines

    Experimental and simulation study of the behaviour and operation modes of MSGC plus GEM detectors

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    CMSA small series production of detector modules made of MicroStrip Gas Counters (MSGC) and a Gas Electron Multiplier (GEM) foil has been exposed to a high-intensity hadron beam. We report about the reproductibility and stability of the detector responses and about the occurrence and consequences of discharges in the detector. The interdependence of the four voltage differences used in the detector has been studied by simulation and with X-ray measurements. Rate dependence of the signal amplitude is observed. The behaviour of the MSGC+GEM is compared to that of a state-of-the-art MSGC. Influence of various parameters on the detector response is investigated

    Measurement of the Ωc0\Omega_c^0 lifetime at Belle II

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    We report on a measurement of the Ωc0\Omega_c^0 lifetime using Ωc0Ωπ+\Omega_c^0 \to \Omega^-\pi^+ decays reconstructed in e+eccˉe^+e^-\to c\bar{c} data collected by the Belle II experiment and corresponding to 207 fb1207~{\rm fb^{-1}} of integrated luminosity. The result, τ(Ωc0)=243±48(stat)±11(syst) fs\rm\tau(\Omega_c^0)=243\pm48( stat)\pm11(syst)~fs, agrees with recent measurements indicating that the Ωc0\Omega_c^0 is not the shortest-lived weakly decaying charmed baryon

    Measurement of the Ωc0\Omega_c^0 lifetime at Belle II

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    We report on a measurement of the Ωc0\Omega_c^0 lifetime using Ωc0Ωπ+\Omega_c^0 \to \Omega^-\pi^+ decays reconstructed in e+eccˉe^+e^-\to c\bar{c} data collected by the Belle II experiment and corresponding to 207 fb1207~{\rm fb^{-1}} of integrated luminosity. The result, τ(Ωc0)=243±48(stat)±11(syst) fs\rm\tau(\Omega_c^0)=243\pm48( stat)\pm11(syst)~fs, agrees with recent measurements indicating that the Ωc0\Omega_c^0 is not the shortest-lived weakly decaying charmed baryon

    Measurement of the Ωc0\Omega_c^0 lifetime at Belle II

    No full text
    We report on a measurement of the Ωc0\Omega_c^0 lifetime using Ωc0Ωπ+\Omega_c^0 \to \Omega^-\pi^+ decays reconstructed in e+eccˉe^+e^-\to c\bar{c} data collected by the Belle II experiment and corresponding to 207 fb1207~{\rm fb^{-1}} of integrated luminosity. The result, τ(Ωc0)=243±48(stat)±11(syst) fs\rm\tau(\Omega_c^0)=243\pm48( stat)\pm11(syst)~fs, agrees with recent measurements indicating that the Ωc0\Omega_c^0 is not the shortest-lived weakly decaying charmed baryon
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