Final State Interaction in Exclusive (e,e′NN)(e,e'NN) Reactions

Contributions of nucleon-nucleon (NN) correlations, meson exchange currents and the residual final state interactions (FSI) on exclusive two-nucleon knock-out reactions induced by electron scattering are investigated. All contributions are derived from the same realistic meson exchange model for the NN interaction. Effects of correlations and FSI are determined in a consistent way by solving the NN scattering equation, the Bethe-Goldstone equation, for two nucleons in nuclear matter. One finds that the FSI re-scattering terms are non-negligible even if the two nucleons are emitted back to back.Comment: 8 pages, 5 figure

A model for two-proton emission induced by electron scattering

A model to study two-proton emission processes induced by electron scattering is developed. The process is induced by one-body electromagnetic operators acting together with short-range correlations, and by two-body $\Delta$ currents. The model includes all the diagrams containing a single correlation function. A test of the sensitivity of the model to the various theoretical inputs is done. An investigation of the relevance of the $\Delta$ currents is done by changing the final state angular momentum, excitation energy and momentum transfer. The sensitivity of the cross section to the details of the correlation function is studied by using realistic and schematic correlations. Results for $^{12}$C, $^{16}$O and $^{40}$Ca nuclei are presented.Comment: 30 pages, 18 figures, 3 table

Nucleon-Nucleon Correlations and Two-Nucleon Currents in Exclusive (e,e′NNe,e'NN) Reactions

The contributions of short-range nucleon-nucleon (NN) correlations, various meson exchange current (MEC) terms and the influence of $\Delta$ isobar excitations (isobaric currents, IC) on exclusive two-nucleon knockout reactions induced by electron scattering are investigated. The nuclear structure functions are evaluated for nuclear matter. Realistic NN interactions derived in the framework of One-Boson-Exchange model are employed to evaluate the effects of correlations and MEC in a consistent way. The correlations correlations are determined by solving the Bethe-Goldstone equation. This yields significant contributions to the structure functions W_L and W_T of the (e,e'pn) and (e,e'pp) reactions. These contributions compete with MEC corrections originating from the $\pi$ and $\rho$ exchange terms of the same interaction. Special attention is paid to the so-called 'super parallel' kinematics at momentum transfers which can be measured e.g. at MAMI in Mainz.Comment: 14 pages, 8 figures include

Expression of yeast lipid phosphatase Sac1p is regulated by phosphatidylinositol-4-phosphate

<p>Abstract</p> <p>Background</p> <p>Phosphoinositides play a central role in regulating processes at intracellular membranes. In yeast, a large number of phospholipid biosynthetic enzymes use a common mechanism for transcriptional regulation. Yet, how the expression of genes encoding lipid kinases and phosphatases is regulated remains unknown.</p> <p>Results</p> <p>Here we show that the expression of lipid phosphatase Sac1p in the yeast <it>Saccharomyces cerevisiae </it>is regulated in response to changes in phosphatidylinositol-4-phosphate (PI(4)P) concentrations. Unlike genes encoding enzymes involved in phospholipid biosynthesis, expression of the <it>SAC1 </it>gene is independent of inositol levels. We identified a novel 9-bp motif within the 5' untranslated region (5'-UTR) of <it>SAC1 </it>that is responsible for PI(4)P-mediated regulation. Upregulation of <it>SAC1 </it>promoter activity correlates with elevated levels of Sac1 protein levels.</p> <p>Conclusion</p> <p>Regulation of Sac1p expression via the concentration of its major substrate PI(4)P ensures proper maintenance of compartment-specific pools of PI(4)P.</p

Local erythropoietin and endothelial progenitor cells improve regional cardiac function in acute myocardial infarction

<p>Abstract</p> <p>Background</p> <p>Expanded endothelial progenitor cells (eEPC) improve global left ventricular function in experimental myocardial infarction (MI). Erythropoietin beta (EPO) applied together with eEPC may improve regional myocardial function even further by anti-apoptotic and cardioprotective effects. Aim of this study was to evaluate intramyocardial application of eEPCs and EPO as compared to eEPCs or EPO alone in experimental MI.</p> <p>Methods and Results</p> <p>In vitro experiments revealed that EPO dosed-dependently decreased eEPC and leukocyte apoptosis. Moreover, in the presence of EPO mRNA expression in eEPC of proangiogenic and proinflammatory mediators measured by TaqMan PCR was enhanced. Experimental MI was induced by ligation and reperfusion of the left anterior descending coronary artery of nude rats (n = 8-9). After myocardial transplantation of eEPC and EPO CD68+ leukocyte count and vessel density were enhanced in the border zone of the infarct area. Moreover, apoptosis of transplanted CD31 + TUNEL + eEPC was decreased as compared to transplantation of eEPCs alone. Regional wall motion of the left ventricle was measured using Magnetic Resonance Imaging. After injection of eEPC in the presence of EPO regional wall motion significantly improved as compared to injection of eEPCs or EPO alone.</p> <p>Conclusion</p> <p>Intramyocardial transplantation of eEPC in the presence of EPO during experimental MI improves regional wall motion. This was associated with an increased local inflammation, vasculogenesis and survival of the transplanted cells. Local application of EPO in addition to cell therapy may prove beneficial in myocardial remodeling.</p