Phase diagram at finite temperature and quark density in the strong coupling limit of lattice QCD for color SU(3)

We study the phase diagram of quark matter at finite temperature (T) and finite chemical potential (mu) in the strong coupling limit of lattice QCD for color SU(3). We derive an analytical expression of the effective free energy as a function of T and mu, including baryon effects. The finite temperature effects are evaluated by integrating over the temporal link variable exactly in the Polyakov gauge with anti-periodic boundary condition for fermions. The obtained phase diagram shows the first order phase transition at low temperatures and the second order phase transition at high temperatures separated by the tri-critical point in the chiral limit. Baryon has effects to reduce the effective free energy and to extend the hadron phase to a larger mu direction at low temperatures.Comment: 18 pages, 10 figure

MarvelD3 regulates the c-Jun N-terminal kinase pathway during eye development in Xenopus.

Ocular morphogenesis requires several signalling pathways controlling the expression of transcription factors and cell-cycle regulators. However, despite a well-known mechanism, the dialogue between those signals and factors remains to be unveiled. Here, we identify a requirement for MarvelD3, a tight junction transmembrane protein, in eye morphogenesis in Xenopus MarvelD3 depletion led to an abnormally pigmented eye or even an eye-less phenotype, which was rescued by ectopic MarvelD3 expression. Altering MarvelD3 expression led to deregulated expression of cell-cycle regulators and transcription factors required for eye development. The eye phenotype was rescued by increased c-Jun terminal Kinase activation. Thus, MarvelD3 links tight junctions and modulation of the JNK pathway to eye morphogenesis

PRELP secreted from mural cells protects the function of blood brain barrier through regulation of endothelial cell-cell integrity

INTRODUCTION: Proline/arginine-rich end leucine-rich repeat protein (PRELP), is a small secreted proteoglycan expressed by pericytes and vascular smooth muscle cells surrounding the brain vasculature of adult mouse. METHODS: We utilised a Prelp knockout (Prelp−/−) mouse model to interrogate vasculature integrity in the brain alongside performing in vitro assays to characterise PRELP application to endothelial cells lines. Our findings were supplemented with RNA expression profiling to elucidate the mechanism of how PRELP maintains neurovasculature function. RESULTS: Prelp−/− mice presented with neuroinflammation and reducedneurovasculature integrity, resulting in IgG and dextran leakage in the cerebellum and cortex. Histological analysis of Prelp−/− mice revealed reducedcell-cell integrity of the blood brain barrier, capillary attachment of pericytes andastrocyte end-feet. RNA-sequencing analysis found that cell-cell adhesion andinflammation are affected in Prelp−/− mice and gene ontology analysis as well as gene set enrichment analysis demonstrated that inflammation related processes and adhesion related processes such as epithelial-mesenchymal transition and apical junctions were significantly affected, suggesting PRELP is a regulator of cell-cell adhesion. Immunofluorescence analysis showed that adhesion junction protein expression levels of cadherin, claudin-5, and ZO-1, was suppressed in Prelp−/− mice neurovasculature. Additionally, in vitro studies revealed that PRELP application to endothelial cells enhances cell-cell integrity, induces mesenchymal-endothelial transition and inhibits TGF-β mediated damage to cell-cell adhesion. DISCUSSION: Our study indicates that PRELP is a novel endogenous secreted regulator of neurovasculature integrity and that PRELP application may be a potential treatment for diseases associated with neurovascular damage

Prominin-1 Modulates Rho/ROCK-Mediated Membrane Morphology and Calcium-Dependent Intracellular Chloride Flux

Membrane morphology is an important structural determinant as it reflects cellular functions. The pentaspan membrane protein Prominin-1 (Prom1/CD133) is known to be localised to protrusions and plays a pivotal role in migration and the determination of cellular morphology; however, the underlying mechanism of its action have been elusive. Here, we performed molecular characterisation of Prom1, focussing primarily on its effects on cell morphology. Overexpression of Prom1 in RPE-1 cells triggers multiple, long, cholesterol-enriched fibres, independently of actin and microtubule polymerisation. A five amino acid stretch located at the carboxyl cytosolic region is essential for fibre formation. The small GTPase Rho and its downstream Rho-associated coiled-coil-containing protein kinase (ROCK) are also essential for this process, and active Rho colocalises with Prom1 at the site of initialisation of fibre formation. In mouse embryonic fibroblast (MEF) cells we show that Prom1 is required for chloride ion efflux induced by calcium ion uptake, and demonstrate that fibre formation is closely associated with chloride efflux activity. Collectively, these findings suggest that Prom1 affects cell morphology and contributes to chloride conductance

Cosmogenic 11C production and sensitivity of organic scintillator detectors to pep and CNO neutrinos

Several possible background sources determine the detectability of pep and CNO solar neutrinos in organic liquid scintillator detectors. Among such sources, the cosmogenic 11C nuclide plays a central role. 11C is produced underground in reactions induced by the residual cosmic muon flux. Experimental data available for the effective cross section for 11C by muons indicate that 11C will be the dominant source of background for the observation of pep and CNO neutrinos. 11C decays are expected to total a rate 2.5 (20) times higher than the combined rate of pep and CNO neutrinos in Borexino (KamLAND) in the energy window preferred for the pep measurement, between 0.8 and 1.3 MeV. This study examines the production mechanism of 11C by muon-induced showers in organic liquid scintillators with a novel approach: for the first time, we perform a detailed ab initio calculation of the production of a cosmogenic nuclide, 11C, taking into consideration all relevant production channels. Results of the calculation are compared with the effective cross sections measured by target experiments in muon beams. This paper also discusses a technique for reduction of background from 11C in organic liquid scintillator detectors, which allows to identify on a one-by-one basis and remove from the data set a large fraction of 11C decays. The background reduction technique hinges on an idea proposed by Martin Deutsch, who suggested that a neutron must be ejected in every interaction producing a 11C nuclide from 12C. 11C events are tagged by a three-fold coincidence with the parent muon track and the subsequent neutron capture on protons.Comment: 11 pages, 6 figures; added one section detailing comparison with previous estimates; added reference