2,140 research outputs found
Ultra Luminous X-ray Sources: a deeper insight into their spectral evolution
We select a sample of nearby Ultraluminous X-ray sources with long XMM-Newton
observations and analyse all the available XMM-Newton data using both X-ray
spectral fitting techniques and hardness-intensity diagrams. The sample
includes IC 342 X-1, NGC 5204 X-1, NGC 5408 X-1, Holmberg IX X-1, Holmberg II
X-1, NGC 1313 X-1, NGC 1313 X-2 and NGC 253 X-1. We found that, although a
common reference model can be used to describe the X-ray spectra, the sources
show different spectral evolutions, phenomenologically described in terms of
variations in the properties of a soft component and a high energy tail.
Variations at low energies are accounted for (mostly) by changes in the
normalization of the soft component and/or in the column density to the source,
while variations in the high energy tail by changes in the parameters of an
optically thick corona. This spectral variability is rather well characterized
on a colour-colour and hardness-intensity diagram in terms of suitably defined
hardness ratios. We suggest the existence of a variability pattern on the
hardness-intensity diagram and we interpret it in terms of the switch between a
near-Eddington and a super-Eddington accretion regime. The transition between
the two regimes seems to be driven mostly by changes in the contribution of the
soft component, which can be explained in terms of the increasing importance of
wind emission. The analysis is complemented by an investigation of the
short-term time variability of all the sources. In general, no clear
correlation between the spectral and temporal properties is found.Comment: 15 pages, 7 figures, 5 tables. Accepted for publication in MNRA
Evidence for reduced magnetic braking in polars from binary population models
We present the first population synthesis of synchronous magnetic cataclysmic variables, called polars, taking into account the effect of the white dwarf (WD) magnetic field on angular momentum loss. We implemented the reduced magnetic braking (MB) model proposed by Li, Wu & Wickramasinghe into the Binary Stellar Evolution (BSE) code recently calibrated for cataclysmic variable (CV) evolution. We then compared separately our predictions for polars and non-magnetic CVs with a large and homogeneous sample of observed CVs from the Sloan Digital Sky Survey. We found that the predicted orbital period distributions and space densities agree with the observations if period bouncers are excluded. For polars, we also find agreement between predicted and observed mass transfer rates, while the mass transfer rates of non-magnetic CVs with periods âł3 h drastically disagree with those derived from observations. Our results provide strong evidence that the reduced MB model for the evolution of highly magnetized accreting WDs can explain the observed properties of polars. The remaining main issues in our understanding of CV evolution are the origin of the large number of highly magnetic WDs, the large scatter of the observed mass transfer rates for non-magnetic systems with periods âł3 h, and the absence of period bouncers in observed samples
Sustainable Panels with Recycled Materials for Building Applications: Environmental and Acoustic Characterizationâ
Abstract Sound absorption materials structure is generally based on porous synthetic media (rock wool, glass wool, polyurethane, polyester, ect.): they have expensive production processes, important energy consumptions, and high environmental impact. Recycled materials are becoming an interesting alternative, due to their good acoustic behavior, similar to traditional porous materials; they also allow low impact production costs, thanks to the use of wastes derived from other production cycles. This work focuses on the evaluation of the acoustic absorption properties of new panels made of recycled paper and other scrap materials, as wool and nonwoven polyester fabric: different samples were produced and tested by means of impedance tube, according to ISO 10534-2. In order to present the environmental benefits, Life Cycle Assessment was carried out in terms of primary embodied energy and greenhouse gas emissions, considering a "cradle-to-gate" approach. Furthermore, the behavior of innovative absorption materials was investigated in order to improve the acoustic performance of a lecture room, by means of an acoustic simulation software. A comparison with traditional materials was also carried out for both acoustic and environmental aspects. In the simulation model, calibrated by an in-situ experimental campaign of the main acoustic quality indexes (Reverberation Time, Clarity and Definition Indexes, Speech Transmission Index), different acoustic correction solutions were implemented: both the new recycled and traditional panels were applied as wall and ceiling absorbers. The analysis of the acoustic absorption trends, in 100 - 5000 Hz frequencies range, shows that the new materials are suitable as acoustic correction systems, especially the panel composed by waste paper and wool fibers. The LCA analysis results show that, considering the same acoustic performance, the recycled panels allow to reduce the environmental effects and the global production costs
The memory space: Exploring future uses of Web 2.0 and mobile internet through design interventions.
The QuVis Quantum Mechanics Visualization project aims to address challenges
of quantum mechanics instruction through the development of interactive
simulations for the learning and teaching of quantum mechanics. In this
article, we describe evaluation of simulations focusing on two-level systems
developed as part of the Institute of Physics Quantum Physics resources.
Simulations are research-based and have been iteratively refined using student
feedback in individual observation sessions and in-class trials. We give
evidence that these simulations are helping students learn quantum mechanics
concepts at both the introductory and advanced undergraduate level, and that
students perceive simulations to be beneficial to their learning.Comment: 15 pages, 5 figures, 1 table; accepted for publication in the
American Journal of Physic
Endothelin-1 Drives Epithelial-Mesenchymal Transition In Hypertensive Nephroangiosclerosis
BACKGROUND: Tubulointerstitial fibrosis, the final outcome of most kidney diseases, involves activation of epithelial mesenchymal transition (EMT). Endothelinâ1 (ETâ1) activates EMT in cancer cells, but it is not known whether it drives EMT in the kidney. We therefore tested the hypothesis that tubulointerstitial fibrosis involves EMT driven by ETâ1. METHODS AND RESULTS: Transgenic TG[mRen2]27 (TGRen2) rats developing fulminant angiotensin IIâdependent hypertension with prominent cardiovascular and renal damage were submitted to drug treatments targeted to ETâ1 and/or angiotensin II receptor or left untreated (controls). Expressional changes of Eâcadherin and αâsmooth muscle actin (αSMA) were examined as markers of renal EMT. In human kidney HKâ2 proximal tubular cells expressing the ET(B) receptor subtype, the effects of ETâ1 with or without ETâ1 antagonists were also investigated. The occurrence of renal fibrosis was associated with EMT in control TGRen2 rats, as evidenced by decreased Eâcadherin and increased αSMA expression. Irbesartan and the mixed ETâ1 receptor antagonist bosentan prevented these changes in a blood pressureâindependent fashion (P < 0.001 for both versus controls). In HKâ2 cells ETâ1 blunted Eâcadherin expression, increased αSMA expression (both P < 0.01), collagen synthesis, and metalloproteinase activity (P < 0.005, all versus untreated cells). All changes were prevented by the selective ET(B) receptor antagonist BQâ788. Evidence for involvement of the Rhoâkinase signaling pathway and dephosphorylation of Yesâassociated protein in EMT was also found. CONCLUSIONS: In angiotensin IIâdependent hypertension, ETâ1 acting via ET(B) receptors and the Rhoâkinase and Yesâassociated protein induces EMT and thereby renal fibrosis
Detection of Autoantibodies against Recombinant Desmoglein 1 and 3 Molecules in Patients with Pemphigus vulgaris: Correlation with Disease Extent at the Time of Diagnosis and during Follow-Up
The recent availability of cDNA clones for pemphigus antigens has allowed the production of recombinant desmoglein 1 and desmoglein 3 molecules and the development of an ELISA approach in order to determine levels of antibodies to them. The aim of the study was to determine the relationship between autoantibodies levels and the extent of both mucosal and skin lesions in 20 patients with pemphigus vulgaris at the time of diagnosis and during follow-up. For the detection of autoantibodies by ELISA we used the recombinant proteins expressing overlapping sequences with the entire extracellular desmoglein 1 and desmoglein 3 domains. We showed that in presence of mucosal lesions there was a correlation between extension of mucosal involvement and autoantiboidies titres against both desmoglein 1 and desmoglein 3, whereas in presence of skin lesions there was a statistically significant correlation between extension of skin lesions and autoantibodies titres against desmoglein 3, but not against desmoglein 1. A not negligible number of patients showed variations of the desmoglein 3 autoantibodies titre which did not correlate with the severity of both cutaneous and mucosal involvement. Similar results were obtained analyzing autoantibodies titres against desmoglein 1. In conclusion, we believe that the utilization of recombinant desmoglein 1 and desmoglein 3 proteins by ELISA should be used with caution to monitor disease severity and response to therapy, although it remains a high specific test for the initial diagnosis of pemphigus and the identification of a change in the clinical phenotype of this condition
The Importance of Reading the Skin: Cutaneous Metastases of Pancreatic Cancer, a Systematic Review
Background: Pancreatic cancer is notorious for its aggressive nature and low survival rate, with less than 10% of patients surviving beyond five years. Early detection is difficult, but skin metastases can be a rare but significant indicator. This systematic review focuses on the epidemiology, clinical features, and histology of skin metastases from pancreatic cancer to determine their importance in early diagnosis and overall management of the disease. Materials and methods: Following PRISMA guidelines, we conducted an exhaustive search of MEDLINE/PubMed, EMBASE, and SCOPUS databases up to June 2023, using specific keywords. Four independent investigators screened the studies using predefined criteria, and two investigators checked the accuracy and consistency of the data extraction. We assessed the quality of the trials using adapted criteria from the Joanna Briggs Institute. A narrative synthesis rather than a meta-analysis was chosen because of the different study designs. Results: The final analysis included 57 patients with skin metastases from pancreatic cancer. Cutaneous metastases, although rare, presented with approximately equal gender distribution and a mean age of 63.4 years. Predominantly non-umbilical (77%), these metastases showed clinical diversity, ranging from asymptomatic nodules to painful or ulcerated lesions. Notably, skin metastases often preceded the diagnosis of primary pancreatic cancer (58%). Primary tumor characteristics revealed different localizations, with adenocarcinoma being the most prevalent histological type (77%). A significant association (p = 0.008) was observed between pancreatic tumor location and the timing of presentation of skin metastases. Tumors located in the body and tail of the pancreas were more likely to manifest skin metastases as an initial clinical manifestation (62.2%) than those in the head of the pancreas (20.8%). Conclusions: In conclusion, although skin metastases are rare, they are important indicators of pancreatic cancer, highlighting the need for multidisciplinary healthcare collaboration and thorough skin examination. Recognizing them could lead to earlier diagnosis, which is crucial in a cancer with limited treatment options
The Dynamic Cell The roles of the oncoprotein GOLPH3 in contractile ring assembly and membrane trafficking during cytokinesis
Abstract Cytokinesis is an intricate process that requires an intimate interplay between actomyosin ring constriction and plasma membrane remodelling at the cleavage furrow. However, the molecular mechanisms involved in coupling the cytoskeleton dynamics with vesicle trafficking during cytokinesis are poorly understood. The highly conserved Golgi phosphoprotein 3 (GOLPH3), functions as a phosphatidylinositol 4-phosphate (PI4P) effector at the Golgi. Recent studies have suggested that GOLPH3 is up-regulated in several cancers and is associated with poor prognosis and more aggressive tumours. In Drosophila melanogaster, GOLPH3 localizes at the cleavage furrow of dividing cells, is required for successful cytokinesis and acts as a key molecule in coupling phosphoinositide (PI) signalling with actomyosin ring dynamics. Because cytokinesis failures have been linked with pre-malignant disease and cancer, the novel connection between GOLPH3 and cytokinesis imposes new fields of investigation in cancer biology and therapy
Expression and Functional Role of Urotensin-II and Its Receptor in the Adrenal Cortex and Medulla: Novel Insights for the Pathophysiology of Primary Aldosteronism
Abstract
Context: The involvement of urotensin II, a vasoactive peptide acting via the G protein-coupled urotensin II receptor, in arterial hypertension remains contentious.
Objective: We investigated the expression of urotensin II and urotensin II receptor in adrenocortical and adrenomedullary tumors and the functional effects of urotensin II receptor activation.
Design: The expression of urotensin II and urotensin II receptor was measured by real time RT-PCR in aldosterone-producing adenoma (n = 22) and pheochromocytoma (n = 10), using histologically normal adrenocortical (n = 6) and normal adrenomedullary (n = 5) tissue as control. Urotensin II peptide and urotensin II receptor protein were investigated with immunohistochemistry and immunoblotting. To identify urotensin II-related and urotensin II receptor-related pathways, a whole transcriptome analysis was used. The adrenocortical effects of urotensin II receptor activation were also assessed by urotensin II infusion with/without the urotensin II receptor antagonist palosuran in rats.
Results: Urotensin II was more expressed in pheochromocytoma than in aldosterone-producing adenoma tissue; the opposite was seen for the urotensin II receptor expression. Urotensin II receptor activation in vivo in rats enhanced (by 182 ± 9%; P < 0.007) the adrenocortical expression of immunoreactive aldosterone synthase.
Conclusions: Urotensin II is a putative mediator of the effects of the adrenal medulla and pheochromocytoma on the adrenocortical zona glomerulosa. This pathophysiological link might account for the reported causal relationship between pheochromocytoma and primary aldosteronism
Rab1 interacts with GOLPH3 and controls Golgi structure and contractile ring constriction during cytokinesis in Drosophila melanogaster
Cytokinesis requires a tight coordination between actomyosin ring constriction and new membrane addition along the ingressing cleavage furrow. However, the molecular mechanisms underlying vesicle trafficking to the equatorial site and how this process is coupled with the dynamics of the contractile apparatus are poorly defined. Here we provide evidence for the requirement of Rab1 during cleavage furrow ingression in cytokinesis. We demonstrate that the gene omelette (omt) encodes the Drosophila orthologue of human Rab1 and is required for successful cytokinesis in both mitotic and meiotic dividing cells of Drosophila melanogaster. We show that Rab1 protein colocalizes with the conserved oligomeric Golgi (COG) complex Cog7 subunit and the phosphatidylinositol 4-phosphate effector GOLPH3 at the Golgi stacks. Analysis by transmission electron microscopy and 3D-SIM super-resolution microscopy reveals loss of normal Golgi architecture in omt mutant spermatocytes indicating a role for Rab1 in Golgi formation. In dividing cells, Rab1 enables stabilization and contraction of actomyosin rings. We further demonstrate that GTP-bound Rab1 directly interacts with GOLPH3 and controls its localization at the Golgi and at the cleavage site. We propose that Rab1, by associating with GOLPH3, controls membrane trafficking and contractile ring constriction during cytokinesis
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