Non-steller light from high-redshift radiogalaxies

With the aid of a new IRCAM image of 3C356, researchers question the common assumption that radiosource-stimulated starbursts are responsible for the extended optical emission aligned with radio structures in high-redshift radiogalaxies. They propose an alternative model in which the radiation from a hidden luminous quasar is beamed along the radio axis and illuminates dense clumps of cool gas to produce both extended narrow emission line regions and, by Thomson scattering, extended optical continua. Simple observational tests of this model are possible and necessary if we are to continue to accept that the color, magnitude and shape evolution of radiogalaxies are controlled by the active evolution of stellar populations

The Linear-Size Evolution of Classical Double Radio Sources

Recent investigations of how the median size of extragalactic radio sources change with redshift have produced inconsistent results. Eales compared the radio and optical properties of a bright 3C and faint 6C sample and concluded that $D\propto(1+z)^{-1.1\pm0.5}$ ($\Omega_0 = 0$), with $D$ being the median size of the radio sources at a given epoch and z the redshift. Oort, Katgert, and Windhorst, on the other hand, from a comparison of the properties of a number of radio samples, found much stronger evolution, with $D\propto(1+z)^{-3.3 \pm0.5}$. In this paper we attempt to resolve the difference. We have repeated the analysis of Eales using the virtually complete redshift information that now exists for the 6C sample. Confining our analysis to FR2 sources, which we argue is the best-understood class of radio sources and the least likely to be affected by selection effects, we find $D\propto(1+z)^{-1.2\pm0.5}$ ($\Omega_0 = 0$) and $D\propto(1+z)^{-1.7\pm0.4}$ ($\Omega_0 = 1$). Our complete redshift information allows us to gain insight into our result by plotting a radio luminosity-size (P-D) diagram for the 6C sample. The most obvious difference between the 3C and 6C P-D diagrams is the clump of sources in the 6C diagram at $D\sim 100 kpc, P_{151}\sim 5x10^{27} WHz^{-1}sr^{-1}$. These clump sources have similar sizes to the emission-line regions found around high-redshift radio galaxies, suggesting that the presence of dense line-emitting gas around high-redshift radio galaxies is responsible for the size evolution. We show that this explanation can quantitatively explain the observed size evolution, as long as there is either little X-ray emitting gas around these objects or, if there is, it is distributed in a similar way to the emission-line gas: highly anisotropic and inhomogeneous.Comment: compressed and uuencoded postscript file. 33 pages including 5 figures (441951 bytes). Accepted for publication in September Ap

The radio luminosity function from the low-frequency 3CRR, 6CE & 7CRS complete samples

We measure the radio luminosity function (RLF) of steep-spectrum radio sources using three redshift surveys of flux-limited samples selected at low (151 & 178 MHz) radio frequency, low-frequency source counts and the local RLF. The redshift surveys used are the new 7C Redshift Survey (7CRS) and the brighter 3CRR and 6CE surveys totalling 356 sources with virtually complete redshift information. This yields unprecedented coverage of the radio luminosity versus z plane for steep-spectrum sources, and hence the most accurate measurements of the steep-spectrum RLF yet made. We find that a simple dual-population model for the RLF fits the data well, requiring differential density evolution (with z) for the two populations. The low-luminosity population can be associated with radio galaxies with weak emission lines, and includes sources with both FRI and FRII radio structures; its comoving space density $\rho$ rises by about one dex between z~0 and z~1 but cannot yet be meaningfully constrained at higher redshifts. The high-luminosity population can be associated with FRII radio galaxies and quasars with strong emission lines; its $\rho$ rises by nearly three dex between z~0 and z~2. These results mirror the situation seen in X-ray and optically-selected AGN. The integrated radio luminosity density of the combination of the two populations is controlled by the value of $\rho$ at the low-luminosity end of the RLF of the high-luminosity population, a quantity which has been directly measured at z~1 by the 7CRS. We argue that robust determination of this quantity at higher redshifts requires a new redshift survey based on a large (~1000 source) sample about five times fainter than the 7CRS.Comment: 20 pages, 16 figures, accepted for publication in MNRA

A sample of 6C radio sources designed to find objects at redshift > 4: the radio data

We describe the selection of a sample of 34 radio sources from the 6C survey (Hales, Baldwin & Warner 1993) from a region of sky covering 0.133 sr. The selection criteria for this sample, hereafter called 6C*, were chosen to optimise the chances of finding radio galaxies at redshift z > 4. Optical follow-up observations have already led to the discovery of the most distant known radio galaxy at z = 4.41 (Rawlings et al. 1996). We present VLA radio maps and derive radio spectra for all the 6C* objects.Comment: 18 pages, LaTeX; also available at http://www-astro.physics.ox.ac.uk/research/preprints/ To appear in MNRA

Using Interleukin 6 and 8 in Blood and Bronchoalveolar Lavage Fluid to Predict Survival in Hematological Malignancy Patients With Suspected Pulmonary Mold Infection.

Background: Molds and other pathogens induce elevated levels of several cytokines, including interleukin (IL)-6 and IL-8. The objective of this study was to investigate the prognostic value of IL-6 and IL-8 as well as fungal biomarkers in blood and bronchoalveolar lavage fluid (BAL) for overall survival in patients with underlying hematological malignancies and suspected mold infection. Methods: This cohort study included 106 prospectively enrolled adult cases undergoing bronchoscopy. Blood samples were collected within 24 h of BAL sampling and, in a subset of 62 patients, serial blood samples were collected up until 4 days after bronchoscopy. IL-6, IL-8, and other cytokines as well as galactomannan (GM) and β-D-glucan (BDG) were assayed in blood and BAL fluid and associations with overall mortality were assessed at the end of the study using receiver operating characteristic (ROC) curve analysis. Results: Both blood IL-8 (AUC 0.731) and blood IL-6 (AUC 0.699) as well as BAL IL-6 (AUC 0.763) and BAL IL-8 (AUC 0.700) levels at the time of bronchoscopy were predictors of 30-day all-cause mortality. Increasing blood IL-6 levels between bronchoscopy and day four after bronchoscopy were significantly associated with higher 90-day mortality, with similar findings for increasing IL-8 levels. In ROC analysis the difference of blood IL-8 levels between 4 days after bronchoscopy and the day of bronchoscopy had an AUC of 0.829 (95%CI 0.71-0.95; p < 0.001) for predicting 90-day mortality. Conclusions: Elevated levels of IL-6 and IL-8 in blood or BAL fluid at the time of bronchoscopy, and rising levels in blood 4 days following bronchoscopy were predictive of mortality in these patients with underlying hematological malignancy who underwent bronchoscopy for suspected mold infection

Perturbation of the P-Body Component Mov10 Inhibits HIV-1 Infectivity

Exogenous retroviruses are obligate cellular parasites that co-opt a number of host proteins and functions to enable their replication and spread. Several host factors that restrict HIV and other retroviral infections have also recently been described. Here we demonstrate that Mov10, a protein associated with P-bodies that has a putative RNA-helicase domain, when overexpressed in cells can inhibit the production of infectious retroviruses. Interestingly, reducing the endogenous Mov10 levels in virus-producing cells through siRNA treatment also modestly suppresses HIV infectivity. The actions of Mov10 are not limited to HIV, however, as ectopic expression of Mov10 restricts the production of other lentiviruses as well as the gammaretrovirus, murine leukemia virus. We found that HIV produced in the presence of high levels of Mov10 is restricted at the pre-reverse transcription stage in target cells. Finally, we show that either helicase mutation or truncation of the C-terminal half of Mov10, where a putative RNA-helicase domain is located, maintained most of its HIV inhibition; whereas removing the N-terminal half of Mov10 completely abolished its activity on HIV. Together these results suggest that Mov10 could be required during the lentiviral lifecycle and that its perturbation disrupts generation of infectious viral particles. Because Mov10 is implicated as part of the P-body complex, these findings point to the potential role of cytoplasmic RNA processing machinery in infectious retroviral production

Protein tyrosine phosphatase PTPN22 regulates LFA-1 dependent Th1 responses

A missense C1858T single nucleotide polymorphism within PTPN22 is a strong genetic risk factor for the development of multiple autoimmune diseases. PTPN22 encodes a protein tyrosine phosphatase that negatively regulates immuno-receptor proximal Src and Syk family kinases. Notably, PTPN22 negatively regulates kinases downstream of T-cell receptor (TCR) and LFA-1, thereby setting thresholds for T-cell activation. Alterations to the quality of TCR and LFA-1 engagement at the immune synapse and the regulation of downstream signals can have profound effects on the type of effector T-cell response induced. Here we describe how IFNγ+ Th1 responses are potentiated in Ptpn22−/− T-cells and in T-cells from mice expressing Ptpn22R619W (the mouse orthologue of the human genetic variant) as they age, or following repeated immune challenge, and explore the mechanisms contributing to the expansion of Th1 cells. Specifically, we uncover two LFA-1-ICAM dependent mechanisms; one T-cell intrinsic, and one T-cell extrinsic. Firstly, we found that in vitro anti-CD3/LFA-1 induced Th1 responses were enhanced in Ptpn22−/− T-cells compared to WT, whereas anti-CD3/anti-CD28 induced IFNy responses were similar. These data were associated with an enhanced ability of Ptpn22−/− T-cells to engage ICAM-1 at the immune synapse when incubated on planar lipid bilayers, and to form conjugates with dendritic cells. Secondly, we observed a T-cell extrinsic mechanism whereby repeated stimulation of WT OT-II T-cells with LPS and OVA323-339 pulsed Ptpn22−/− bone marrow derived dendritic cells (BMDCs) was sufficient to enhance Th1 cell development compared to WT BMDCs. Furthermore, this response could be reversed by LFA-1 blockade. Our data point to two related but distinct mechanisms by which PTPN22 regulates LFA-1 dependent signals to enhance Th1 development, highlighting how perturbations to PTPN22 function over time to regulate the balance of the immune response

Classifying organisms and artefacts by their outline shapes

We often wish to classify objects by their shapes. Indeed, the study of shapes is an important part of many scientific fields, such as evolutionary biology, structural biology, image processing and archaeology. However, mathematical shape spaces are rather complicated and nonlinear. The most widely used methods of shape analysis, geometric morphometrics, treat the shapes as sets of points. Diffeomorphic methods consider the underlying curve rather than points, but have rarely been applied to real-world problems. Using a machine classifier, we tested the ability of several of these methods to describe and classify the shapes of a variety of organic and man-made objects. We find that one method, based on square-root velocity functions (SRVFs), outperforms all others, including a standard geometric morphometric method (eigenshapes), and that it is also superior to human experts using shape alone. When the SRVF approach is constrained to take account of homologous landmarks it can accurately classify objects of very different shapes. The SRVF method identifies a shortest path between shapes, and we show that this can be used to estimate the shapes of intermediate steps in evolutionary series. Diffeomorphic shape analysis methods, we conclude, now provide practical and effective solutions to many shape description and classification problems in the natural and human sciences.</p

Randomized controlled trial comparing three different modalities of lithotrites for intracorporeal lithotripsy in pcnl

Purpose: To compare the efficiency (stone fragmentation and removal time) and complications of three models of intracorporeal lithotripters in percutaneous nephrolithotomy (PCNL). Materials and Methods: Prospective, randomized controlled trial at nine centers in the North America from 2009 to 2016. Patients were randomized to one of three lithotripter devices: the Cyberwand, a dual probe ultrasonic device; the Swiss Lithoclast Select, a combination pneumatic and ultrasonic device; and the StoneBreaker, a portable pneumatic device powered by CO2 cartridges. Since the StoneBreaker lacks an ultrasonic component, it was used with the LUS‐II ultrasonic lithotripter to allow fair comparison with combination devices. Results: 270 patients were enrolled, 69 were excluded after randomization. 201 patients completed the study: 71 in the Cyberwand group, 66 in the Lithoclast Select, and 64 in the StoneBreaker group. The baseline patient characteristics of the three groups were similar. Mean stone surface area was smaller in the StoneBreaker group at 407.8mm2 vs 577.5mm2 (Lithoclast Select) and 627.9mm2 (Cyberwand). The stone clearance rate was slowest in the StoneBreaker group at 24.0 mm2/min vs 28.9 mm2/min and 32.3 mm2/min in the Lithoclast Select and Cyberwand groups respectively. After statistically adjusting for the smaller mean stone size in the StoneBreaker group, there was no difference in the stone clearance rate among the three groups (p=0.249). Secondary outcomes, including complications and stone free rates, were similar between the groups. Conclusions: The Cyberwand, Lithoclast Select, and the StoneBreaker lithotripters have similar adjusted stone clearance rates in PCNL for stones > 2cm. The safety and efficacy of these devices are comparable

Expression Analysis of PAC1-R and PACAP Genes in Zebrafish Embryos

This study describes the expression of the pituitary adenylate cyclase-activating polypeptide (PACAP1 and PACAP2) and PAC1 receptor genes (PAC1a-R and PAC1b-R) in the brain of zebrafish (Danio rerio) during development. In situ hybridization of the 24- and 48-hpf embryos revealed that PACAP genes were expressed in the telencephalon, the diencephalon, the rhombencephalon, and the neurons in the dorsal part of the spinal cord. PACAP2 mRNA appears to be the most abundant form during brain development. The two PAC1-R subtypes showed a similar expression pattern: mRNAs were detected in the forebrain, the thalamus, and the rhombencephalon. However, in the tectum, only PAC1b-R gene was detected. These results suggest that, in fish, PACAP may play a role in brain development