An accretion-jet model for M87: interpreting the spectral energy distribution and Faraday rotation measure

M87 is arguably the best supermassive black hole (BH) to explore the jet and/or accretion physics due to its proximity and fruitful high-resolution multi-waveband observations. We model the multi-wavelength spectral energy distribution (SED) of M87 core that observed at a scale of 0.4 arcsec ($\sim 10^5R_{\rm g}$, $R_{\rm g}$ is gravitational radius) as recently presented by Prieto et al. Similar to Sgr A*, we find that the millimeter bump as observed by Atacama Large Millimeter/submillimeter Array (ALMA) can be modeled by the synchrotron emission of the thermal electrons in advection dominated accretion flow (ADAF), while the low-frequency radio emission and X-ray emission may dominantly come from the jet. The millimeter radiation from ADAF dominantly come from the region within $10R_{\rm g}$, which is roughly consistent with the recent very long baseline interferometry observations at 230\,GHz. We further calculate the Faraday rotation measure (RM) from both ADAF and jet models, and find that the RM predicted from the ADAF is roughly consistent with the measured value while the RM predicted from the jet is much higher if jet velocity close to the BH is low or moderate (e.g., $v_{\rm jet}\lesssim0.6\,c$). With the constraints from the SED modeling and RM, we find that the accretion rate close to the BH horizon is $\sim (0.2-1)\times10^{-3}{M}_{\odot} \rm yr^{-1}\ll\dot{\it M}_{\rm B}\sim 0.2\it {M}_{\odot} \rm yr^{-1}$ ($\dot{M}_{\rm B}$ is Bondi accretion rate), where the electron density profile, $n_{\rm e}\propto r^{\sim -1}$, in the accretion flow is consistent with that determined from X-ray observation inside the Bondi radius and recent numerical simulations.Comment: 8 pages, 3 figures, accepted for publication in Ap

Induction of colonic epithelial cell apoptosis by p47-dependent oxidants11Nucleotide sequence data reported are available in GenBank database under accession # AF540955.

AbstractExogenous oxidants appear capable of initiating both proliferative and death signals, but the role of endogenous oxidants in either tumorigenesis or tumor suppression is unclear. We found that expression of the NAD(P)H oxidase adapter p47phox was suppressed in human colon carcinoma specimens relative to adjacent normal colon. Overexpression of p47phox increased apoptosis in colon cancer cell lines independent of p53 and mismatch-repair competency. p47phox was found to interact with the c-Abl adapter Abl interactor-1 (ABI-1), and p47phox coprecipitated with both ABI-1 and c-Abl. Ectopic expression of p47phox in colon cancer cells increased oxidant production with phosphorylation and activation of nuclear c-Abl and consequent apoptosis. Colonic epithelial p47phox may be specifically targeted to a c-Abl-containing complex that serves a physiologic tumor suppressing function

Testing and Data Reduction of the Chinese Small Telescope Array (CSTAR) for Dome A, Antarctica

The Chinese Small Telescope ARray (hereinafter CSTAR) is the first Chinese astronomical instrument on the Antarctic ice cap. The low temperature and low pressure testing of the data acquisition system was carried out in a laboratory refrigerator and on the 4500m Pamirs high plateau, respectively. The results from the final four nights of test observations demonstrated that CSTAR was ready for operation at Dome A, Antarctica. In this paper we present a description of CSTAR and the performance derived from the test observations.Comment: Accepted Research in Astronomy and Astrophysics (RAA) 1 Latex file and 20 figure

Subcellular targeting of oxidants during endothelial cell migration

Endogenous oxidants participate in endothelial cell migration, suggesting that the enzymatic source of oxidants, like other proteins controlling cell migration, requires precise subcellular localization for spatial confinement of signaling effects. We found that the nicotinamide adenine dinucleotide phosphate reduced (NADPH) oxidase adaptor p47phox and its binding partner TRAF4 were sequestered within nascent, focal complexlike structures in the lamellae of motile endothelial cells. TRAF4 directly associated with the focal contact scaffold Hic-5, and the knockdown of either protein, disruption of the complex, or oxidant scavenging blocked cell migration. An active mutant of TRAF4 activated the NADPH oxidase downstream of the Rho GTPases and p21-activated kinase 1 (PAK1) and oxidatively modified the focal contact phosphatase PTP-PEST. The oxidase also functioned upstream of Rac1 activation, suggesting its participation in a positive feedback loop. Active TRAF4 initiated robust membrane ruffling through Rac1, PAK1, and the oxidase, whereas the knockdown of PTP-PEST increased ruffling independent of oxidase activation. Our data suggest that TRAF4 specifies a molecular address within focal complexes that is targeted for oxidative modification during cell migration

Assessment of latent tuberculosis infection in psychiatric inpatients: A survey after tuberculosis outbreaks

AbstractBackground/PurposeTo investigate risk factors of latent tuberculosis infection (LTBI) among inpatients of chronic psychiatric wards with tuberculosis (TB) outbreaks.MethodsIn April 2013, inpatients of four all-male wards with TB outbreaks were tested for LTBI using the QuantiFERON-TB Gold in Tube (QFT) method. Based on this investigation, a retrospective study was conducted to assess risk factors for LTBI. Inpatients exposed to cluster-A or cluster-B TB cases were defined as contacts of cluster-A or cluster-B, and others, as nonclustered contacts.ResultsAmong 355 inpatients with TB exposure, 134 (38%) were QFT-positive for LTBI. Univariate analysis showed that significant predictors for QFT-positivity were age, case-days of exposure to all TB cases (TB-all) and to sputum smear positive cases, number of source cases with cough, and exposure to cluster-A TB cases. Independent risk factors for LTBI were higher age [adjusted odds ratio (OR) 1.03, 95% confidence intervals (CI: 1.01–1.05)], TB-all exposure case-days ≥ 200 [adjusted OR 2.04 (1.06–3.92)] and exposure to cluster-A TB cases [adjusted OR 2.82 (1.30–6.12)] after adjustment for the sputum smear positivity, and cough variables of the source cases. The contacts of cluster-A had a greater risk of LTBI than did those of cluster-B, especially in the younger population (≤50 years) after adjustment [adjusted OR 2.64 (1.03–6.76)].ConclusionAfter TB outbreaks, more than one third of inpatients were QFT-positive for LTBI. Our findings suggest that, beside the infectiousness of source cases, intensity of exposure, and age of contacts, exposure to TB cases in potential genotyping clusters may be predictive for LTBI in this male psychiatric population

Nitrato(1,10-phenanthroline)(1H-1,2,4-triazole-3-carboxyl­ato)copper(II)

In the title complex, [Cu(C3H2N3O2)(NO3)(C12H8N2)], the CuII ion is coordinated by an N and an O atom from a bidentate 1H-1,2,4-triazole-3-carboxyl­ate (TRIA) ligand, two N atoms from a 1,10-phenanthroline (phen) ligand, and an O atom from a nitrate ligand in a slightly distorted square-pyramidal environment. In the crystal structure, inter­molecular N—H⋯O hydrogen bonds link mol­ecules into one-dimensional chains propagating along the b axis direction

Genomic sequencing and analyses of Lymantria xylina multiple nucleopolyhedrovirus

<p>Abstract</p> <p>Background</p> <p>Outbreaks of the casuarina moth, <it>Lymantria xylina </it>Swinehoe (Lepidoptera: Lymantriidae), which is a very important forest pest in Taiwan, have occurred every five to 10 years. This moth has expanded its range of host plants to include more than 65 species of broadleaf trees. LyxyMNPV (<it>L. xylina </it>multiple nucleopolyhedrovirus) is highly virulent to the casuarina moth and has been investigated as a possible biopesticide for controlling this moth. LdMNPV-like virus has also been isolated from <it>Lymantria xylin</it>a larvae but LyxyMNPV was more virulent than LdMNPV-like virus both in NTU-LY and IPLB-LD-652Y cell lines. To better understand LyxyMNPV, the nucleotide sequence of the LyxyMNPV DNA genome was determined and analysed.</p> <p>Results</p> <p>The genome of LyxyMNPV consists of 156,344 bases, has a G+C content of 53.4% and contains 157 putative open reading frames (ORFs). The gene content and gene order of LyxyMNPV were similar to those of LdMNPV, with 151 ORFs identified as homologous to those reported in the LdMNPV genome. Two genes (Lyxy49 and Lyxy123) were homologous to other baculoviruses, and four unique LyxyMNPV ORFs (Lyxy11, Lyxy19, Lyxy130 and Lyxy131) were identified in the LyxyMNPV genome, including a <it>gag-like </it>gene that was not reported in baculoviruses. LdMNPV contains 23 ORFs that are absent in LyxyMNPV. Readily identifiable homologues of the gene <it>host range factor-1 </it>(<it>hrf-1</it>), which appears to be involved in the susceptibility of <it>L. dispar </it>to NPV infection, were not present in LyxyMNPV. Additionally, two putative <it>odv-e27 </it>homologues were identified in LyxyMNPV. The LyxyMNPV genome encoded 14 <it>bro </it>genes compared with 16 in LdMNPV, which occupied more than 8% of the LyxyMNPV genome. Thirteen homologous regions (<it>hr</it>s) were identified containing 48 repeated sequences composed of 30-bp imperfect palindromes. However, they differed in the relative positions, number of repeats and orientation in the genome compared to LdMNPV.</p> <p>Conclusion</p> <p>The gene parity plot analysis, percent identity of the gene homologues and a phylogenetic analysis suggested that LyxyMNPV is a Group II NPV that is most closely related to LdMNPV but with a highly distinct genomic organisation.</p

Cellular basis of urothelial squamous metaplasia: roles of lineage heterogeneity and cell replacement

Although the epithelial lining of much of the mammalian urinary tract is known simply as the urothelium, this epithelium can be divided into at least three lineages of renal pelvis/ureter, bladder/trigone, and proximal urethra based on their embryonic origin, uroplakin content, keratin expression pattern, in vitro growth potential, and propensity to keratinize during vitamin A deficiency. Moreover, these cells remain phenotypically distinct even after they have been serially passaged under identical culture conditions, thus ruling out local mesenchymal influence as the sole cause of their in vivo differences. During vitamin A deficiency, mouse urothelium form multiple keratinized foci in proximal urethra probably originating from scattered K14-positive basal cells, and the keratinized epithelium expands horizontally to replace the surrounding normal urothelium. These data suggest that the urothelium consists of multiple cell lineages, that trigone urothelium is closely related to the urothelium covering the rest of the bladder, and that lineage heterogeneity coupled with cell migration/replacement form the cellular basis for urothelial squamous metaplasia