INTEGRAL observation of the high-mass X-ray transient V 0332+53 during the 2005 outburst decline

The decline of the high mass X-ray transient V 0332+53 during the Dec. 2004 to Feb. 2005 outburst is analysed from the data recorded by INTEGRAL. The flux is shown to decrease exponentially until 2005 Feb. 10, with a decay time scale of ∼30 days above 20 keV and ∼20 days at lower energies, and to decrease linearly thereafter. The energy spectrum is well modelled throughout the decay by a power law with a folding energy of ∼7.5 keV, and with two cyclotron absorption features. The folding energy does not vary significantly over the decay, but the spectrum becomes harder with time. Most importantly, we show that the parameters describing the fundamental cyclotron line around 27 keV do vary with time: its energy and depth increase (by about 17% for the energy in ∼6 weeks), while its width decreases. These changes of the cyclotron line parameters are interpreted as resulting from a change in the extent of the cyclotron scattering region. Two quasi-periodic oscillations are also observed at various times during the observations, one at 0.05 Hz and another one near the pulsation frequency around 0.23 Hz

Gene frequencies of BoLA-DRB3 alleles estimated through sequence-based typing (PCR-SBT) in a Holstein population of La Pampa province

El objetivo del presente estudio consistió en estimar las frecuencias alélicas del exón 2 del gen de Clase II del Sistema Principal de Histocompatibilidad BoLA-DRB3 en una población de ganado Holstein de la provincia de La Pampa. Los polimorfismos presentes en el exón 2 del gen BoLA-DRB3 se identificaron mediante la técnica de secuenciación directa (PCR-SBT). Los resultados obtenidos permitieron detectar un total de 21 alelos con un rango de frecuencia de 0,014 a 0,222. Esto resultó en una heterocigosidad esperada de 0,91. Estos resultados se compararon con los reportados para ganado Holstein de Japón, evidenciando que con la excepción del alelo BoLA-DRB3*1201, ambas poblaciones presentaron los mismo alelos mayoritarios (BoLA-DRB3*1101, *1501 y *0101). Este resultado sería consecuencia del alto nivel de homogeneidad exhibido por esta raza, debido al uso de la misma genética a nivel global.The objective of this study was to estimate allele frequencies of the BoLA-DRB3 exon 2 in a Holstein population from La Pampa province. The exon 2 polymorphisms were genotyped by sequence-based typing method (PCR-SBT). In the studied herd, a total of 21 variants were detected, ranging from 0.014 to 0.222. This resulted in an expected heterozygocity of 0.91. Obtained data were compared with those reported for Japanese Holstein population, showing that with the exception of BoLA-DRB3*1201 allele, both populations shared the same major variants (BoLA-DRB3*1101, *1501 and *0101). This result could be consequence of the high level of homogeneity present in Holstein breed, due to the use of same genetic on the whole world.Fil: Baltian, Laura Rosana. Universidad Nacional de La Pampa. Facultad de Ciencias Veterinarias; ArgentinaFil: Ripoli, María Verónica. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico CONICET- La Plata. Instituto de Genética Veterinaria "Ing. Fernando Noel Dulout". Universidad Nacional de La Plata. Facultad de Ciencias Veterinarias. Instituto de Genética Veterinaria; ArgentinaFil: Takeshima, S. N.. Riken. Viral Infectious Diseases Unit; JapónFil: Aida, Y.. Riken. Viral Infectious Diseases Unit; JapónFil: Giovambattista, Guillermo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico CONICET- La Plata. Instituto de Genética Veterinaria "Ing. Fernando Noel Dulout". Universidad Nacional de La Plata. Facultad de Ciencias Veterinarias. Instituto de Genética Veterinaria; Argentin

ASCA Observations of the Jet Source XTE J1748-288

XTE J1748-288 is a new X-ray transient with a one-sided radio jet. It was observed with ASCA on 1998/09/06 and 1998/09/26, 100 days after the onset of the radio-X-ray outburst. The spectra were fitted with an attenuated power-law model, and the 2-6-keV flux was 4.6 * 10^{-11} erg s^{-1} cm^{-2} and 2.2 * 10^{-12} on 09/06 and 09/26, respectively. The light curve showed that the steady exponential decay with an e-folding time of 14 days lasted over 100 days and 4 orders of magnitude from the peak of the outburst. The celestial region including the source had been observed with ASCA on 1993/10/01 and 1994/09/22, years before the discovery. In those period, the flux was < 10^{-13} erg s^{-1} cm^{-2}, below ASCA's detection limit. The jet blob colliding to the environmental matter was supposedly not the X-ray source, although the emission mechanism has not been determined. A possible detection of a K line from highly ionized iron is discussed.Comment: 11 pages, 4 figures, submitted to ApJL. Fig2 is replaced with correct on

Estimation of bovine leukemia virus (BLV) proviral load harbored by lymphocyte subpopulations in BLV-infected cattle at the subclinical stage of enzootic bovine leucosis using BLV-CoCoMo-qPCR

Background: Bovine leukemia virus (BLV) is associated with enzootic bovine leukosis (EBL), which is the most common neoplastic disease of cattle. BLV infection may remain clinically silent at the aleukemic (AL) stage, cause persistent lymphocytosis (PL), or, more rarely, B cell lymphoma. BLV has been identified in B cells, CD2+ T cells, CD3+ T cells, CD4+ T cells, CD8+ T cells, γ/δ T cells, monocytes, and granulocytes in infected cattle that do not have tumors, although the most consistently infected cell is the CD5+ B cell. The mechanism by which BLV causes uncontrolled CD5+ B cell proliferation is unknown. Recently, we developed a new quantitative real-time polymerase chain reaction (PCR) method, BLV-CoCoMo-qPCR, which enabled us to demonstrate that the proviral load correlates not only with BLV infection, as assessed by syncytium formation, but also with BLV disease progression. The present study reports the distribution of BLV provirus in peripheral blood mononuclear cell subpopulations isolated from BLV-infected cows at the subclinical stage of EBL as examined by cell sorting and BLV-CoCoMo-qPCR.Results: Phenotypic characterization of five BLV-infected but clinically normal cattle with a proviral load of > 100 copies per 1 × 105 cells identified a high percentage of CD5+ IgM+ cells (but not CD5- IgM+ B cells, CD4+ T cells, or CD8+T cells). These lymphocyte subpopulations were purified from three out of five cattle by cell sorting or using magnetic beads, and the BLV proviral load was estimated using BLV-CoCoMo-qPCR. The CD5+ IgM+ B cell population in all animals harbored a higher BLV proviral load than the other cell populations. The copy number of proviruses infecting CD5- IgM+ B cells, CD4+ cells, and CD8+ T cells (per 1 ml of blood) was 1/34 to 1/4, 1/22 to 1/3, and 1/31 to 1/3, respectively, compared with that in CD5+ IgM+ B cells. Moreover, the BLV provirus remained integrated into the genomic DNA of CD5+ IgM+ B cells, CD5- IgM+ B cells, CD4+ T cells, and CD8+ T cells, even in BLV-infected cattle with a proviral load of <100 copies per 105 cells.Conclusions: The results of the recent study showed that, although CD5+ IgM+ B cells were the main cell type targeted in BLV-infected but clinically normal cattle, CD5- IgM+ B cells, CD4+ cells, and CD8+ T cells were infected to a greater extent than previously thought.Facultad de Ciencias Veterinaria

Auger Recombination in Semiconductor Quantum Wells

The principal mechanisms of Auger recombination of nonequilibrium carriers in semiconductor heterostructures with quantum wells are investigated. It is shown for the first time that there exist three fundamentally different Auger recombination mechanisms of (i) thresholdless, (ii) quasi-threshold, and (iii) threshold types. The rate of the thresholdless Auger process depends on temperature only slightly. The rate of the quasi-threshold Auger process depends on temperature exponentially. However, its threshold energy essentially varies with quantum well width and is close to zero for narrow quantum wells. It is shown that the thresholdless and the quasi-threshold Auger processes dominate in narrow quantum wells, while the threshold and the quasi-threshold processes prevail in wide quantum wells. The limiting case of a three-dimensional (3D)Auger process is reached for infinitely wide quantum wells. The critical quantum well width is found at which the quasi-threshold and threshold Auger processes merge into a single 3D Auger process. Also studied is phonon-assisted Auger recombination in quantum wells. It is shown that for narrow quantum wells the act of phonon emission becomes resonant, which in turn increases substantially the coefficient of phonon-assisted Auger recombination. Conditions are found under which the direct Auger process dominates over the phonon-assisted Auger recombination at various temperatures and quantum well widths.Comment: 38 pages, 7 figure

Magnetic Fields of Accreting X-Ray Pulsars with the Rossi X-Ray Timing Explorer

Using a consistent set of models, we parameterized the X-ray spectra of all accreting pulsars in the Rossi X-ray Timing Explorer database which exhibit Cyclotron Resonance Scattering Features (CRSFs, or cyclotron lines). These sources in our sample are Her X-1, 4U 0115+63, Cen X-3, 4U 1626-67, XTE J1946-274, Vela X-1, 4U 1907+09, 4U 1538-52, GX 301-2, and 4U 0352+309 (X Per). We searched for correlations among the spectral parameters, concentrating on how the cyclotron line energy relates to the continuum and therefore how the neutron star B-field influences the X-Ray emission. As expected, we found a correlation between the CRSF energy and the spectral cutoff energy. However, with our consistent set of fits we found that the relationship is more complex than what has been reported previously. Also, we found that not only does the width of the cyclotron line correlate with the energy (as suggested by theory), but that the width scaled by the energy correlates with the depth of the feature. We discuss the implications of these results, including the possibility that accretion directly affects the relative alignment of the neutron star spin and dipole axes. Lastly, we comment on the current state of fitting phenomenological models to spectra in the RXTE/BeppoSAX era and the need for better theoretical models of the X-Ray continua of accreting pulsars.Comment: 36 Pages, 9 Figures, 9 Tables, ApJ in pres

Estimation of bovine leukemia virus (BLV) proviral load harbored by lymphocyte subpopulations in BLV-infected cattle at the subclinical stage of enzootic bovine leucosis using BLV-CoCoMo-qPCR

Background: Bovine leukemia virus (BLV) is associated with enzootic bovine leukosis (EBL), which is the most common neoplastic disease of cattle. BLV infection may remain clinically silent at the aleukemic (AL) stage, cause persistent lymphocytosis (PL), or, more rarely, B cell lymphoma. BLV has been identified in B cells, CD2+ T cells, CD3+ T cells, CD4+ T cells, CD8+ T cells, γ/δ T cells, monocytes, and granulocytes in infected cattle that do not have tumors, although the most consistently infected cell is the CD5+ B cell. The mechanism by which BLV causes uncontrolled CD5+ B cell proliferation is unknown. Recently, we developed a new quantitative real-time polymerase chain reaction (PCR) method, BLV-CoCoMo-qPCR, which enabled us to demonstrate that the proviral load correlates not only with BLV infection, as assessed by syncytium formation, but also with BLV disease progression. The present study reports the distribution of BLV provirus in peripheral blood mononuclear cell subpopulations isolated from BLV-infected cows at the subclinical stage of EBL as examined by cell sorting and BLV-CoCoMo-qPCR.Results: Phenotypic characterization of five BLV-infected but clinically normal cattle with a proviral load of > 100 copies per 1 × 105 cells identified a high percentage of CD5+ IgM+ cells (but not CD5- IgM+ B cells, CD4+ T cells, or CD8+T cells). These lymphocyte subpopulations were purified from three out of five cattle by cell sorting or using magnetic beads, and the BLV proviral load was estimated using BLV-CoCoMo-qPCR. The CD5+ IgM+ B cell population in all animals harbored a higher BLV proviral load than the other cell populations. The copy number of proviruses infecting CD5- IgM+ B cells, CD4+ cells, and CD8+ T cells (per 1 ml of blood) was 1/34 to 1/4, 1/22 to 1/3, and 1/31 to 1/3, respectively, compared with that in CD5+ IgM+ B cells. Moreover, the BLV provirus remained integrated into the genomic DNA of CD5+ IgM+ B cells, CD5- IgM+ B cells, CD4+ T cells, and CD8+ T cells, even in BLV-infected cattle with a proviral load of <100 copies per 105 cells.Conclusions: The results of the recent study showed that, although CD5+ IgM+ B cells were the main cell type targeted in BLV-infected but clinically normal cattle, CD5- IgM+ B cells, CD4+ cells, and CD8+ T cells were infected to a greater extent than previously thought.Facultad de Ciencias Veterinaria

Chemical treatment enhances skipping of a mutated exon in the dystrophin gene

Duchenne muscular dystrophy (DMD) is a fatal muscle wasting disease caused by a loss of the dystrophin protein. Control of dystrophin mRNA splicing to convert severe DMD to a milder phenotype is attracting much attention. Here we report a dystrophinopathy patient who has a point mutation in exon 31 of the dystrophin gene. Although the mutation generates a stop codon, a small amount of internally deleted, but functional, dystrophin protein is produced in the patient cells. An analysis of the mRNA reveals that the mutation promotes exon skipping and restores the open reading frame of dystrophin. Presumably, the mutation disrupts an exonic splicing enhancer and creates an exonic splicing silencer. Therefore, we searched for small chemicals that enhance exon skipping, and found that TG003 promotes the skipping of exon 31 in the endogenous dystrophin gene in a dose-dependent manner and increases the production of the dystrophin protein in the patient's cells

Simulation of developmental changes in action potentials with ventricular cell models

During cardiomyocyte development, early embryonic ventricular cells show spontaneous activity that disappears at a later stage. Dramatic changes in action potential are mediated by developmental changes in individual ionic currents. Hence, reconstruction of the individual ionic currents into an integrated mathematical model would lead to a better understanding of cardiomyocyte development. To simulate the action potential of the rodent ventricular cell at three representative developmental stages, quantitative changes in the ionic currents, pumps, exchangers, and sarcoplasmic reticulum (SR) Ca2+ kinetics were represented as relative activities, which were multiplied by conductance or conversion factors for individual ionic systems. The simulated action potential of the early embryonic ventricular cell model exhibited spontaneous activity, which ceased in the simulated action potential of the late embryonic and neonatal ventricular cell models. The simulations with our models were able to reproduce action potentials that were consistent with the reported characteristics of the cells in vitro. The action potential of rodent ventricular cells at different developmental stages can be reproduced with common sets of mathematical equations by multiplying conductance or conversion factors for ionic currents, pumps, exchangers, and SR Ca2+ kinetics by relative activities