Histological and ultrastructural feature and nitrite production of caprine preantral follicles in vitro cultured in the presence or absence of serum

Avaliou-se o efeito da adição de diferentes tipos e concentrações de soro sobre o desenvolvimento e a sobrevivência de folículos ovarianos pré-antrais (FOPA) caprinos in vitro. Além disso, verificou-se a relação entre as concentrações de nitrito presentes no meio de cultivo e a viabilidade folicular. Cada par ovariano foi dividido em 29 fragmentos, sendo um destinado ao controle. Os fragmentos foram cultivados por um ou sete dias em meio essencial mínimo suplementado (MEM+) ou MEM+ com diferentes concentrações (10 ou 20%) de soro fetal bovino (SFB), soro de cabra em estro (SCE) ou soro de cabra em diestro (SCD). Na análise morfológica após sete dias, apenas o tratamento com 10% de SFB apresentou percentual de FOPA normais similar ao MEM+ (P>0,05). A análise ultra-estrutural dos folículos cultivados por sete dias com MEM+ ou MEM+ com 10% de SFB mostrou danos oocitários, porém células da granulosa normais. A análise do meio de cultivo revelou correlação positiva entre a viabilidade folicular e a produção de nitrito. A suplementação com soro não melhorou a viabilidade de FOPA e a concentração de nitrito no meio de cultivo funcionou como um indicador da viabilidade das células da granulosa de FOPA caprinos cultivados in vitro. ______________________________________________________________________________________________________________ ABSTRACTThe effect of the addition of different types and concentrations of sera on the viability and development of caprine preantal follicles (PAF) in vitro cultured was analyzed. In addition, it was evaluated the correlation between nitrite concentrations in culture medium and folicular viability. Each ovarian pair was divided in 29 fragments and one was used as control. The fragments were cultured for one or seven days in minimal essential medium (MEM+) or MEM+ with different concentrations of (10 or 20%) bovine fetal serum (BFS), estrous goat serum (EGS), or diestrous goat serum (DGS). After seven days, the morphological analysis showed that only the treatment with 10% BFS maintained the percentage of normal PAF similar to MEM+ (P>0.05). The ultrastructural analysis of follicles cultured for seven days in MEM+ or MEM+ with 10% BFS showed some oocyte damage, although the granulosa cells were normal. Analysis of culture medium revealed a positive correlation between follicular viability and nitrite production. Supplementation with serum did not improve the viability of PAF and nitrite levels in culture medium served as an indicator of viability of granulose cells from caprine PAF in vitro cultured

Asymptotics of orthogonal polynomials for a weight with a jump on [−1,1]

We consider the orthogonal polynomials on [-1, 1] with respect to the weight w(c)(x) = h(x)(1 - x)(alpha) (1+ x)beta Xi(c)(x), alpha, beta > -1, where h is real analytic and strictly positive on [-1, 1] and Xi(c) is a step-like function: Xi(c)(x) = 1 for x is an element of [-1, 0) and Xi(c) (x) = c(2), c > 0, for x is an element of [0, 1]. We obtain strong uniform asymptotics of the monic orthogonal polynomials in C, as well as first terms of the asymptotic expansion of the main parameters (leading coefficients of the orthonormal polynomials and the recurrence coefficients) as n -> infinity. In particular, we prove for w(c) a conjecture of A. Magnus regarding the asymptotics of the recurrence coefficients. The main focus is on the local analysis at the origin. We study the asymptotics of the Christoffel-Darboux kernel in a neighborhood of the jump and show that the zeros of the orthogonal polynomials no longer exhibit clock behavior. For the asymptotic analysis we use the steepest descent method of Deift and Zhou applied to the noncommutative Riemann-Hilbert problems characterizing the orthogonal polynomials. The local analysis at x = 0 is carried out in terms of confluent hypergeometric functions. Incidentally, we establish some properties of these functions that may have an independent interest.Junta de Andalucía-Spain- FQM-229 and P06- FQM-01735.Ministry of Science and Innovation of Spain - MTM2008-06689-C02-01FCT -SFRH/BD/29731/200

Shedding light on zooplankton diversity from the Congo River Basin

peer reviewedThe Congo River Basin is the second largest in the world, and its plankton biota remains completely unknown. We studied the zooplankton diversity across 1700 km of the main channel (from the cities of Kisangani to Kinshasa) and subsequently in the mouths of the 25 largest tributaries during 2013 (N=39), and across 500 km of Kasai-Kwa River and tributaries in 2015 (N=25). We recorded 135 zooplankton species (26 for Testate Amoebae, 56 for Rotifera, 27 for Cladocera and 26 for Copepoda). At least five cladoceran and four copepod species are new. A non-metric multidimensional statistical analysis with Bray Curtis dissimilarity revealed that the zooplankton composition within Congo main channel was more similar than within the mouths of several tributaries and the Kasai-Kwa River basin. In the later, the tributaries were distinct from each other and from the main channel of Kasai River. A distance-based redundancy analysis using Bray-Curtis dissimilarity on abundance data revealed two main groups of species and limnological variables, one comprising sites with high total suspended matter, conductivity, chlorophyll, phytoplanktonabundance (white water rivers), and other with sites with high transparency and dissolved organic carbon concentration (black water rivers). Zooplankton diversity was uniform in the Congo main channel and in the Kasai-Kwa River, with low difference among sites. There was also a distinct third group, unrelated to variables. This study reveals a high diverse zooplankton community in the Congo basin, with new species and distinct community between the studied rivers, but homogeneous along each one

GWAS for Systemic Sclerosis Identifies Multiple Risk Loci and Highlights Fibrotic and Vasculopathy Pathways

Systemic sclerosis (SSc) is an autoimmune disease that shows one of the highest mortality rates among rheumatic diseases. We perform a large genome-wide association study (GWAS), and meta-analysis with previous GWASs, in 26,679 individuals and identify 27 independent genome-wide associated signals, including 13 new risk loci. The novel associations nearly double the number of genome-wide hits reported for SSc thus far. We define 95% credible sets of less than 5 likely causal variants in 12 loci. Additionally, we identify specific SSc subtype-associated signals. Functional analysis of high-priority variants shows the potential function of SSc signals, with the identification of 43 robust target genes through HiChIP. Our results point towards molecular pathways potentially involved in vasculopathy and fibrosis, two main hallmarks in SSc, and highlight the spectrum of critical cell types for the disease. This work supports a better understanding of the genetic basis of SSc and provides directions for future functional experiments.Funding: This work was supported by Spanish Ministry of Economy and Competitiveness (grant ref. SAF2015-66761-P), Consejeria de Innovacion, Ciencia y Tecnologia, Junta de Andalucía (P12-BIO-1395), Ministerio de Educación, Cultura y Deporte through the program FPU, Juan de la Cierva fellowship (FJCI-2015-24028), Red de Investigación en Inflamación y Enfermadades Reumaticas (RIER) from Instituto de Salud Carlos III (RD16/0012/0013), and Scleroderma Research Foundation and NIH P50-HG007735 (to H.Y.C.). H.Y.C. is an Investigator of the Howard Hughes Medical Institute. PopGen 2.0 is supported by a grant from the German Ministry for Education and Research (01EY1103). M.D.M and S.A. are supported by grant DoD W81XWH-18-1-0423 and DoD W81XWH-16-1-0296, respectively

7th Drug hypersensitivity meeting: part two

No abstract availabl

Velocity-space sensitivity of the time-of-flight neutron spectrometer at JET

The velocity-space sensitivities of fast-ion diagnostics are often described by so-called weight functions. Recently, we formulated weight functions showing the velocity-space sensitivity of the often dominant beam-target part of neutron energy spectra. These weight functions for neutron emission spectrometry (NES) are independent of the particular NES diagnostic. Here we apply these NES weight functions to the time-of-flight spectrometer TOFOR at JET. By taking the instrumental response function of TOFOR into account, we calculate time-of-flight NES weight functions that enable us to directly determine the velocity-space sensitivity of a given part of a measured time-of-flight spectrum from TOFOR

Relationship of edge localized mode burst times with divertor flux loop signal phase in JET

A phase relationship is identified between sequential edge localized modes (ELMs) occurrence times in a set of H-mode tokamak plasmas to the voltage measured in full flux azimuthal loops in the divertor region. We focus on plasmas in the Joint European Torus where a steady H-mode is sustained over several seconds, during which ELMs are observed in the Be II emission at the divertor. The ELMs analysed arise from intrinsic ELMing, in that there is no deliberate intent to control the ELMing process by external means. We use ELM timings derived from the Be II signal to perform direct time domain analysis of the full flux loop VLD2 and VLD3 signals, which provide a high cadence global measurement proportional to the voltage induced by changes in poloidal magnetic flux. Specifically, we examine how the time interval between pairs of successive ELMs is linked to the time-evolving phase of the full flux loop signals. Each ELM produces a clear early pulse in the full flux loop signals, whose peak time is used to condition our analysis. The arrival time of the following ELM, relative to this pulse, is found to fall into one of two categories: (i) prompt ELMs, which are directly paced by the initial response seen in the flux loop signals; and (ii) all other ELMs, which occur after the initial response of the full flux loop signals has decayed in amplitude. The times at which ELMs in category (ii) occur, relative to the first ELM of the pair, are clustered at times when the instantaneous phase of the full flux loop signal is close to its value at the time of the first ELM