Dual encoding of muscle tension and eye position by abducens motoneurons

Extraocular muscle tension associated with spontaneous eye movements has a pulse-slide-step profile similar to that of motoneuron firing rate. Existing models only relate motoneuron firing to eye position, velocity and acceleration. We measured and quantitatively compared lateral rectus muscle force and eye position with the firing of abducens motoneurons in the cat to determine fundamental encoding correlations. During fixations (step), muscle force increased exponentially with eccentric eye position, consistent with a model of estimate ensemble motor innervation based on neuronal sensitivities and recruitment order. Moreover, firing rate in all motoneurons tested was better related to eye position than to muscle tension during fixations. In contrast, during the postsaccadic slide phase, the time constant of firing rate decay was closely related to that of muscle force decay, suggesting that all motoneurons encode muscle tension as well. Discharge characteristics of abducens motoneurons formed overlapping clusters of phasic and tonic motoneurons, thus, tonic units recruited earlier and had a larger slide signal. We conclude that the slide signal is a discharge characteristic of the motoneuron that controls muscle tension during the postsaccadic phase and that motoneurons are specialized for both tension and position-related properties. The organization of signal content in the pool of abducens motoneurons from the very phasic to the very tonic units is possibly a result of the differential trophic background received from distinct types of muscle fibers

Emission Minimization of a Two-Stage Sour Water Stripping Unit Using Surrogate Models for Improving Heat Duty Control

Sour water are aqueous waste streams from oil refining operations, heavily contaminated with hydrogen sulfide and ammonia, which need to be stripped before reuse or disposal, avoiding damages to process and environment. Two-stage sour water stripper units are the most common technology to treat sour water for hydrogen sulfide and ammonia separation to produce reusable water and send these species respectively to Claus and ammonia plants. The first stage of a two-stage sour water unit is responsible for properly splitting hydrogen sulfide and ammonia. This work uses surrogate models to predict the limiting point of hydrogen sulfide separation in the first stage of a sour water unit, allowing more efficient heat duty control strategies to achieve the difficult split of hydrogen sulfide and ammonia and simultaneously lowering heat consumption. Failure of compliance to this limit results in unspecified stripped gas from the first stage, impeding it to directed to Claus plant, entailing loss of sulfur production and higher load of pollutant emissions from flared gases. Therefore, a precise surrogate predictor was developed to dynamically define a quasi-optimum set-point to the controller of the first stage reboiler duty based on dynamic disturbances – the first stage input factors to the surrogate model, such as hydrogen sulfide and ammonia contents of the sour water. The new control policy outperformed the traditional first stage ratio control in terms of stripped gas composition and plant stability

Coral Disease and Health Workshop: Coral Histopathology II

The health and continued existence of coral reef ecosystems are threatened by an increasing array of environmental and anthropogenic impacts. Coral disease is one of the prominent causes of increased mortality among reefs globally, particularly in the Caribbean. Although over 40 different coral diseases and syndromes have been reported worldwide, only a few etiological agents have been confirmed; most pathogens remain unknown and the dynamics of disease transmission, pathogenicity and mortality are not understood. Causal relationships have been documented for only a few of the coral diseases, while new syndromes continue to emerge. Extensive field observations by coral biologists have provided substantial documentation of a plethora of new pathologies, but our understanding, however, has been limited to descriptions of gross lesions with names reflecting these observations (e.g., black band, white band, dark spot). To determine etiology, we must equip coral diseases scientists with basic biomedical knowledge and specialized training in areas such as histology, cell biology and pathology. Only through combining descriptive science with mechanistic science and employing the synthesis epizootiology provides will we be able to gain insight into causation and become equipped to handle the pending crisis. One of the critical challenges faced by coral disease researchers is to establish a framework to systematically study coral pathologies drawing from the field of diagnostic medicine and pathology and using generally accepted nomenclature. This process began in April 2004, with a workshop titled Coral Disease and Health Workshop: Developing Diagnostic Criteria co-convened by the Coral Disease and Health Consortium (CDHC), a working group organized under the auspices of the U.S. Coral Reef Task Force, and the International Registry for Coral Pathology (IRCP). The workshop was hosted by the U.S. Geological Survey, National Wildlife Health Center (NWHC) in Madison, Wisconsin and was focused on gross morphology and disease signs observed in the field. A resounding recommendation from the histopathologists participating in the workshop was the urgent need to develop diagnostic criteria that are suitable to move from gross observations to morphological diagnoses based on evaluation of microscopic anatomy. (PDF contains 92 pages

Lesão do esmalte após remoção de adesivo ortodontico por pedra de Arkansas e pontas laminadas de carbeto de tungsténio

Objectives: The main aim of this study was to compare the effectiveness of two different methods to remove orthodontic composite adhesives from enamel concerning the surface damage and remnant composite adhesive on the surfaces. Methods: Human molars were stored in buffer solution at room temperature before bonding the brackets. Teeth were ultrasonically cleaned in distilled water before bonding procedure. Ninety two brackets were randomly bonded to the buccal surface of twenty three molars using a composite-based adhesive system. After 15 days, the orthodontic composite adhesives were removed by using Arkansas' stone or multi-blade tungsten burs. After debonding process, the remnant composite adhered to the tooth as well as the teeth surfaces were analyzed by photographic images at x40 magnification concerning the (ARI) adhesive remnant or (SRI) surface roughness index. Also, enamel surfaces were inspected by field emission guns scanning electron microscopy (FEGSEM) before bonding and after bracket detachment. The statistical analysis was performed using SPSS® Statistics vs.18.0, considering a significance level of 0.05 to one-way ANOVA. Tukey's test was used for multiple comparisons and Chi-square tests were used to analyze the association between categorical variables. Results: ARI results revealed no statistically significant differences between the two methods of bracket removal (p=0.283). Considering SRI, statistically significant differences were detected between the two procedures (p<0.001) considering all worn surfaces revealed lower surface roughness after removal of adhesive by Arkansas stone than that recorded on worn surfaces after removal using tungsten carbide burs. Conclusion: The removal of orthodontic adhesive promoted less damage on enamel surfaces by using Arkansas stone at low rotation. Nevertheless, finishing procedures can decrease the roughness on enamel without additional damage.Objetivos: O objetivo deste estudo foi comparar a eficácia de dois métodos diferentes de remocâo do compósito utilizado na adesão de brackets, após a realizacão do tratamento ortodôntico. Métodos: Foram utilizados 92 brackets colados em 23 molares previamente selecionados de acordo com os critérios de inclusão/exclusão. Uma vez removidos os brackets, foram então utilizados os dois métodos de remocão de compósito: a) pedras de Arkansas; b) brocas multilaminadas de tungsténio, ambas utilizadas em contra-ângulo (baixa rotacão). Uma vez removido o compósito, foram analisadas e quantificadas as possíveis lesões advindas do procedimento. A área de compósito remanescente foi calculada em todos os dentes. A aná- lise estatística foi realizada utilizando o SPSS® Statistics vs.18.0, considerando um nível de significância de 0,05 para teste ANOVA. O teste de Tukey foi utilizado para comparações múltiplas e Qui-quadrado para análise entre variáveis categóricas. Resultados: Após a remocão do compósito com cada um dos métodos verificou-se que, relativamente ao índice adesivo remanescente (IAR), não existiam diferença estatisticamente significativa (p=0,283) entre métodos de remoção. Entretanto, diferenças em relação ao índice de rugosidade de superfície (IRS) foram estatisticamente significativas (p<0,001) com resultados a favor do método utilizando pedras de Arkansas. Conclusão: Menor dano ao esmalte foi promovido pela remocão de adesivo ortodóntico com uso da pedra de Arkansas. Entretanto, polimento adicional diminui a rugosidade da superfície sem danos adicionais ao esmalte.This work has been supported by FCT (Fundação para a Ciência e Tecnologia – Portugal) in the scope of the project UID/ EEA/04436/ 2013 NORTE-01-0145- FEDER-000018 - HAMaBIC

A Bayesian approach to single-particle electron cryo-tomography in RELION-4.0

We present a new approach for macromolecular structure determination from multiple particles in electron cryo-tomography (cryo-ET) data sets. Whereas existing subtomogram averaging approaches are based on 3D data models, we propose to optimise a regularised likelihood target that approximates a function of the 2D experimental images. In addition, analogous to Bayesian polishing and contrast transfer function (CTF) refinement in single-particle analysis, we describe the approaches that exploit the increased signal-to-noise ratio in the averaged structure to optimise tilt-series alignments, beam-induced motions of the particles throughout the tilt-series acquisition, defoci of the individual particles, as well as higher-order optical aberrations of the microscope. Implementation of our approaches in the open-source software package RELION aims to facilitate their general use, particularly for those researchers who are already familiar with its single-particle analysis tools. We illustrate for three applications that our approaches allow structure determination from cryo-ET data to resolutions sufficient for de novo atomic modelling.This work was funded by the UK Research and Innovation (UKRI) Medical Research Council (MC_UP_A025_1013 to SHWS; and MC_UP_1201/16 to JAGB), the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation program (ERC-CoG-2014, grant 648432, MEMBRANEFUSION to JAGB and ERC StG-2019, grant 852915 CRYTOCOP to GZ); the Swiss National Science Foundation (grant 205321_179041/1 to DC-D), the Max Planck Society (to JAGB) and the UKRI Biotechnology and Biological Sciences Research Council (grant BB/T002670/1 to GZ). TAMB is a recipient of a Sir Henry Dale Fellowship, jointly funded by the Wellcome Trust and the Royal Society (202231/Z/16/Z). JZ was partially funded by the European Union’s Horizon 2020 research and innovation program (ERC-ADG-2015, grant 692726, GlobalBioIm to Michael Unser)

Reactive oxygen species production and redox state in parthenogenetic and sperm-mediated bovine oocyte activation

The knowledge concerning redox and reactive oxygen species (ROS)-mediated regulation of early embryo development is scarce and remains controversial. The aim of this work was to determine ROS production and redox state during early in vitro embryo development in sperm-mediated and parthenogenetic activation of bovine oocytes. Sperm-mediated oocyte activation was carried out in IVF-modified synthetic oviductal fluid (mSOF) with frozen-thawed semen. Parthenogenetic activation was performed in TALP plus ionomycin and then in IVF-mSOF with 6-dimethylaminopurine plus cytochalasin B. Embryos were cultured in IVF-mSOF. ROS and redox state were determined at each 2-h interval (7-24 h from activation) by 2',7'-dichlorodihydrofluorescein diacetate and RedoxSensor Red CC-1 fluorochromes respectively. ROS levels and redox state differed between activated and non-activated oocytes (P<0.05 by ANOVA). In sperm-activated oocytes, an increase was observed between 15 and 19 h (P<0.05). Conversely, in parthenogenetically activated oocytes, we observed a decrease at 9 h (P<0.05). In sperm-activated oocytes, ROS fluctuated throughout the 24 h, presenting peaks around 7, 19, and 24 h (P<0.05), while in parthenogenetic activation, peaks were detected at 7, 11, and 17 h (P<0.05). In the present work, we found clear distinctive metabolic patterns between normal and parthenogenetic zygotes. Oxidative activity and ROS production are an integral part of bovine zygote behavior, and defining a temporal pattern of change may be linked with developmental competence.S Morado, P Cetica, M Beconi, J G Thompson and G Dalvi

Evidence of association of the NLRP1 gene with giant cell arteritis

Recent studies have focused attention on the involvement of NLRP1 to confer susceptibility for extended autoimmune/inflammatory disorders, being considered a common risk factor in autoimmunity. NLRP1 provides a scaffold for the assembly of the inflammasome that activates caspases 1 and 5, required for processing and activation of the proinflammatory cytokines interleukin 1β (IL-1β), IL-18 and IL-33 and promoting inflammation

Influence of the IL17A locus in giant cell arteritis susceptibility

Objective: Different lines of evidence have highlighted the role of IL-17A in the inflammatory process occurring in giant cell arteritis (GCA). The aim of the present study was to assess whether the IL17A locus influences GCA susceptibility and its clinical subphenotypes. Methods: We carried out a large meta-analysis including a total of 1266 biopsy-proven GCA patients and 3779 healthy controls from four European populations (Spain, Italy, Germany and Norway). Five IL17A polymorphisms (rs4711998, rs8193036, rs3819024, rs2275913 and rs7747909) were selected by tagging and genotyped using TaqMan assays. Allelic combination and dependency tests were also performed. Results: In the pooled analysis, two of the five analysed polymorphisms showed evidence of association with GCA (rs2275913: PMH=1.85E−03, OR=1.17 (1.06-1.29); rs7747909: PMH=8.49E-03, OR=1.15 (1.04-1.27)). A clear trend of association was also found for the rs4711998 variant (PMH=0.059, OR=1.11 (1.00-1.23)). An independent effect of rs2275913 and rs4711998 was evident by conditional regression analysis. In addition, the haplotype harbouring the risk alleles better explained the observed association than the polymorphisms independently (likelihood p value <10−05). Conclusions: Polymorphisms within the IL17A locus show a novel association with GCA. This finding supports the relevant role of the Th17 cells in this vasculitis pathophysiology

Identification of the PTPN22 functional variant R620W as susceptibility genetic factor for giant cell arteritis

Objective: To analyse the role of the PTPN22 and CSK genes, previously associated with autoimmunity, in the predisposition and clinical phenotypes of giant cell arteritis (GCA). Methods: Our study population was composed of 911 patients diagnosed with biopsy-proven GCA and 8136 unaffected controls from a Spanish discovery cohort and three additional independent replication cohorts from Germany, Norway and the UK. Two functional PTPN22 polymorphisms (rs2476601/R620W and rs33996649/R263Q) and two variants of the CSK gene (rs1378942 and rs34933034) were genotyped using predesigned TaqMan assays. Results: The analysis of the discovery cohort provided evidence of association of PTPN22 rs2476601/R620W with GCA (PFDR=1.06E-04, OR=1.62, CI 95% 1.29 to 2.04). The association did not appear to follow a specific GCA subphenotype. No statistically significant differences between allele frequencies for the other PTPN22 and CSK genetic variants were evident either in the case/control or in stratified case analysis. To confirm the detected PTPN22 association, three replication cohorts were genotyped, and a consistent association between the PTPN22 rs2476601/R620W variant and GCA was evident in the overall meta-analysis (PMH=2.00E-06, OR=1.51, CI 95% 1.28 to 1.79). Conclusions: Our results suggest that the PTPN22 polymorphism rs2476601/R620W plays an important role in the genetic risk to GCA