424 research outputs found
Elevated immune gene expression is associated with poor reproductive success of urban blue tits
Urban and forest habitats differ in many aspects that can lead to modifications of the immune system of wild animals. Altered parasite communities, pollution, and artificial light at night in cities have been associated with exacerbated inflammatory responses, with possibly negative fitness consequences, but few data are available from free-living animals. Here, we investigate how urbanization affects major immune pathways and experimentally test potentially contributing factors in blue tits (Cyanistes caeruleus) from an urban and forest site. We first compared breeding adults by quantifying the mRNA transcript levels of proteins associated with anti-bacterial, anti-malarial (TLR4, LY86) and anti-helminthic (Type 2 transcription factor GATA3) immune responses. Adult urban and forest blue tits differed in gene expression, with significantly increased TLR4 and GATA3, but not LY86, in the city. We then experimentally tested whether these differences were environmentally induced by cross-fostering eggs between the sites and measuring mRNA transcripts in nestlings. The populations differed in reduced reproductive success, with a lower fledging success and lower fledgling weight recorded at the urban site. This mirrors the findings of our twin study reporting that the urban site was severely resource limited when compared to the forest. Because of low urban survival, robust gene expression data were only obtained from nestlings reared in the forest. Transcript levels in these nestlings showed no (TLR4, LY86), or weak (GATA3), differences according to their origin from forest or city nests, suggesting little genetic or maternal contribution to nestling immune transcript levels. Lastly, to investigate differences in parasite pressure between urban and forest sites, we measured the prevalence of malaria in adult and nestling blood. Prevalence was invariably high across environments and not associated with the transcript levels of the studied immune genes. Our results support the hypothesis that inflammatory pathways are activated in an urban environment and suggest that these differences are most likely induced by environmental factors
Análisis de las diferencias de género en la elección de estudios universitarios
Esta investigación analiza el interés del
alumnado de Bachillerato por realizar una carrera universitaria
concreta y los motivos de dicha elección según
la variable sexo. Se utilizó un diseño de investigación
transversal con encuesta. Los resultados muestran
que las chicas eligen principalmente carreras de Humanidades,
Ciencias Experimentales, Ciencias Sociales,
Jurídicas y de la Salud y sus principales motivos de elección
son porque les gusta, por vocación y para ayudar a
otras personas, mientras que ellos se decantan por estudios
técnicos para ganar un buen sueldo. Se discute la
pertinencia de una orientación vocacional individualizada
que garantice la igualdad de oportunidades
In vivo sensitivity of the embryonic and adult neural stem cell compartments to low-dose radiation
The embryonic brain is radiation-sensitive, with cognitive deficits being observed after exposure to low radiation doses. Exposure of neonates to radiation can cause intracranial carcinogenesis. To gain insight into the basis underlying these outcomes, we examined the response of the embryonic, neonatal and adult brain to low-dose radiation, focusing on the neural stem cell compartments. This review summarizes our recent findings. At E13.5-14.5 the embryonic neocortex encompasses rapidly proliferating stem and progenitor cells. Exploiting mice with a hypomorphic mutation in DNA ligase IV (Lig4(Y288C) ), we found a high level of DNA double-strand breaks (DSBs) at E14.5, which we attribute to the rapid proliferation. We observed endogenous apoptosis in Lig4(Y288C) embryos and in WT embryos following exposure to low radiation doses. An examination of DSB levels and apoptosis in adult neural stem cell compartments, the subventricular zone (SVZ) and the subgranular zone (SGZ) revealed low DSB levels in Lig4(Y288C) mice, comparable with the levels in differentiated neuronal tissues. We conclude that the adult SVZ does not incur high levels of DNA breakage, but sensitively activates apoptosis; apoptosis was less sensitively activated in the SGZ, and differentiated neuronal tissues did not activate apoptosis. P5/P15 mice showed intermediate DSB levels, suggesting that DSBs generated in the embryo can be transmitted to neonates and undergo slow repair. Interestingly, this analysis revealed a stage of high endogenous apoptosis in the neonatal SVZ. Collectively, these studies reveal that the adult neural stem cell compartment, like the embryonic counterpart, can sensitively activate apoptosis
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Persistent recruitment of somatosensory cortex during active maintenance of hand images in working memory
Working memory (WM) supports temporary maintenance of task-relevant information. This process is associated with persistent activity in the sensory cortex processing the information (e.g., visual stimuli activate visual cortex). However, we argue here that more multifaceted stimuli moderate this sensory-locked activity and recruit distinctive cortices. Specifically, perception of bodies recruits somatosensory cortex (SCx) beyond early visual areas (suggesting embodiment processes). Here we explore persistent activation in processing areas beyond the sensory cortex initially relevant to the modality of the stimuli. Using visual and somatosensory evoked-potentials in a visual WM task, we isolated different levels of visual and somatosensory involvement during encoding of body and non-body-related images. Persistent activity increased in SCx only when maintaining body images in WM, whereas visual/posterior regions' activity increased significantly when maintaining non-body images. Our results bridge WM and embodiment frameworks, supporting a dynamic WM process where the nature of the information summons specific processing resources
Frame transformation and geoid undulation transfer to GNSS real time positions through the new RTCM 3.1 transformation messages
Radio Technical Commission for Marine Services (RTCM) standardised messages play an important
role in real time Global Navigation Satellite Systems (GNSS) applications such as navigation,
positioning, civil engineering, surveying, and cartographic or cadastral production. One of the latest
agreements on RTCM definitions contains the data fields for real time geodetic reference frame
transformation and orthometric heights computation by received geoid undulations via internet
protocol. These parameters can be generated dynamically by a GNSS data centre in a network of
reference stations, encapsulated in RTCM messages and broadcasted to the rover location so they
are centrally administered and the same frame transformations and geoid model are available to
every user in the field, obtaining results in a local reference frame in real time. This paper summarises
the functionality of the new RTCM 3?1 transformation messages, describes limitations and provides
ideas about the possible use for solving specific problems. Test field campaigns are used to
describe the real performance and usefulness of these new RTCM 3?1 messagesCapilla Roma, R.; Martín Furones, ÁE.; Anquela Julián, AB.; Berné Valero, JL. (2012). Frame transformation and geoid undulation transfer to GNSS real time positions through the new RTCM 3.1 transformation messages. Survey Review. 44(324):30-36. doi:10.1179/1752270611Y.0000000010S303644324Benciolini, B., Biagi, L., Crespi, M., Manzino, A. M., & Roggero, M. (2008). Reference frames for GNSS positioning services: Some problems and proposed solutions. Journal of Applied Geodesy, 2(1). doi:10.1515/jag.2008.006González-Matesanz, J., Dalda, A., & Malpica, J. A. (2006). A RANGE OF ED50-ETRS89 DATUM TRANSFORMATION MODELS TESTED ON THE SPANISH GEODETIC NETWORK. Survey Review, 38(302), 654-667. doi:10.1179/sre.2006.38.302.654Soler, T., & Marshall, J. (2003). A note on frame transformations with applications to geodetic datums. GPS Solutions, 7(2), 148-149. doi:10.1007/s10291-003-0063-
The neurobiological foundations of learning disabilities
Learning disabilities constitute a heterogeneous group of disorders that involve significant alterations in different cognitive domains (acquisition and use of language, reasoning, mathematical skills, visuospatial abilities, and so forth) that are not accounted for by a low level of intelligence, inadequate sociocultural development or lack of academic
opportunities. They result from an alteration in basic psychological processes, developmentally linked to an alteration in the central nervous system. Current functional neuroimaging techniques have made it possible to develop a new type of approach
to the neurofunctional foundations underlying these disorders, especially with regard to difficulties in the realm of reading/writing (developmental dyslexia) and attention deficit hyperactivity disorder (ADHD), which have their highest incidence among the infantile population of school-age children. Development. Neuroimaging studies have revealed a pattern of atypical activity in both kinds of disorders. In the case of dyslexia, alterations have been observed in the perisylvian circuits that underlie the mechanisms involved in reading skills. Studies into ADHD suggest a fronto-striatal dysfunction linked to the difficulties encountered to achieve inhibitory control, as well as alterations in the inferior parietal and posterior temporal cortex. Conclusions. Functional neuroimaging studies have shown that the clinical manifestations of these disorders are not only due to a dysfunction in specific areas of the brain, but also to alterations in the pattern of connectivityLas dificultades de aprendizaje comprenden un grupo heterogéneo de trastornos que implican alteraciones significativas en diferentes dominios cognitivos (adquisición y uso del lenguaje, razonamiento, habilidades matemáticas, visuoespaciales,
etc.) no justificadas por bajo nivel intelectual, desarrollo sociocultural inadecuado o falta de oportunidades académicas. Éstas son el resultado de una alteración en los procesos psicológicos básicos, evolutivamente ligados a una alteración del sistema nervioso central. Las actuales técnicas de neuroimagen funcional han permitido un nuevo tipo de acercamiento a las bases neurofuncionales de estos trastornos, particularmente de las dificultades en el ámbito de la lectoescritura (dislexia evolutiva) y del trastorno
por déficit de atención e hiperactividad (TDAH), los cuales tienen el mayor nivel de incidencia en la población escolar infantil. Desarrollo. Los estudios de neuroimagen han revelado un patrón de actividad atípico en ambos tipos de trastorno. En el caso de la dislexia, se han observado alteraciones de los circuitos perisilvianos que sustentan los mecanismos de lectura. Los estudios sobre TDAH sugieren una disfunción frontoestriatal ligada a las dificultades para el control inhibitorio, así como alteraciones en la corteza
temporal posterior y parietal inferior. Conclusiones. Los estudios de neuroimagen funcional revelan que las manifestaciones clínicas de estos trastornos no se deben sólo a la disfunción de áreas cerebrales concretas, sino también a alteraciones en el patrón de conectividadAs dificuldades de aprendizagem compreendem um grupo heterogéneo de perturbações que implicam alterações significativas em diferentes domínios cognitivos (aquisição e uso da linguagem, raciocínio, habilidades matemáticas, visuo-espaciais,
etc.) não justificadas por baixo nível intelectual, desenvolvimento sócio-cultural inadequado ou falta de oportunidades académicas. Estas são o resultado de uma alteração nos processos psicológicos básicos, evolutivamente ligados a uma alteração do sistema
nervoso central. As técnicas actuais de neuroimagem funcional permitiram um novo tipo de abordagem às bases neuro-funcionais destas perturbações, particularmente das dificuldades no âmbito da leitura e da escrita (dislexia evolutiva) e da perturbação por défice de atenção e hiperactividade (PDAH), as quais têm o maior nível de incidência na população escolar infantil. Desenvolvimento. Os estudos das neuroimagens revelaram um padrão de actividade atípico em ambos os tipos de perturbação. No caso da dislexia,
foram observadas alterações dos circuitos perisilvícos que sustentam os mecanismos de leitura. Os estudos sobre o PDAH sugerem uma disfunção fronto-estriatal ligada às dificuldades no controlo inibitório, assim como alterações no córtex temporal posterior
e parietal inferior. Conclusões. Os estudos de neuroimagem funcional revelam que as manifestações clínicas destas perturbações não se devem apenas à disfunção de áreas cerebrais concretas, como também a alterações no padrão de conectividad
Steady-State Visual Evoked Potentials Can Be Explained by Temporal Superposition of Transient Event-Related Responses
<p><b>Background:</b> One common criterion for classifying electrophysiological brain responses is based on the distinction between transient (i.e. event-related potentials, ERPs) and steady-state responses (SSRs). The generation of SSRs is usually attributed to the entrainment of a neural rhythm driven by the stimulus train. However, a more parsimonious account suggests that SSRs might result from the linear addition of the transient responses elicited by each stimulus. This study aimed to investigate this possibility.</p>
<p><b>Methodology/Principal Findings::</b> We recorded brain potentials elicited by a checkerboard stimulus reversing at different rates. We modeled SSRs by sequentially shifting and linearly adding rate-specific ERPs. Our results show a strong resemblance between recorded and synthetic SSRs, supporting the superposition hypothesis. Furthermore, we did not find evidence of entrainment of a neural oscillation at the stimulation frequency.</p>
<p><b>Conclusions/Significance:</b> This study provides evidence that visual SSRs can be explained as a superposition of transient ERPs. These findings have critical implications in our current understanding of brain oscillations. Contrary to the idea that neural networks can be tuned to a wide range of frequencies, our findings rather suggest that the oscillatory response of a given neural network is constrained within its natural frequency range.</p>
Revealing cell vulnerability in Alzheimer's disease by single-cell transcriptomics
Acord transformatiu CRUE-CSICAlzheimer's disease (AD) is a neurodegenerative disorder that by affecting specific brain cell types and regions cause severe pathological and functional changes in memory neural circuits. A comprehensive knowledge of the pathogenic mechanisms underlying AD requires a deeper understanding of the cell-specific pathological responses through integrative molecular analyses. Recent application of high-throughput single-cell transcriptomics to postmortem tissue has proved powerful to unravel cell susceptibility and biological networks responding to amyloid and tau pathologies. Here, we review single-cell transcriptomic studies successfully applied to decipher cell-specific gene expression programs and pathways in the brain of AD patients. Transcriptional information reveals both specific and common gene signatures affecting the major cerebral cell types, including astrocytes, endothelial cells, microglia, neurons, and oligodendrocytes. Cell type-specific transcriptomes associated with AD pathology and clinical symptoms are related to common biological networks affecting, among others pathways, synaptic function, inflammation, proteostasis, cell death, oxidative stress, and myelination. The general picture that emerges from systems-level single-cell transcriptomics is a spatiotemporal pattern of cell diversity and biological pathways, and novel cell subpopulations affected in AD brain. We argue that broader implementation of cell transcriptomics in larger AD human cohorts using standardized protocols is fundamental for reliable assessment of temporal and regional cell-type gene profiling. The possibility of applying this methodology for personalized medicine in clinics is still challenging but opens new roads for future diagnosis and treatment in dementia
Marked long-term decline in ambient CO mixing ratio in SE England, 1997–2014:Evidence of policy success in improving air quality
Atmospheric CO at Egham in SE England has shown a marked and progressive decline since 1997, following adoption of strict controls on emissions. The Egham site is uniquely positioned to allow both assessment and comparison of ‘clean Atlantic background’ air and CO-enriched air downwind from the London conurbation. The decline is strongest (approximately 50ppb per year) in the 1997–2003 period but continues post 2003. A ‘local CO increment’ can be identified as the residual after subtraction of contemporary background Atlantic CO mixing ratios from measured values at Egham. This increment, which is primarily from regional sources (during anticyclonic or northerly winds) or from the European continent (with easterly air mass origins), has significant seasonality, but overall has declined steadily since 1997. On many days of the year CO measured at Egham is now not far above Atlantic background levels measured at Mace Head (Ireland). The results are consistent with MOPITT satellite observations and ‘bottom-up’ inventory results. Comparison with urban and regional background CO mixing ratios in Hong Kong demonstrates the importance of regional, as opposed to local reduction of CO emission. The Egham record implies that controls on emissions subsequent to legislation have been extremely successful in the UK
Genetic analyses of celiac disease in a Spanish population confirm association with CELIAC3 but not with CELIAC4
[EN] Genetic predisposition to celiac disease (CD) is determined primarily by the human leukocyte antigen (HLA) genes (CELIAC1 region; 6p21), although many loci are involved in disease susceptibility. First, we have analysed a large series of CD patients from the Spanish Mediterranean region who had previously been characterised for the HLA complex. We have investigated how relevant regions contribute to CD susceptibility: CELIAC3 (CD28/CTLA4/ICOS region on 2q33) and CELIAC4 (19p13) as well as the tumour necrosis factor alpha (TNF-alpha) and the linfotoxin loci by case-control and association analyses. We highlight the association with the +49*A allele of cytotoxic T-lymphocyte-associated antigen 4 locus (P = 0.01), and the -308*A of TNF-alpha locus (P = 0.0008) in DQ2 individuals, although an independent role for TNF-alpha as risk factor has not been proven. Moreover, we do not confirm the association with the CELIAC4 region polymorphisms described in other populations.We are grateful for the kind collaboration of patients and families and Asociación de Celíacos de la Comunidad Valenciana (ACECOVA). This work was supported by the Fondo de Investigacio¿n Sanitaria (grant PI02573) and by the CSIC Intramural Frontiers Project (PROFICEL). ED holds a fellowship from the Fundacio¿n La Fe. English text revised by F. BarracloughCapilla, A.; Donat, E.; Planelles, D.; Espinós-Armero, CÁ.; Ribes-Koninckx, C.; Palau, F. (2007). Genetic analyses of celiac disease in a Spanish population confirm association with CELIAC3 but not with CELIAC4. Tissue Antigens. 70(4):324-329. https://doi.org/10.1111/j.1399-0039.2007.00899.x32432970
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