‘’I hvilken grad kan fysisk aktivitet føre til et opplevd lavere nivå av stress i hverdagen?’’

Bakgrunn: Alle mennesker opplever en eller annen form for stress i hverdagen, noen mer enn andre. I enkelte situasjoner kan stress virke på en positiv måte, men som oftest er det en negativ side ved det. Hensikten med denne oppgaven er å finne, vurdere og evaluere relevante studier om fysisk aktivitet og stress. Problemstilling: I hvilken grad kan fysisk aktivitet føre til et opplevd lavere nivå av stress i hverdagen? Metode: Oppgaven er en litteraturstudie der det er utført et systematisk litteratursøk i MEDLINE og PsycINFO. Det ble plukket ut syv relevante artikler som sto i samspill med problemstillingen. Resultater: Oppgaven har tatt for seg syv studier og vurdert resultatene. Tre av hovedstudiene i denne oppgaven fant en signifikant reduksjon i opplevelsen av stress. De resterende fire fant ingen forskjell. Tre av fire studier som ikke fant noen forskjell hadde lav utvalgsstørrelse, der igjen to av disse hadde en testperiode som var for kort. Studiene viser stor spredning i resultatene og det er derfor behov for mer forskning for å kunne konkludere med en sikker sammenheng. Konklusjon: På tre av syv studier som har blitt vurdert, viser resultatet at fysisk aktivitet kan redusere opplevelsen av stress. Det er i midlertidig ikke enighet i resultatene hos de ulike studiene, og av den grunn trengs det derfor mer forskning og økt kunnskap i sammenhengen mellom fysisk aktivitet og opplevelsen av stress før man kan konkludere

Effect of ultrasonic cavitation on small and large organisms for water disinfection during fish transport

Motivated by the need for additional tools to disinfect discharge water from well boats, and to prevent distribution of salmon lice, the effect of ultrasonic cavitation on the planktonic stages of the salmon louse, nauplii and copepodids, as well as marine heterotrophic bacteria, and the marine green microalgae Tetraselmis suecica, has been investigated. Survival and morphology were registered after different exposure times. Efficacy of the ultrasonic cavitation treatments varied with exposure time. A reduction in survival was registered even for the shortest exposure time (5 seconds) for both naupliar and copepodid stages of the salmon louse (36.7 ± 11.5 and 67.20 ± 7.2% survival respectively). Survival reached zero after exposure times of 20 and 60 seconds for the nauplii and copepodid stages, respectively. A reduction in 70% was observed for bacteria at all exposure times (5 to 300 s), while a reduction of 95% was observed after 300 s for algal cells. The logged energy transfer to the samples was on average 17.5 J/s. In conclusion, cavitation treatment is destructive for the planktonic stages of salmon lice, and may contribute to reduce discharge of pathogens and parasites from well boats when adapted for this purpose and combined with existing water disinfection methods.publishedVersio

Software product line engineering: a practical experience

The lack of mature tool support is one of the main reasons that make the industry to be reluctant to adopt Software Product Line (SPL) approaches. A number of systematic literature reviews exist that identify the main characteristics offered by existing tools and the SPL phases in which they can be applied. However, these reviews do not really help to understand if those tools are offering what is really needed to apply SPLs to complex projects. These studies are mainly based on information extracted from the tool documentation or published papers. In this paper, we follow a different approach, in which we firstly identify those characteristics that are currently essential for the development of an SPL, and secondly analyze whether the tools provide or not support for those characteristics. We focus on those tools that satisfy certain selection criteria (e.g., they can be downloaded and are ready to be used). The paper presents a state of practice with the availability and usability of the existing tools for SPL, and defines different roadmaps that allow carrying out a complete SPL process with the existing tool support.Universidad de Málaga. Campus de Excelencia Internacional Andalucía Tech. Magic P12-TIC1814, HADAS TIN2015-64841-R (cofinanciado con fondos FEDER), MEDEA RTI2018-099213-B-I00 (cofinanciado con fondos FEDER), TASOVA MCIU-AEI TIN2017-90644-RED

Taz protects hematopoietic stem cells from an aging-dependent decrease in PU.1 activity

Specific functions of the immune system are essential to protect us from infections caused by pathogens such as viruses and bacteria. However, as we age, the immune system shows a functional decline that can be attributed in large part to age-associated defects in hematopoietic stem cells (HSCs)-the cells at the apex of the immune cell hierarchy. Here, we find that the Hippo pathway coactivator TAZ is potently induced in old HSCs and protects these cells from functional decline. We identify Clca3a1 as a TAZ-induced gene that allows us to trace TAZ activity in vivo. Using CLCA3A1 as a marker, we can isolate "young-like" HSCs from old mice. Mechanistically, Taz acts as coactivator of PU.1 and to some extent counteracts the gradual loss of PU.1 expression during HSC aging. Our work thus uncovers an essential role for Taz in a previously undescribed fail-safe mechanism in aging HSCs. Immune system function declines with age, a consequence of defects in hematopoietic stem cells (HSCs). Here the authors show that TAZ buffers age-related loss of PU.1 activity to maintain HSC functionality and identify the surface protein Clca3a1 as a marker of "young-like" HSCs, even in old mice

Human organotypic airway and lung organoid cells of bronchiolar and alveolar differentiation are permissive to infection by influenza and SARS-CoV-2 respiratory virus

The ongoing coronavirus disease 2019 (COVID-19) pandemic has led to the initiation of unprecedented research efforts to understand the pathogenesis mediated by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). More knowledge is needed regarding the cell type-specific cytopathology and its impact on cellular tropism. Furthermore, the impact of novel SARS-CoV-2 mutations on cellular tropism, alternative routes of entry, the impact of co-infections, and virus replication kinetics along the respiratory tract remains to be explored in improved models. Most applied virology models are not well suited to address the remaining questions, as they do not recapitulate the histoarchitecture and cellular composition of human respiratory tissues. The overall aim of this work was to establish from single biopsy specimens, a human adult stem cell-derived organoid model representing the upper respiratory airways and lungs and explore the applicability of this model to study respiratory virus infection. First, we characterized the organoid model with respect to growth pattern and histoarchitecture, cellular composition, and functional characteristics. Next, in situ expression of viral entry receptors, including influenza virus-relevant sialic acids and SARS-CoV-2 entry receptor ACE2 and TMPRSS2, were confirmed in organoids of bronchiolar and alveolar differentiation. We further showed successful infection by pseudotype influenza A H7N1 and H5N1 virus, and the ability of the model to support viral replication of influenza A H7N1 virus. Finally, successful infection and replication of a clinical isolate of SARS-CoV-2 were confirmed in the organoids by TCID50 assay and immunostaining to detect intracellular SARS-CoV-2 specific nucleocapsid and dsRNA. The prominent syncytia formation in organoid tissues following SARS-CoV-2 infection mimics the findings from infected human tissues in situ. We conclude that the human organotypic model described here may be particularly useful for virology studies to evaluate regional differences in the host response to infection. The model contains the various cell types along the respiratory tract, expresses respiratory virus entry factors, and supports successful infection and replication of influenza virus and SARS-CoV-2. Thus, the model may serve as a relevant and reliable tool in virology and aid in pandemic preparedness, and efficient evaluation of antiviral strategies.publishedVersio

Genome-Wide Gene Amplification during Differentiation of Neural Progenitor Cells In Vitro

DNA sequence amplification is a phenomenon that occurs predictably at defined stages during normal development in some organisms. Developmental gene amplification was first described in amphibians during gametogenesis and has not yet been described in humans. To date gene amplification in humans is a hallmark of many tumors. We used array-CGH (comparative genomic hybridization) and FISH (fluorescence in situ hybridization) to discover gene amplifications during in vitro differentiation of human neural progenitor cells. Here we report a complex gene amplification pattern two and five days after induction of differentiation of human neural progenitor cells. We identified several amplified genes in neural progenitor cells that are known to be amplified in malignant tumors. There is also a striking overlap of amplified chromosomal regions between differentiating neural progenitor cells and malignant tumor cells derived from astrocytes. Gene amplifications in normal human cells as physiological process has not been reported yet and may bear resemblance to developmental gene amplifications in amphibians and insects

Harmonising knowledge for safer materials via the “NanoCommons” Knowledge Base

In mediaeval Europe, the term “commons” described the way that communities managed land that was held “in common” and provided a clear set of rules for how this “common land” was used and developed by, and for, the community. Similarly, as we move towards an increasingly knowledge-based society where data is the new oil, new approaches to sharing and jointly owning publicly funded research data are needed to maximise its added value. Such common management approaches will extend the data’s useful life and facilitate its reuse for a range of additional purposes, from modelling, to meta-analysis to regulatory risk assessment as examples relevant to nanosafety data. This “commons” approach to nanosafety data and nanoinformatics infrastructure provision, co-development, and maintenance is at the heart of the “NanoCommons” project and underpins its post-funding transition to providing a basis on which other initiatives and projects can build. The present paper summarises part of the NanoCommons infrastructure called the NanoCommons Knowledge Base. It provides interoperability for nanosafety data sources and tools, on both semantic and technical levels. The NanoCommons Knowledge Base connects knowledge and provides both programmatic (via an Application Programming Interface) and a user-friendly graphical interface to enable (and democratise) access to state of the art tools for nanomaterials safety prediction, NMs design for safety and sustainability, and NMs risk assessment, as well. In addition, the standards and interfaces for interoperability, e.g., file templates to contribute data to the NanoCommons, are described, and a snapshot of the range and breadth of nanoinformatics tools and models that have already been integrated are presented Finally, we demonstrate how the NanoCommons Knowledge Base can support users in the FAIRification of their experimental workflows and how the NanoCommons Knowledge Base itself has progressed towards richer compliance with the FAIR principles