147 research outputs found

    Les matières picturales de la grotte d'Ekain (Pays Basque)

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    ‘Designing a wellbeing garden’ a systematic review of design recommendations

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    Evidence demonstrates the benefits of gardens for promoting wellbeing. Some gardens are now being designed specifically to promote wellbeing; however, there are currently no evidence-based guidelines or recommendations available for designers to support such endeavours. The present study undertakes a systematic review of garden design literature to: (1) identify the defining characteristics of a garden that promotes wellbeing in non-clinical populations; and (2) summarize existing evaluations of garden designs into recommendations that can promote wellbeing. Online databases were used to identify papers published before October 2022, from which 17 publications were reviewed. This review was conducted following PRISMA and framework for scoping reviews. Results: The defining characteristics of wellbeing gardens centred around six design aspects: accessibility, wayfinding, fostering serenity, multisensory planting, spatial organization, and cultural artefacts. From these, recommendations were developed for garden designers to create wellbeing gardens

    PIBF+ extracellular vesicles from mouse embryos affect IL-10 production by CD8+ cells

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    Earlier evidence suggests, that the embryo signals to the maternal immune system. Extracellular vesicles (EVs) are produced by all types of cells, and because they transport different kinds of molecules from one cell to the other, they can be considered as means of intercellular communication. The aim of this work was to test, whether the embryo is able to produce sufficient amounts of EVs to alter the function of peripheral lymphocytes. Embryo-derived EVs were identified by their Annexin V biding capacity, and sensitivity to Triton X dependent lysis, using flow cytometry. Transmission electron microscopy was used to detect EVs at the implantation site. Progesterone-induced blocking factor (PIBF) expression in embryo-derived EVs was demonstrated with immuno-electron microscopy. The % of IL-10 + murine lymphocytes was determined by flow cytometry. EVs were present in embryo culture media, but not in empty media. Mouse embryo-derived EVs adhere to the surface of both CD4+ and CD8+ murine peripheral T lymphocytes, partly, via phosphatidylserine binding. The number of IL-10+ murine peripheral CD8+ cells increases in the presence of embryo-derived EVS, and this effect is counteracted by pre-treatment of EVs with an anti-PIBF antibody, suggesting that the embryo communicates with the maternal immune system via EVs

    Low incidence of SARS-CoV-2, risk factors of mortality and the course of illness in the French national cohort of dialysis patients

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    Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018.

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    Over the past decade, the Nomenclature Committee on Cell Death (NCCD) has formulated guidelines for the definition and interpretation of cell death from morphological, biochemical, and functional perspectives. Since the field continues to expand and novel mechanisms that orchestrate multiple cell death pathways are unveiled, we propose an updated classification of cell death subroutines focusing on mechanistic and essential (as opposed to correlative and dispensable) aspects of the process. As we provide molecularly oriented definitions of terms including intrinsic apoptosis, extrinsic apoptosis, mitochondrial permeability transition (MPT)-driven necrosis, necroptosis, ferroptosis, pyroptosis, parthanatos, entotic cell death, NETotic cell death, lysosome-dependent cell death, autophagy-dependent cell death, immunogenic cell death, cellular senescence, and mitotic catastrophe, we discuss the utility of neologisms that refer to highly specialized instances of these processes. The mission of the NCCD is to provide a widely accepted nomenclature on cell death in support of the continued development of the field

    Exosome removal as a therapeutic adjuvant in cancer

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