39 research outputs found

    The mutational impact of culturing human pluripotent and adult stem cells

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    Genetic changes acquired during in vitro culture pose a risk for the successful application of stem cells in regenerative medicine. To assess the genetic risks induced by culturing, we determined all mutations in individual human stem cells by whole genome sequencing. Individual pluripotent, intestinal, and liver stem cells accumulate 3.5 ± 0.5, 7.2 ± 1.1 and 8.3 ± 3.6 base substitutions per population doubling, respectively. The annual in vitro mutation accumulation rate of adult stem cells is nearly 40-fold higher than the in vivo mutation accumulation rate. Mutational signature analysis reveals that in vitro induced mutations are caused by oxidative stress. Reducing oxygen tension in culture lowers the mutational load. We use the mutation rates, spectra, and genomic distribution to model the accumulation of oncogenic mutations during typical in vitro expansion, manipulation or screening experiments using human stem cells. Our study provides empirically defined parameters to assess the mutational risk of stem cell based therapies

    Photochemical activation of TRPA1 channels in neurons and animals

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    Optogenetics is a powerful research tool because it enables high-resolution optical control of neuronal activity. However, current optogenetic approaches are limited to transgenic systems expressing microbial opsins and other exogenous photoreceptors. Here, we identify optovin, a small molecule that enables repeated photoactivation of motor behaviors in wild type animals. Surprisingly, optovin's behavioral effects are not visually mediated. Rather, photodetection is performed by sensory neurons expressing the cation channel TRPA1. TRPA1 is both necessary and sufficient for the optovin response. Optovin activates human TRPA1 via structure-dependent photochemical reactions with redox-sensitive cysteine residues. In animals with severed spinal cords, optovin treatment enables control of motor activity in the paralyzed extremities by localized illumination. These studies identify a light-based strategy for controlling endogenous TRPA1 receptors in vivo, with potential clinical and research applications in non-transgenic animals, including humans

    Present state and future perspectives of using pluripotent stem cells in toxicology research

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    The use of novel drugs and chemicals requires reliable data on their potential toxic effects on humans. Current test systems are mainly based on animals or in vitro–cultured animal-derived cells and do not or not sufficiently mirror the situation in humans. Therefore, in vitro models based on human pluripotent stem cells (hPSCs) have become an attractive alternative. The article summarizes the characteristics of pluripotent stem cells, including embryonic carcinoma and embryonic germ cells, and discusses the potential of pluripotent stem cells for safety pharmacology and toxicology. Special attention is directed to the potential application of embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) for the assessment of developmental toxicology as well as cardio- and hepatotoxicology. With respect to embryotoxicology, recent achievements of the embryonic stem cell test (EST) are described and current limitations as well as prospects of embryotoxicity studies using pluripotent stem cells are discussed. Furthermore, recent efforts to establish hPSC-based cell models for testing cardio- and hepatotoxicity are presented. In this context, methods for differentiation and selection of cardiac and hepatic cells from hPSCs are summarized, requirements and implications with respect to the use of these cells in safety pharmacology and toxicology are presented, and future challenges and perspectives of using hPSCs are discussed

    Alloplastische Implantate in der Kopf- und Halschirurgie.

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    Cold-inducible proteins CIRP and RBM3, a unique couple with activities far beyond the cold

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    History of Teflon

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    Medical History of Teflon

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    Ecoalim: a dataset of the environmental impacts of feed ingredients used for animal production in France

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    Feeds contribute highly to the environmental impacts of livestock products. Therefore formulating low-impact feeds necessitates data of the environmental impacts of feed ingredients with consistent perimeters and methodology for life cycle assessment (LCA). We built the ECOALIM dataset of life cycle inventories (LCI) and associated impacts for feed ingredients utilised in animal production in France. It provides several perimeters for LCI (field gate, storage organization gate, plant gate and harbour gate) with homogeneous data source from R&D French institutes covering the period 2005-2012. The dataset of 149 environmental impacts is available as an Excel spreadsheet on the ECOALIM website and provides ILCD and CML climate change and acidification, eutrophication, CED non-renewable energy, phosphorus consumption, and CML land occupation. Life cycle inventories of the ECOALIM dataset are available in the Agribalyse® database in SimaPro® software. The ECOALIM dataset can be utilized by the feed manufacturer and the LCA practitioner to investigate the formulation of low-impact feeds. It also provides data for environmental evaluation of feeds and environmental evaluation of animal production systems
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