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      Proteolysis inhibition by hibernating bear serum leads to increased protein content in human muscle cells

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          Abstract

          Muscle atrophy is one of the main characteristics of human ageing and physical inactivity, with resulting adverse health outcomes. To date, there are still no efficient therapeutic strategies for its prevention and/or treatment. However, during hibernation, bears exhibit a unique ability for preserving muscle in conditions where muscle atrophy would be expected in humans. Therefore, our objective was to determine whether there are components of bear serum which can control protein balance in human muscles. In this study, we exposed cultured human differentiated muscle cells to bear serum collected during winter and summer periods, and measured the impact on cell protein content and turnover. In addition, we explored the signalling pathways that control rates of protein synthesis and degradation. We show that the protein turnover of human myotubes is reduced when incubated with winter bear serum, with a dramatic inhibition of proteolysis involving both proteasomal and lysosomal systems, and resulting in an increase in muscle cell protein content. By modulating intracellular signalling pathways and inducing a protein sparing phenotype in human muscle cells, winter bear serum therefore holds potential for developing new tools to fight human muscle atrophy and related metabolic disorders.

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          SUnSET, a nonradioactive method to monitor protein synthesis.

          We developed a nonradioactive fluorescence-activated cell sorting-based assay, called surface sensing of translation (SUnSET), which allows the monitoring and quantification of global protein synthesis in individual mammalian cells and in heterogeneous cell populations. We demonstrate here, using mouse dendritic and T cells as a model, that SUnSET offers a technical alternative to classical radioactive labeling methods for the study of mRNA translation and cellular activation.
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            Signaling in muscle atrophy and hypertrophy.

            Muscle performance is influenced by turnover of contractile proteins. Production of new myofibrils and degradation of existing proteins is a delicate balance, which, depending on the condition, can promote muscle growth or loss. Protein synthesis and protein degradation are coordinately regulated by pathways that are influenced by mechanical stress, physical activity, availability of nutrients, and growth factors. Understanding the signaling that regulates muscle mass may provide potential therapeutic targets for the prevention and treatment of muscle wasting in metabolic and neuromuscular diseases.
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              Cellular and molecular mechanisms of muscle atrophy

              Skeletal muscle is a plastic organ that is maintained by multiple pathways regulating cell and protein turnover. During muscle atrophy, proteolytic systems are activated, and contractile proteins and organelles are removed, resulting in the shrinkage of muscle fibers. Excessive loss of muscle mass is associated with poor prognosis in several diseases, including myopathies and muscular dystrophies, as well as in systemic disorders such as cancer, diabetes, sepsis and heart failure. Muscle loss also occurs during aging. In this paper, we review the key mechanisms that regulate the turnover of contractile proteins and organelles in muscle tissue, and discuss how impairments in these mechanisms can contribute to muscle atrophy. We also discuss how protein synthesis and degradation are coordinately regulated by signaling pathways that are influenced by mechanical stress, physical activity, and the availability of nutrients and growth factors. Understanding how these pathways regulate muscle mass will provide new therapeutic targets for the prevention and treatment of muscle atrophy in metabolic and neuromuscular diseases.
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                Author and article information

                Contributors
                lefai@univ-lyon1.fr
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                3 April 2018
                3 April 2018
                2018
                : 8
                : 5525
                Affiliations
                [1 ]CarMeN Laboratory, INSERM, INRA, University of Lyon, Pierre-Benite, France
                [2 ]ISNI 0000 0001 2157 9291, GRID grid.11843.3f, Université de Strasbourg, CNRS, IPHC UMR 7178, ; F-67000 Strasbourg, France
                [3 ]Laboratoire de Spectrométrie de Masse Bio-Organique, 25 rue Becquerel, F-67087 Strasbourg, France
                [4 ]ISNI 0000 0001 2201 6490, GRID grid.13349.3c, Centre National d’Etudes Spatiales, CNES, ; 75039 Paris, France
                [5 ]Département Ecologie, Physiologie et Ethologie, 23 rue Becquerel, F-67087 Strasbourg, France
                [6 ]ISNI 0000 0001 2163 3825, GRID grid.413852.9, Department of digestive and bariatric surgery, Obesity Integrated Center, , University Hospital of Edouard Herriot, Hospices Civils de Lyon, Lyon 1 University, ; Lyon, France
                [7 ]ISNI 0000 0004 0607 975X, GRID grid.19477.3c, Faculty of Environmental Sciences and Natural Resource Management, , Norwegian University of Life Sciences, 1432, ; Ås, Norway
                [8 ]ISNI 0000 0001 2107 519X, GRID grid.420127.2, Norwegian Institute for Nature Research, ; 7485 Trondheim, Norway
                [9 ]GRID grid.463530.7, Department of Natural Sciences and Environmental Health, , University College of Southeast Norway, N3800 Bø in Telemark, ; Bø, Norway
                [10 ]ISNI 0000 0001 2298 5320, GRID grid.5173.0, Institute of Wildlife Biology and Game Management, , University of Natural Resources and Life Sciences, Vienna, Gregor Mendel Str. 33, ; A-1180 Vienna, Austria
                [11 ]GRID grid.477237.2, Department of Forestry and Wildlife Management, , Inland Norway University of Applied Sciences, ; NO-2480 Koppang, Norway
                [12 ]ISNI 0000 0000 8578 2742, GRID grid.6341.0, Department of Wildlife, Fish, and Environmental Studies, , Swedish University of Agricultural Sciences, ; SE-901 83 Umeå, Sweden
                [13 ]ISNI 0000 0004 1936 893X, GRID grid.34428.39, Institute of Biochemistry and Department of Biology, , Carleton University, 1125 Colonel By Drive, ; Ottawa, ON K1S 5B6 Canada
                Author information
                http://orcid.org/0000-0002-3042-7801
                Article
                23891
                10.1038/s41598-018-23891-5
                5883044
                29615761
                afd426a9-5906-45bf-b06a-0cd2f507dc62
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 29 December 2017
                : 21 March 2018
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