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      The effect of temperature on proliferation and differentiation of chicken skeletal muscle satellite cells isolated from different muscle types

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          Abstract

          Skeletal muscle satellite cells are a muscle stem cell population that mediate posthatch muscle growth and repair. Satellite cells respond differentially to environmental stimuli based upon their fiber‐type of origin. The objective of this study was to determine how temperatures below and above the in vitro control of 38°C affected the proliferation and differentiation of satellite cells isolated from the chicken anaerobic pectoralis major (p. major) or mixed fiber biceps femoris (b.femoris) muscles. The satellite cells isolated from the p. major muscle were more sensitive to both cold and hot temperatures compared to the b.femoris satellite cells during both proliferation and differentiation. The expressions of myogenic regulatory transcription factors were also different between satellite cells from different fiber types. MyoD expression, which partially regulates proliferation, was generally expressed at higher levels in p. major satellite cells compared to the b.femoris satellite cells from 33 to 43°C during proliferation and differentiation. Similarly, myogenin expression, which is required for differentiation, was also expressed at higher levels in p. major satellite cells in response to both cold and hot temperatures during proliferation and differentiation than b. femoris satellite cells. These data demonstrate that satellite cells from the anaerobic p. major muscle are more sensitive than satellite cells from the aerobic b. femoris muscle to both hot and cold thermal stress during myogenic proliferation and differentiation.

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          Most cited references23

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          Myogenic satellite cells: physiology to molecular biology.

          Adult skeletal muscle has a remarkable ability to regenerate following myotrauma. Because adult myofibers are terminally differentiated, the regeneration of skeletal muscle is largely dependent on a small population of resident cells termed satellite cells. Although this population of cells was identified 40 years ago, little is known regarding the molecular phenotype or regulation of the satellite cell. The use of cell culture techniques and transgenic animal models has improved our understanding of this unique cell population; however, the capacity and potential of these cells remain ill-defined. This review will highlight the origin and unique markers of the satellite cell population, the regulation by growth factors, and the response to physiological and pathological stimuli. We conclude by highlighting the potential therapeutic uses of satellite cells and identifying future research goals for the study of satellite cell biology.
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            Mrf4 determines skeletal muscle identity in Myf5:Myod double-mutant mice.

            In vertebrates, skeletal muscle is a model for the acquisition of cell fate from stem cells. Two determination factors of the basic helix-loop-helix myogenic regulatory factor (MRF) family, Myf5 and Myod, are thought to direct this transition because double-mutant mice totally lack skeletal muscle fibres and myoblasts. In the absence of these factors, progenitor cells remain multipotent and can change their fate. Gene targeting studies have revealed hierarchical relationships between these and the other MRF genes, Mrf4 and myogenin, where the latter are regarded as differentiation genes. Here we show, using an allelic series of three Myf5 mutants that differentially affect the expression of the genetically linked Mrf4 gene, that skeletal muscle is present in the new Myf5:Myod double-null mice only when Mrf4 expression is not compromised. This finding contradicts the widely held view that myogenic identity is conferred solely by Myf5 and Myod, and identifies Mrf4 as a determination gene. We revise the epistatic relationship of the MRFs, in which both Myf5 and Mrf4 act upstream of Myod to direct embryonic multipotent cells into the myogenic lineage.
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              Skeletal muscle: energy metabolism, fiber types, fatigue and adaptability.

              Skeletal muscles cope with a large range of activities, from being able to support the body weight during long periods of upright standing to perform explosive movements in response to an unexpected threat. This requires systems for energy metabolism that can provide energy during long periods of moderately increased energy consumption as well as being able to rapidly increasing the rate of energy production more than 100-fold in response to explosive contractions. In this short review we discuss how muscles can deal with these divergent demands. We first outline the major energy metabolism pathways in skeletal muscle. Next we describe metabolic differences between different muscle fiber types. Contractile performance declines during intense activation, i.e. fatigue develops, and we discuss likely underlying mechanisms. Finally, we discuss the ability of muscle fibers to adapt to altered demands, and mechanisms behind these adaptations. The accumulated experimental evidence forces us to conclude that most aspects of energy metabolism involve multiple and overlapping signaling pathways, which indicates that the control of energy metabolism is too important to depend on one single molecule or mechanism. Copyright © 2010 Elsevier Inc. All rights reserved.
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                Author and article information

                Journal
                Physiol Rep
                Physiol Rep
                10.1002/(ISSN)2051-817X
                PHY2
                physreports
                Physiological Reports
                John Wiley and Sons Inc. (Hoboken )
                2051-817X
                28 April 2016
                April 2016
                : 4
                : 8 ( doiID: 10.1111/phy2.2016.4.issue-8 )
                : e12770
                Affiliations
                [ 1 ] Ohio Agricultural Research and Development CenterThe Ohio State University WoosterOhio
                [ 2 ] Department of Animal SciencesThe Hebrew University of Jerusalem RehovotIsrael
                [ 3 ] Institute of Animal SciencesAgricultural Research Organization The Volcani Center Bet DaganIsrael
                Author notes
                [*] [* ] Correspondence

                Sandra G. Velleman, The Ohio State University/OARDC, Department of Animal Sciences, 1680 Madison Ave., Wooster, OH 44691.

                Tel: 330‐263‐3905

                Fax: 330‐263‐3949

                E‐mail: Velleman.1@ 123456osu.edu

                Article
                PHY212770
                10.14814/phy2.12770
                4848725
                27125667
                4fd6d88b-601e-49e7-bf8d-628f2892c57f
                © 2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 09 February 2016
                : 24 March 2016
                : 31 March 2016
                Page count
                Pages: 13
                Funding
                Funded by: BARD
                Award ID: IS‐4592‐13
                Funded by: The United States‐Israel Binational Agricultural Research and Development Fund
                Categories
                Skeletal Muscle
                Thermoregulation
                Cellular Physiology
                Original Research
                Original Research
                Custom metadata
                2.0
                phy212770
                April 2016
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.9.1 mode:remove_FC converted:16.06.2016

                chicken,fiber type,muscle,satellite cells,temperature
                chicken, fiber type, muscle, satellite cells, temperature

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