Telomerase Activity and Myogenesis Ability as an Indicator of Cultured Turkey Satellite Cell Ability for In Vitro Meat Production

Q4 Biochemistry, Genetics and Molecular Biology Medical Journal of Cell Biology Pub Date : 2021-03-01 DOI:10.2478/acb-2021-0004
A. G. Narenji, J. Petitte, M. Kulus, K. Stefańska, Joanna Perek, Jakub Kulus, M. Wieczorkiewicz, M. Jankowski, A. Bryja, Rut Bryl, P. Antosik, D. Bukowska, Jędrzej M. Jaśkowki, Kornel Ratajczak, P. Mozdziak
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引用次数: 2

Abstract

Abstract Telomerase activity is highly correlated to the proliferation capacity and immortality of cells. To evaluate the possibility of continuous culture, myoblasts were isolated from the Pectoralis thoracicus muscle of newborn turkeys and maintained in 2D (adherence based) and suspension cultures. Furthermore, adherent myoblasts were differentiated into myotubes. Telomerase activity was evaluated in all types of obtained cultures. The expression of telomerase related genes, including TERT1, TERT2, dyskerin, as well as myogenesis related genes, including myogenin, MyoD, MRF1 and MRF5 were measured. Telomerase bands were detected in both adherent and suspended cells, but they were not detected in samples from rat muscle. Myotube differentiation caused a significant reduction in the expression of TERT1, TERT2 and Dyskerin, while MyoD, Myogenin and MRF4 were upregulated in myotubes vs. myoblasts. Long-term culture of suspended myoblasts caused a significant increase in TERT1 levels, with no significant change in expression of myogenesis related genes. Overall, the results show that myoblasts are able to grow in suspension without losing their myogenic properties. Furthermore, upregulation of TERT1 indicates continued proliferation of myoblasts and generation of enough daughter cells necessary for in vitro meat production. Running title: Telomerase activity and myogenic properties of cultured Turkey satellite cells
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端粒酶活性和肌肉发生能力作为体外培养火鸡卫星细胞产肉能力的指标
端粒酶活性与细胞的增殖能力和长生不老密切相关。为了评估连续培养的可能性,从新生火鸡的胸胸肌中分离出成肌细胞,并在2D(粘附性)和悬浮培养中维持。贴壁成肌细胞分化为肌管。在获得的所有类型的培养物中评估端粒酶活性。检测端粒酶相关基因TERT1、TERT2、dyskerin的表达,以及肌生成相关基因myogenin、MyoD、MRF1、MRF5的表达。在贴壁细胞和悬浮细胞中均检测到端粒酶条带,但在大鼠肌肉样品中未检测到端粒酶条带。肌管分化导致TERT1、TERT2和Dyskerin的表达显著降低,而MyoD、Myogenin和MRF4在肌管中与成肌细胞相比表达上调。悬浮成肌细胞长期培养,TERT1水平显著升高,而肌生成相关基因表达无明显变化。总的来说,结果表明成肌细胞能够在悬浮液中生长而不失去其成肌特性。此外,TERT1的上调表明成肌细胞的持续增殖和产生足够的子细胞,这是体外肉生产所必需的。运行标题:端粒酶活性和培养的土耳其卫星细胞的成肌特性
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来源期刊
Medical Journal of Cell Biology
Medical Journal of Cell Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
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