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在体外成肌细胞发育和体内禁食期间,对真鲷(Sparus aurata)的成肌调节因子进行特征描述和表达分析。

Characterisation and expression of myogenesis regulatory factors during in vitro myoblast development and in vivo fasting in the gilthead sea bream (Sparus aurata).

机构信息

Departament de Fisiologia i Immunologia, Facultat de Biologia, Barcelona Knowledge Campus, Universitat de Barcelona, 08028, Barcelona, Spain; Scottish Oceans Institute, School of Biology, University of St Andrews, Fife KY16 8LB, St Andrews, Scotland, UK.

出版信息

Comp Biochem Physiol A Mol Integr Physiol. 2014 Jan;167:90-9. doi: 10.1016/j.cbpa.2013.10.020. Epub 2013 Oct 21.

DOI:10.1016/j.cbpa.2013.10.020
PMID:24157945
Abstract

The aim of this study was to characterise a primary cell culture isolated from fast skeletal muscle of the gilthead sea bream. Gene expression profiles during culture maturation were compared with those obtained from a fasting-refeeding model which is widely used to modulate myogenesis in vivo. Myogenesis is controlled by numerous extracellular signals together with intracellular transcriptional factors whose coordinated expression is critical for the appropriate development of muscle fibres. Full-length cDNAs for the transcription factors Myf5, Mrf4, Pax7 and Sox8 were cloned and sequenced for gilthead sea bream. Pax7, sox8, myod2 and myf5 levels were up-regulated during the proliferating phase of the myogenic cultures coincident with the highest expression of proliferating cell nuclear antigen (PCNA). In contrast, myogenin and mrf4 transcript abundance was highest during the differentiation phase of the culture when myotubes were present, and was correlated with increased myosin heavy chain (mhc) and desmin expression. In vivo, 30days of fasting resulted in muscle fibre atrophy, a reduction in myod2, myf5 and igf1 expression, lower number of Myod-positive cells, and decreased PCNA protein expression, whereas myogenin expression was not significantly affected. Myostatin1 (mstn1) and pax7 expression were up-regulated in fasted relative to well-fed individuals, consistent with a role for Pax7 in the reduction of myogenic cell activity with fasting. The primary cell cultures and fasting-feeding experiments described provide a foundation for the future investigations on the regulation of muscle growth in gilthead sea bream.

摘要

本研究旨在描述从金头鲷快速骨骼肌中分离出的原代细胞培养物。培养成熟过程中的基因表达谱与广泛用于体内调节肌生成的禁食-再喂养模型获得的表达谱进行了比较。肌生成受许多细胞外信号以及细胞内转录因子的控制,这些转录因子的协调表达对于肌肉纤维的适当发育至关重要。克隆并测序了金头鲷的转录因子 Myf5、Mrf4、Pax7 和 Sox8 的全长 cDNA。在肌生成培养物的增殖阶段,Pax7、sox8、myod2 和 myf5 的水平上调,与增殖细胞核抗原 (PCNA) 的最高表达一致。相比之下,myogenin 和 mrf4 的转录丰度在培养物的分化阶段最高,此时存在肌管,并且与肌球蛋白重链 (mhc) 和结蛋白表达的增加相关。在体内,30 天的禁食导致肌肉纤维萎缩,myod2、myf5 和 igf1 的表达减少,Myod 阳性细胞数量减少,PCNA 蛋白表达降低,而 myogenin 的表达没有明显变化。与饱食个体相比,fasting 状态下肌抑素 1 (mstn1) 和 pax7 的表达上调,这与 Pax7 在禁食时减少肌生成细胞活性的作用一致。所描述的原代细胞培养和禁食-喂养实验为未来研究金头鲷肌肉生长的调控提供了基础。

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