Rainbow trout slow myoblast cell culture as a model to study slow skeletal muscle, and the characterization of mir-133 and mir-499 families as a case study

被引:17
作者
da Silva Duran, Bruno Oliveira [1 ]
Dal-Pai-Silva, Maeli [1 ]
Garcia de la Serrana, Daniel [2 ,3 ]
机构
[1] Sao Paulo State Univ UNESP, Inst Biosci, Dept Morphol, BR-18618689 Botucatu, SP, Brazil
[2] Univ St Andrews, Sch Biol, Scottish Oceans Inst, St Andrews KY16 8LB, Fife, Scotland
[3] Univ Barcelona, Fac Biol, Dept Cell Biol Physiol & Immunol, Barcelona 08028, Spain
基金
巴西圣保罗研究基金会;
关键词
Slow skeletal muscle; Cell culture; Myoblasts; miRNA; Electrostimulation; GILTHEAD SEA BREAM; RECEPTOR SIGNAL-TRANSDUCTION; IGF-I BINDING; GENE-EXPRESSION; GENOME DUPLICATION; REGULATORY FACTORS; SATELLITE CELLS; MYOMIR NETWORK; FIBER TYPES; INSULIN;
D O I
10.1242/jeb.216390
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Muscle fibres are classified as fast, intermediate and slow. In vitro myoblast cell culture model from fast muscle is a very useful tool to study muscle growth and development; however, similar models for slow muscle do not exist. Owing to the compartmentalization of fish muscle fibres, we have developed a slow myoblast cell culture for rainbow trout (Oncorhynchus mykiss). Slow and fast muscle-derived myoblasts have similar morphology, but with differential expression of slow muscle markers such as slow myhc, sox6 and pgc-1a. We also characterized the mir-133 and mir-499 microRNA families in trout slow and fast myoblasts as a case study during myogenesis and in response to electrostimulation. Three mir-133 (a-1a, a-1b and a-2) and four mir-499 (aa, ab, ba and bb) paralogues were identified for rainbow trout and named base on their phylogenetic relationship to zebrafish and Atlantic salmon orthologues. Omy-mir-499ab and omy-mir-499bb had 0.6 and 0.5-fold higher expression in slow myoblasts compared with fast myoblasts, whereas mir-133 duplicates had similar levels in both phenotypes and little variation during development. Slow myoblasts also showed increased expression for omy-mir-499b paralogues in response to chronic electrostimulation (7-fold increase for omy-mir-499ba and 2.5-fold increase for omy-mir-499bb). The higher expression of mir-499 paralogues in slow myoblasts suggests a role in phenotype determination, while the lack of significant differences of mir-133 copies during culture development might indicate a different role in fish compared with mammals. We have also found signs of sub-functionalization of mir-499 paralogues after electrostimulation, with omy-mir-499b copies more responsive to electrical signals.
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页数:12
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