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Comparison of growth characteristics between skeletal muscle satellite cell lines from diploid and triploid olive flounder Paralichthys olivaceus

Objectives. According to myosatellite cell lines (MSCs) established in vitro from diploid and triploid flounder, we compared the characters of growth and differentiation of their MSCs. The results would be useful for learning the muscle development mechanism in teleosts. Materials and Methods. The s...

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Detalles Bibliográficos
Autores principales: Peng, Li-min, Zheng, Yuan, You, Feng, Wu, Zhi-hao, Tan, Xungang, Jiao, Shuang, Zhang, Pei-jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4715439/
https://www.ncbi.nlm.nih.gov/pubmed/26788421
http://dx.doi.org/10.7717/peerj.1519
Descripción
Sumario:Objectives. According to myosatellite cell lines (MSCs) established in vitro from diploid and triploid flounder, we compared the characters of growth and differentiation of their MSCs. The results would be useful for learning the muscle development mechanism in teleosts. Materials and Methods. The skeletal muscle cells from the diploid and triploid olive flounder Paralichthys olivaceus were isolated and cultured in vitro, respectively, and the cells were characterized at the morphology and molecular level; meanwhile, the performance of these cells’ proliferation and differentiation were analyzed. Results. Two new skeletal muscle cell lines (POMSC(S(2n)) and POMSC(S(3n))) from diploid and triploid flounder have been respectively subcultured for 67 times and 66 times. The cultured cells were mostly spindle-like mononuclear cells. They have normal flounder diploid karyotype (2n=48t) and triploid karyotype (3n=72t), respectively. Muscle satellite cell gene marker (pax7b) and myogenic cell protein marker (Desmin) were all expressed in cells of two cell lines. Both of the cells could differentiate into the large polynucleated muscle fibre cells, and immunofluorescence reactions of myosin heavy chain (MyHC) were positive. There were more cells of POMSC(S(3n)) to differentiate into the muscle fibre cells than that of POMSC(S(2n)). However, POMSC(S(2n)) cells proliferated more rapidly than those of POMSC(S(3n)) (P < 0.05). The significant fluorescent signals were observed in both POMSC(S(2n)) and POMSC(S(3n)) cells after transfected with pEGFP-N3 reporter plasmid. Conclusions. The two cell lines have been established and characterized as MSCs. We suppose that it might be the differentiation capacity, rather than the proliferation activity of MSCs to play a key role in the better growth of triploid ones than diploid. Both cell lines will become the ideal tools to learn the mechanism of fish MSCs proliferation, differentiation and regeneration during muscle development in the future.