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

Author:

Peng Li-min123,Zheng Yuan12,You Feng12,Wu Zhi-hao12,Tan Xungang12,Jiao Shuang12,Zhang Pei-jun12

Affiliation:

1. Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao, China

2. Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China

3. University of Chinese Academy of Sciences, Beijing, China

Abstract

Objectives. According to myosatellite cell lines (MSCs) establishedin vitrofrom 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 flounderParalichthys olivaceuswere isolated and culturedin 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 (POMSCS(2n)and POMSCS(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 POMSCS(3n)to differentiate into the muscle fibre cells than that of POMSCS(2n). However, POMSCS(2n)cells proliferated more rapidly than those of POMSCS(3n)(P< 0.05). The significant fluorescent signals were observed in both POMSCS(2n)and POMSCS(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.

Funder

National High Technology Research and Development Program of China

National Natural Science Foundation of China

National Flatfish Industry System Construction Programme

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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