Establishment, characterization of a new cell line from heart of half smooth tongue sole (Cynoglossus semilaevis).

X L Wang, N Wang, Z X Sha, S L Chen
Author Information
  1. X L Wang: Key Lab for Sustainable Utilization of Marine Fisheries Resources, Ministry of Agriculture, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Nanjing Road 106, 266071, Qingdao, China.

Abstract

A new cell line was established from the heart of a cultured marine fish, half smooth tongue sole (Cynoglossus semilaevis), designated as CSH (Cynoglossus semilaevis heart cell line). The CSH cells grow over 400 days in minimum essential medium (MEM) supplemented with 10% fetal bovine serum (FBS) and 2 ng/ml basic fibroblast growth factor (bFGF). The suitable temperature for the cell growth was 24-30°C with the optimum growth at 24°C and a reduced growth at 12 and 30°C. FBS and bFGF concentration were the two important components for CSH cells proliferation. Twenty percent FBS in the medium was found to be the optimum concentration and bFGF promoted the growth of CSH cells. The double time of the cells at 24°C was determined to 73.39 h. Chromosome analysis revealed that 44% of the cells maintained a normal diploid chromosome number (2n=42) in the CSH cells at Passage 58. The fluorescent signals were observed in CSH after the cells were transfected with green fluorescent protein (GFP) reporter plasmids. CSH cells showed the cytopathic effect (CPE) after infection with lymphosystis disease virus (LCDV). Moreover, the LCDV particles can be observed in the cytoplasm of virus-infected cells by electron microscopy, and a segment of MCP gene for major capsid protein of LCDV was found by PCR amplification DNA of virus-infected cells.

References

  1. J Cell Biol. 1988 Oct;107(4):1611-9 [PMID: 2459134]
  2. In Vitro Cell Dev Biol Anim. 2009 Mar-Apr;45(3-4):127-34 [PMID: 19184248]
  3. J Exp Zool. 1988 Dec;248(3):290-302 [PMID: 3062124]
  4. Mar Biotechnol (NY). 2007 May-Jun;9(3):370-6 [PMID: 17342554]
  5. Dis Aquat Organ. 2004 Sep 8;60(3):241-6 [PMID: 15521323]
  6. Mol Mar Biol Biotechnol. 1994 Apr;3(2):78-86 [PMID: 8087186]
  7. Ann N Y Acad Sci. 1965 Aug 10;126(1):362-74 [PMID: 4957056]
  8. Mar Biotechnol (NY). 2007 Jan-Feb;9(1):82-91 [PMID: 17136469]
  9. Mar Biotechnol (NY). 2005 Jul-Aug;7(4):389-95 [PMID: 15976938]
  10. Cell. 1992 Sep 4;70(5):841-7 [PMID: 1381289]
  11. Toxicol In Vitro. 1991;5(1):91-100 [PMID: 20732002]
  12. Mar Biotechnol (NY). 2007 Nov-Dec;9(6):766-75 [PMID: 17704967]
  13. Mar Biotechnol (NY). 2007 Mar-Apr;9(2):281-91 [PMID: 17216384]

MeSH Term

Animals
Capsid Proteins
Cell Line
Culture Media
Cytogenetic Analysis
DNA Primers
Flatfishes
Green Fluorescent Proteins
Iridoviridae
Microscopy, Electron
Myocytes, Cardiac
Plasmids
Polymerase Chain Reaction
Temperature

Chemicals

Capsid Proteins
Culture Media
DNA Primers
Green Fluorescent Proteins

Word Cloud

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