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

Fish Physiol Biochem. 2010 Dec;36(4):1181-9. doi: 10.1007/s10695-010-9396-5. Epub 2010 Apr 8.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Capsid Proteins / genetics
  • Cell Line*
  • Culture Media
  • Cytogenetic Analysis
  • DNA Primers / genetics
  • Flatfishes*
  • Green Fluorescent Proteins / metabolism
  • Iridoviridae / genetics
  • Iridoviridae / ultrastructure
  • Microscopy, Electron
  • Myocytes, Cardiac / cytology*
  • Myocytes, Cardiac / virology
  • Plasmids / genetics
  • Polymerase Chain Reaction
  • Temperature

Substances

  • Capsid Proteins
  • Culture Media
  • DNA Primers
  • Green Fluorescent Proteins