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Derivation and Characterization of a ES-Like Cell Line from Indian CatfishHeteropneustes fossilisBlastulas
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A cell line designated as HFB-ES was established from blastula stage embryos ofH. fossilis(Singhi). The embryonic cells were harvested and maintained in Leibovitz’s medium supplemented with 15% fetal bovine serum. The cell line had been subcultured for more than 90 passages in a period of 24 months. HFB-ES cells were able to grow at temperatures between 25 and 35°C with an optimum temperature of 28°C. The growth rate of HFB-ES was proportional to FBS concentration, with optimum growth seen at 15% FBS concentration. The originality of the cell line was confirmed by sequencing of cytochrome oxidase c subunit I (COI), cytochrome b gene, and microsatellite DNA profile. Results of chromosome complements of HFB showed normal karyo-morphology with 56 (2n) diploid number of chromosomes after 40 passages which indicated that the developed cell line is chromosomally stable. The pluripotency of HFB was demonstrated by alkaline phosphatase activity and Oct-4 gene expression. Expression of GFP reporter gene was successful in HFB-ES. These results indicated that HFB-ES could be utilized for future gene expression studies.
Title: Derivation and Characterization of a ES-Like Cell Line from Indian CatfishHeteropneustes fossilisBlastulas
Description:
A cell line designated as HFB-ES was established from blastula stage embryos ofH.
fossilis(Singhi).
The embryonic cells were harvested and maintained in Leibovitz’s medium supplemented with 15% fetal bovine serum.
The cell line had been subcultured for more than 90 passages in a period of 24 months.
HFB-ES cells were able to grow at temperatures between 25 and 35°C with an optimum temperature of 28°C.
The growth rate of HFB-ES was proportional to FBS concentration, with optimum growth seen at 15% FBS concentration.
The originality of the cell line was confirmed by sequencing of cytochrome oxidase c subunit I (COI), cytochrome b gene, and microsatellite DNA profile.
Results of chromosome complements of HFB showed normal karyo-morphology with 56 (2n) diploid number of chromosomes after 40 passages which indicated that the developed cell line is chromosomally stable.
The pluripotency of HFB was demonstrated by alkaline phosphatase activity and Oct-4 gene expression.
Expression of GFP reporter gene was successful in HFB-ES.
These results indicated that HFB-ES could be utilized for future gene expression studies.
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