Kim Ju-Won, Cho Ja Young, Kim Dong-Gyun, Nam Bo-Hye, Nho Eun-Soo, Kim Bong-Seok, Kim Young-Ok, Kong Hee Jeong
Biotechnology Research Division, National Institute of Fisheries Science, Busan 46083, Korea.
Dev Reprod. 2020 Sep;24(3):207-214. doi: 10.12717/DR.2020.24.3.207. Epub 2020 Sep 30.
Primary cell culture is a sufficient method frequently used to study the cellular properties and mechanisms of isolated cells in a controlled environment. In this study, an embryonic cell line (FGBC8) derived from the blastula stages of embryos of olive flounder was developed. Furthermore, conditions for optimal long-term maintenance of this primary embryonic cell culture were investigated. Morphologically, FGBC8 cells were composed primarily of epithelial-like cells. FGBC8 cells were subcultured for >160 passages over ~830 days. The doubling time of FGBC8 cells was 73.8 h, and the modal diploid chromosome number was 48. FGBC8 cells transfected with green fluorescence protein (GFP)-expression plasmid exhibited a strong signal 48 h after transfection. Consequently, we demonstrated that fish serum is a crucial supplement for the long-term survival and maintenance of comparable morphology in these primary embryonic cells. Our results can be used as a guide for primary embryonic cell cultures for other fish species and may be useful for cell biotechnological applications.
原代细胞培养是一种常用的有效方法,用于在可控环境中研究分离细胞的细胞特性和机制。在本研究中,开发了一种源自牙鲆胚胎囊胚期的胚胎细胞系(FGBC8)。此外,还研究了该原代胚胎细胞培养的最佳长期维持条件。在形态上,FGBC8细胞主要由上皮样细胞组成。FGBC8细胞在约830天内传代超过160次。FGBC8细胞的倍增时间为73.8小时,核型二倍体染色体数为48条。用绿色荧光蛋白(GFP)表达质粒转染的FGBC8细胞在转染后48小时显示出强信号。因此,我们证明鱼血清是这些原代胚胎细胞长期存活和维持可比形态的关键补充物。我们的结果可为其他鱼类的原代胚胎细胞培养提供指导,并可能有助于细胞生物技术应用。