Establishment of Conditions for Long-Term Maintenance of Primary Embryonic Cell Cultures from Olive Flounder Paralichthys olivaceus.

Development & reproduction Pub Date : 2020-09-01 Epub Date: 2020-09-30 DOI:10.12717/DR.2020.24.3.207
Ju-Won Kim, Ja Young Cho, Dong-Gyun Kim, Bo-Hye Nam, Eun-Soo Nho, Bong-Seok Kim, Young-Ok Kim, Hee Jeong Kong
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引用次数: 3

Abstract

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 Paralichthys olivaceus 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.

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橄榄比目鱼胚胎细胞培养长期维持条件的建立。
原代细胞培养是一种在受控环境中研究分离细胞的细胞特性和机制的常用方法。本研究从橄榄比目鱼胚囊胚阶段发育了一株胚胎细胞系FGBC8。此外,研究了这种原代胚胎细胞培养的最佳长期维持条件。形态学上,FGBC8细胞主要由上皮样细胞组成。FGBC8细胞传代超过160代,约830天。FGBC8细胞加倍时间为73.8 h,双倍体染色体数为48条。转染绿色荧光蛋白(GFP)表达质粒的FGBC8细胞在转染48 h后表现出强信号。因此,我们证明了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。本研究结果可作为其他鱼类原代胚胎细胞培养的指导,并可用于细胞生物技术的应用。
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