Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing, China.
Cell Prolif. 2010 Apr;43(2):157-63. doi: 10.1111/j.1365-2184.2010.00666.x.
We needed to establish an embryonic fibroblast cell line from the Langshan chicken (LSCEF61) to preserve their important genetic resources at the cellular level.
The cell line was established from 9-day-old embryos by direct explant culture and cryopreservation techniques. Cell morphology, dynamic proliferation and any contamination present were tested, and the karyotype and levels of isoenzymes of lactic dehydrogenase and malic dehydrogenase were analysed. Four types of fluorescent protein exogenous genes for pEGFP-C(1), pEGFP-N(3), pEYFP-N(1) and pDsRed1-N(1) were transfected into the cells.
Showed that the cells were healthy and were of spindle shaped structure, without change in morphology. Cell growth curves were of typical S-shape. Assays for microbial contamination were negative. The LSCEF61 line showed no cross-contamination when assessed by isoenzyme analysis. Chromosome number (2n) = 78 on more than 90% of occasions. The four types of fluorescent protein extro-genes appeared to be expressed effectively with high transfection efficiency between 15.6% and 38.6%.
The cell line met each of the quality control standards required for the American Type Culture Collection. It had not only preserved the genetic resources of the important Langshan chicken at the cellular level, but also provided valuable material for genomic, post-genomic and somatic cell cloning research and other applications.
我们需要建立一个来自郎山鸡(LSCEF61)的胚胎成纤维细胞系,以在细胞水平上保存它们重要的遗传资源。
通过直接组织块培养和冷冻保存技术,从 9 日龄胚胎中建立细胞系。测试细胞形态、动态增殖和任何存在的污染,并分析其核型和乳酸脱氢酶和苹果酸脱氢酶同工酶的水平。将四种类型的荧光蛋白外源性基因 pEGFP-C(1)、pEGFP-N(3)、pEYFP-N(1)和 pDsRed1-N(1)转染到细胞中。
表明细胞健康,呈纺锤形结构,形态无变化。细胞生长曲线呈典型的 S 形。微生物污染检测呈阴性。同工酶分析表明,LSCEF61 系没有交叉污染。染色体数(2n)在 90%以上的情况下为 78 条。四种类型的荧光蛋白外显子基因表达有效,转染效率在 15.6%至 38.6%之间。
该细胞系符合美国典型培养物保藏中心的质量控制标准。它不仅在细胞水平上保存了郎山鸡重要的遗传资源,还为基因组、后基因组和体细胞核克隆研究及其他应用提供了有价值的材料。