Li Linfeng F, Guan Weijun J, Li Han, Zhou Xueyan Z, Bai Xiujuan J, Ma Yuehui H
Institute of Animal Science, Chinese Academy of Agricultural Science, Beijing, China.
Biochem Cell Biol. 2009 Jun;87(3):485-92. doi: 10.1139/o09-005.
A Texel sheep ear marginal tissue fibroblast cell line (named TSF19) was successfully established by using a primary explant technique and cell cryoconservation technology. TSF19 cells were adherent, with a population doubling time of 24.9 h. Chromosome analysis showed that >90% of cells were diploid prior to cell passage 4. Isoenzyme analyses of lactate dehydrogenase and malate dehydrogenase showed that the TSF19 cells had no cross-contamination with other species. Tests for cell line contamination with bacteria, fungi, or mycoplasmas were also negative. Plasmids encoding the fluorescent proteins pEGFP-N3, pECFP-N1, pDsRed1-N1, and pEYFP-N1 were transfected into cells to study exogenous gene expression in the cells. The plasmid transfection efficiency was between 21.8% and 46.5%. This newly established cell line will not only preserve the genetic resources of the important Texel sheep at the cell level but will also provide a valuable resource for genomic, postgenomic, somatic cloning research.
采用原代外植体技术和细胞冻存技术,成功建立了一种特克塞尔绵羊耳缘组织成纤维细胞系(命名为TSF19)。TSF19细胞贴壁生长,群体倍增时间为24.9小时。染色体分析表明,在第4代细胞传代之前,超过90%的细胞为二倍体。乳酸脱氢酶和苹果酸脱氢酶的同工酶分析表明,TSF19细胞未受到其他物种的交叉污染。细胞系细菌、真菌或支原体污染检测结果也为阴性。将编码荧光蛋白pEGFP-N3、pECFP-N1、pDsRed1-N1和pEYFP-N1的质粒转染到细胞中,以研究外源基因在细胞中的表达。质粒转染效率在21.8%至46.5%之间。这个新建立的细胞系不仅将在细胞水平上保存重要的特克塞尔绵羊的遗传资源,还将为基因组学、后基因组学、体细胞克隆研究提供有价值的资源。