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鲁西黄牛成纤维细胞库的建立及生物学特性

Establishment and biological characteristics of Luxi cattle fibroblast bank.

作者信息

Liu Changqing, Guo Yu, Guan Weijun, Ma Yuehui, Zhang Hong-Hai, Tang Xuexi

机构信息

Division of Life Sciences and Technology, Ocean University of China, Qingdao 266003, China.

出版信息

Tissue Cell. 2008 Dec;40(6):417-24. doi: 10.1016/j.tice.2008.04.005. Epub 2008 Jun 25.

Abstract

A fibroblast line from ear marginal tissue of Luxi cattle (LXCEM2/2) was successfully established by direct culturing of explants. Biological analysis showed that the population doubling time (PDT) for reviving cells was approximately 24h. Measurement of lactic dehydrogenase (LDH) and malic dehydrogenase (MDH) isoenzymes showed no cross-contamination among the cells. Karyotyping showed that the frequency of cells with chromosome number 2n=60 was 90.7-92.2%. Tests for bacteria, fungi, viruses and mycoplasma were negative. The efficiencies of expression of pEGFP-N3, pEYFP-N1 and pDsRed1-N1 were between 6.3% and 31.6% at 24h, 48h and 72h after transfer; at 24h, fluorescence was well distributed in the cytoplasm and nucleus except for some cryptomeric vesicles. Every index of the Luxi cattle cell line meets the quality control standards of the American Type Culture Collection (ATCC). Not only has the germline of this important cattle breed been preserved at the cell level, but also valuable material had been provided for genome, postgenome and somacloning research. Moreover, the establishment of this technical platform may provide both technical and theoretical support for storing the genetic resources of other animals and poultry at the cell level.

摘要

通过外植体直接培养,成功建立了来自鲁西黄牛耳缘组织的成纤维细胞系(LXCEM2/2)。生物学分析表明,复苏细胞的群体倍增时间(PDT)约为24小时。乳酸脱氢酶(LDH)和苹果酸脱氢酶(MDH)同工酶检测显示细胞间无交叉污染。核型分析表明,染色体数目为2n = 60的细胞频率为90.7 - 92.2%。细菌、真菌、病毒和支原体检测均为阴性。转染后24小时、48小时和72小时,pEGFP-N3、pEYFP-N1和pDsRed1-N1的表达效率在6.3%至31.6%之间;在24小时时,除了一些隐窝样小泡外,荧光在细胞质和细胞核中分布良好。鲁西黄牛细胞系的各项指标均符合美国典型培养物保藏中心(ATCC)的质量控制标准。该重要牛品种的种系不仅在细胞水平上得以保存,还为基因组、后基因组和体细胞克隆研究提供了宝贵材料。此外,该技术平台的建立可为在细胞水平上保存其他畜禽遗传资源提供技术和理论支持。

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