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Clonal chromosomal and genomic instability during human multipotent mesenchymal stromal cells long-term culture.人多能间充质基质细胞长期培养过程中的克隆性染色体和基因组不稳定性。
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The ghosts of HeLa: How cell line misidentification contaminates the scientific literature.海拉细胞的幽灵:细胞系错误鉴定如何污染科学文献。
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3
Identification and characterization of heptapeptide modulators of the glycine receptor.甘氨酸受体七肽调节剂的鉴定与表征
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Cytotoxic and antioxidant properties of active principals isolated from water hyacinth against four cancer cells lines.水葫芦中活性成分对四种癌细胞系的细胞毒性和抗氧化特性。
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Guidelines for the use of cell lines in biomedical research.生物医学研究中细胞系使用指南。
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Clinical biospecimens: reference materials, certified for nominal properties?临床生物样本:针对标称特性进行认证的参考物质?
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Identification of novel specific allosteric modulators of the glycine receptor using phage display.利用噬菌体展示技术鉴定甘氨酸受体的新型别构调节剂。
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Identification of cross-contaminated animal cells by PCR and isoenzyme analysis.通过 PCR 和同工酶分析鉴定交叉污染的动物细胞。
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本文引用的文献

1
The serial cultivation of human diploid cell strains.人二倍体细胞株的连续培养。
Exp Cell Res. 1961 Dec;25:585-621. doi: 10.1016/0014-4827(61)90192-6.
2
Differential regulation of liver-specific and ubiquitously-expressed genes in primary rat hepatocytes by the extracellular matrix.细胞外基质对原代大鼠肝细胞中肝脏特异性基因和普遍表达基因的差异调节
Cell Physiol Biochem. 2001;11(1):33-40. doi: 10.1159/000047790.
3
Cell contamination leads to inaccurate data: we must take action now.细胞污染会导致数据不准确:我们现在必须采取行动。
Nature. 2000 Jan 27;403(6768):356. doi: 10.1038/35000394.
4
Widespread intraspecies cross-contamination of human tumor cell lines arising at source.源自源头的人类肿瘤细胞系广泛存在种内交叉污染。
Int J Cancer. 1999 Nov 12;83(4):555-63. doi: 10.1002/(sici)1097-0215(19991112)83:4<555::aid-ijc19>3.0.co;2-2.
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Induction of tyrosine aminotransferase of primary cultured rat hepatocytes depends on the organization of microtubules.
J Cell Physiol. 1998 Apr;175(1):41-9. doi: 10.1002/(SICI)1097-4652(199804)175:1<41::AID-JCP5>3.0.CO;2-C.
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Establishment and characterization of a nontumorigenic cell line derived from a human hepatocellular adenoma expressing hepatocyte-specific markers.
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7
Evidence for multiple pathways to cellular senescence.
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8
HLA-A, B, C and DR alloantigen expression on forty-six cultured human tumor cell lines.46种培养的人肿瘤细胞系上HLA - A、B、C和DR同种异体抗原的表达
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9
Cross-contamination of cells in culture.培养细胞中的交叉污染。
Science. 1981 Apr 24;212(4493):446-52. doi: 10.1126/science.6451928.
10
Complexity of expression of antigenic determinants, recognized by monoclonal antibodies HMFG-1 and HMFG-2, in normal and malignant human mammary epithelial cells.单克隆抗体HMFG-1和HMFG-2识别的抗原决定簇在正常和恶性人乳腺上皮细胞中的表达复杂性。
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细胞系来源。

Cell line provenance.

机构信息

Cancer Research UK Department of Medical Oncology, Glasgow University, Garscube Estate, Bearsden, Glasgow, U.K. (E-mail,

出版信息

Cytotechnology. 2002 Jul;39(2):55-67. doi: 10.1023/A:1022949730029.

DOI:10.1023/A:1022949730029
PMID:19003293
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3463983/
Abstract

Cultured cell lines have become an extremely valuable resource, both in academic research and in industrial biotechnology. However, their value is frequently compromised by misidentification and undetected microbial contamination. As detailed elsewhere in this volume, the technology, both simple and sophisticated, is available to remedy the problems of misidentification and contamination, given the will to apply it. Combined with proper records of the origin and history of the cell line, assays for authentication and contamination contribute to the provenance of the cell line. Detailed records should start from the initiation or receipt of the cell line, and should incorporate data on the donor as well as the tissue from which the cell line was derived, should continue with details of maintenance, and include any accidental as well as deliberate deviations from normal maintenance. Records should also contain details of authentication and regular checks for contamination. With this information, preferably stored in a database, and suitable backed up, the provenance of the cell line so created makes the cell line a much more valuable resource, fit for validation in industrial applications and more likely to provide reproducible experimental results when disseminated for research in other laboratories.

摘要

细胞培养系已成为学术研究和工业生物技术中极其宝贵的资源。然而,它们的价值经常因错误鉴定和未检测到的微生物污染而受到损害。正如本卷其他地方详细介绍的那样,如果有应用该技术的意愿,那么纠正错误鉴定和污染问题的技术,无论是简单的还是复杂的,都可用。结合细胞系来源和历史的适当记录,鉴定和污染检测有助于证明细胞系的出处。详细的记录应从细胞系的建立或接收开始,并应包含供体以及细胞系来源组织的相关数据,应继续记录细胞系的维护细节,包括任何意外和故意偏离正常维护的情况。记录还应包含鉴定和定期污染检测的详细信息。有了这些信息,最好存储在数据库中,并进行适当备份,这样创建的细胞系的出处就使细胞系成为更有价值的资源,适合在工业应用中进行验证,并且在分发到其他实验室进行研究时更有可能提供可重复的实验结果。