无创,无标记,单层培养活细胞的定量表征

Jing Zhang, D. Morris, V. Sottile, J. Crowe, M. Somekh, M. Mather
{"title":"无创,无标记,单层培养活细胞的定量表征","authors":"Jing Zhang, D. Morris, V. Sottile, J. Crowe, M. Somekh, M. Mather","doi":"10.1109/FOI.2011.6154837","DOIUrl":null,"url":null,"abstract":"Cell culture is essential to many areas of biology ranging from the fundamental study of cell biology to the application of cells for therapeutic purposes in Regenerative Medicine. Common to all these areas is the need to characterise cell populations under culture. Currently, cell populations are routinely monitored using conventional biological analysis e.g. cell surface markers, gene expression. This approach is destructive, not suitable for in-process measurements and renders time course experiments impossible. Alternatively non-destructive approaches that assess cell morphology can also be used, with light microscopy techniques (e.g. bright field, phase contrast imaging) being the primary methods. These microscopy techniques can sometimes be combined with the use of exogenous labels such as fluorescent markers. This can provide functional information but has the disadvantage that such cell modifications are invasive and potentially toxic to the cells.","PeriodicalId":240419,"journal":{"name":"2011 Functional Optical Imaging","volume":"78 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2011-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Non-invasive, label free, quantitative characterisation of live cells in monolayer culture\",\"authors\":\"Jing Zhang, D. Morris, V. Sottile, J. Crowe, M. Somekh, M. Mather\",\"doi\":\"10.1109/FOI.2011.6154837\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Cell culture is essential to many areas of biology ranging from the fundamental study of cell biology to the application of cells for therapeutic purposes in Regenerative Medicine. Common to all these areas is the need to characterise cell populations under culture. Currently, cell populations are routinely monitored using conventional biological analysis e.g. cell surface markers, gene expression. This approach is destructive, not suitable for in-process measurements and renders time course experiments impossible. Alternatively non-destructive approaches that assess cell morphology can also be used, with light microscopy techniques (e.g. bright field, phase contrast imaging) being the primary methods. These microscopy techniques can sometimes be combined with the use of exogenous labels such as fluorescent markers. This can provide functional information but has the disadvantage that such cell modifications are invasive and potentially toxic to the cells.\",\"PeriodicalId\":240419,\"journal\":{\"name\":\"2011 Functional Optical Imaging\",\"volume\":\"78 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2011-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2011 Functional Optical Imaging\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/FOI.2011.6154837\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2011 Functional Optical Imaging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/FOI.2011.6154837","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

细胞培养对生物学的许多领域都是必不可少的,从细胞生物学的基础研究到细胞在再生医学中的治疗应用。所有这些领域的共同点是需要描述培养下的细胞群。目前,细胞群的常规监测使用传统的生物分析,如细胞表面标记,基因表达。这种方法是破坏性的,不适合在过程中测量,使时间过程实验不可能。另外,也可以使用评估细胞形态的非破坏性方法,光学显微镜技术(例如,明场,相对比成像)是主要方法。这些显微镜技术有时可以结合使用外源标记,如荧光标记。这可以提供功能信息,但缺点是这种细胞修饰是侵入性的,对细胞有潜在的毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Non-invasive, label free, quantitative characterisation of live cells in monolayer culture
Cell culture is essential to many areas of biology ranging from the fundamental study of cell biology to the application of cells for therapeutic purposes in Regenerative Medicine. Common to all these areas is the need to characterise cell populations under culture. Currently, cell populations are routinely monitored using conventional biological analysis e.g. cell surface markers, gene expression. This approach is destructive, not suitable for in-process measurements and renders time course experiments impossible. Alternatively non-destructive approaches that assess cell morphology can also be used, with light microscopy techniques (e.g. bright field, phase contrast imaging) being the primary methods. These microscopy techniques can sometimes be combined with the use of exogenous labels such as fluorescent markers. This can provide functional information but has the disadvantage that such cell modifications are invasive and potentially toxic to the cells.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信