一种实用的装置,可以精确地将分子传递到培养的多个神经元中。

Brain cell biology Pub Date : 2006-12-01 Epub Date: 2008-04-05 DOI:10.1007/s11068-008-9021-z
Chikako Hara, Kiyohiko Tateyama, Naoki Akamatsu, Hiroyuki Imabayashi, Koichi Karaki, Nobuo Nomura, Hideyuki Okano, Atsushi Miyawaki
{"title":"一种实用的装置,可以精确地将分子传递到培养的多个神经元中。","authors":"Chikako Hara,&nbsp;Kiyohiko Tateyama,&nbsp;Naoki Akamatsu,&nbsp;Hiroyuki Imabayashi,&nbsp;Koichi Karaki,&nbsp;Nobuo Nomura,&nbsp;Hideyuki Okano,&nbsp;Atsushi Miyawaki","doi":"10.1007/s11068-008-9021-z","DOIUrl":null,"url":null,"abstract":"<p><p>We have developed a device for pinpoint delivery of chemicals, proteins, and nucleic acids into cultured cells. The principle underlying the technique is the flow of molecules from the culture medium into cells through a rupture in the plasma membrane made by a needle puncture. DNA transfection is achieved by stabbing the needle tip into the nucleus. The CellBee device can be attached to any inverted microscope, and molecular delivery can be coupled with conventional live cell imaging. Because the position of the needle relative to the targeted cultured cells is computer-controlled, efficient delivery of molecules such as rhodamine into as many as 100 HeLa cells can be completed in 10 min. Moreover, specific target cells within a single dish can be transfected with multiple DNA constructs by simple changes of culture medium containing different plasmids. In addition, the nano-sized needle tip enables gentle molecular delivery, minimizing cell damage. This method permits DNA transfection into specific hippocampal neurons without disturbing neuronal circuitry established in culture.</p>","PeriodicalId":72445,"journal":{"name":"Brain cell biology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2006-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s11068-008-9021-z","citationCount":"16","resultStr":"{\"title\":\"A practical device for pinpoint delivery of molecules into multiple neurons in culture.\",\"authors\":\"Chikako Hara,&nbsp;Kiyohiko Tateyama,&nbsp;Naoki Akamatsu,&nbsp;Hiroyuki Imabayashi,&nbsp;Koichi Karaki,&nbsp;Nobuo Nomura,&nbsp;Hideyuki Okano,&nbsp;Atsushi Miyawaki\",\"doi\":\"10.1007/s11068-008-9021-z\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>We have developed a device for pinpoint delivery of chemicals, proteins, and nucleic acids into cultured cells. The principle underlying the technique is the flow of molecules from the culture medium into cells through a rupture in the plasma membrane made by a needle puncture. DNA transfection is achieved by stabbing the needle tip into the nucleus. The CellBee device can be attached to any inverted microscope, and molecular delivery can be coupled with conventional live cell imaging. Because the position of the needle relative to the targeted cultured cells is computer-controlled, efficient delivery of molecules such as rhodamine into as many as 100 HeLa cells can be completed in 10 min. Moreover, specific target cells within a single dish can be transfected with multiple DNA constructs by simple changes of culture medium containing different plasmids. In addition, the nano-sized needle tip enables gentle molecular delivery, minimizing cell damage. This method permits DNA transfection into specific hippocampal neurons without disturbing neuronal circuitry established in culture.</p>\",\"PeriodicalId\":72445,\"journal\":{\"name\":\"Brain cell biology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2006-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1007/s11068-008-9021-z\",\"citationCount\":\"16\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Brain cell biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1007/s11068-008-9021-z\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2008/4/5 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain cell biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1007/s11068-008-9021-z","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2008/4/5 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 16

摘要

我们已经开发出一种设备,可以精确地将化学物质、蛋白质和核酸输送到培养的细胞中。该技术的基本原理是,分子从培养基中流入细胞,通过针刺在质膜上造成的破裂。DNA转染是通过将针尖插入细胞核来实现的。CellBee装置可以附着在任何倒置显微镜上,分子传递可以与传统的活细胞成像相结合。由于针头相对于目标培养细胞的位置是由计算机控制的,因此可以在10分钟内将罗丹明等分子有效地递送到多达100个HeLa细胞中。此外,通过简单地改变含有不同质粒的培养基,可以将单个培养皿中的特定靶细胞转染多种DNA构建物。此外,纳米大小的针尖能够温和地传递分子,最大限度地减少细胞损伤。这种方法允许将DNA转染到特定的海马神经元中,而不干扰培养中建立的神经元回路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
A practical device for pinpoint delivery of molecules into multiple neurons in culture.

We have developed a device for pinpoint delivery of chemicals, proteins, and nucleic acids into cultured cells. The principle underlying the technique is the flow of molecules from the culture medium into cells through a rupture in the plasma membrane made by a needle puncture. DNA transfection is achieved by stabbing the needle tip into the nucleus. The CellBee device can be attached to any inverted microscope, and molecular delivery can be coupled with conventional live cell imaging. Because the position of the needle relative to the targeted cultured cells is computer-controlled, efficient delivery of molecules such as rhodamine into as many as 100 HeLa cells can be completed in 10 min. Moreover, specific target cells within a single dish can be transfected with multiple DNA constructs by simple changes of culture medium containing different plasmids. In addition, the nano-sized needle tip enables gentle molecular delivery, minimizing cell damage. This method permits DNA transfection into specific hippocampal neurons without disturbing neuronal circuitry established in culture.

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
期刊最新文献
Editorial: Hello, goodbye. Imaging activity of neuronal populations with new long-wavelength voltage-sensitive dyes. Differences in c-jun and nNOS expression levels in motoneurons following different kinds of axonal injury in adult rats. Direct interaction of SNARE complex binding protein synaphin/complexin with calcium sensor synaptotagmin 1 O-GlcNAc modification of radial glial vimentin filaments in the developing chick brain
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1