Comprehensive assessment of quantum dots for multispectral twophoton imaging of dynamic leukocyte migration in lymph nodes

IntraVital Pub Date : 2013-04-01 DOI:10.4161/intv.25745
D. Natale, S. Soriano, F. Coelho, Miroslav Hons, J. Stein
{"title":"Comprehensive assessment of quantum dots for multispectral twophoton imaging of dynamic leukocyte migration in lymph nodes","authors":"D. Natale, S. Soriano, F. Coelho, Miroslav Hons, J. Stein","doi":"10.4161/intv.25745","DOIUrl":null,"url":null,"abstract":"In recent years, intravital twophoton microscopy (2PM) has emerged as the appropriate technique for direct in situ imaging of immune cell dynamics inside peripheral lymph nodes (PLNs) of live, anesthetized mice, yielding important insights into the regulation of immune responses. However, most current 2PM approaches are limited by the scarce availability of near-infrared (NIR) probes for multispectral time-lapse imaging, and by the use of a single excitation wavelength for multiple fluorophores. The recent availability of quantum dots (QDs) nanoparticles displaying unique optical properties have the potential to overcome this limitation but their suitability has not been yet comprehensively tested for 2PM imaging in vivo. In this study, we explored the use and delivery of NIR-emitting QDs into dendritic cells. Furthermore, we functionalized the surface of these nanoparticles with antibodies that recognize specific antigens expressed on the endothelium of the PLN microvasculature or their use as NIR plasma markers and examined the homeostatic recirculation of lymphocytes. This approach allowed to simultaneously visualize up to six different cell populations and lymphoid structures and identified varying lymphocyte migration patterns in defined microenvironments. Yet, QDs were more difficult to reproducibly couple to antibodies and showed a tendency to cause clustering of targeted antigens. Our data provide an in-depth analysis of the usefulness and shortcomings of QDs as imaging tools for anatomical landmarking in 2PM studies.","PeriodicalId":14512,"journal":{"name":"IntraVital","volume":"62 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2013-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IntraVital","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4161/intv.25745","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

In recent years, intravital twophoton microscopy (2PM) has emerged as the appropriate technique for direct in situ imaging of immune cell dynamics inside peripheral lymph nodes (PLNs) of live, anesthetized mice, yielding important insights into the regulation of immune responses. However, most current 2PM approaches are limited by the scarce availability of near-infrared (NIR) probes for multispectral time-lapse imaging, and by the use of a single excitation wavelength for multiple fluorophores. The recent availability of quantum dots (QDs) nanoparticles displaying unique optical properties have the potential to overcome this limitation but their suitability has not been yet comprehensively tested for 2PM imaging in vivo. In this study, we explored the use and delivery of NIR-emitting QDs into dendritic cells. Furthermore, we functionalized the surface of these nanoparticles with antibodies that recognize specific antigens expressed on the endothelium of the PLN microvasculature or their use as NIR plasma markers and examined the homeostatic recirculation of lymphocytes. This approach allowed to simultaneously visualize up to six different cell populations and lymphoid structures and identified varying lymphocyte migration patterns in defined microenvironments. Yet, QDs were more difficult to reproducibly couple to antibodies and showed a tendency to cause clustering of targeted antigens. Our data provide an in-depth analysis of the usefulness and shortcomings of QDs as imaging tools for anatomical landmarking in 2PM studies.
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
量子点对淋巴结中动态白细胞迁移的多光谱双光子成像的综合评价
近年来,活体双光子显微镜(2PM)已成为活体麻醉小鼠外周淋巴结(pln)内免疫细胞动力学直接原位成像的合适技术,对免疫反应的调节提供了重要的见解。然而,大多数目前的2PM方法受到近红外(NIR)探针用于多光谱延时成像的稀缺性以及使用单一激发波长用于多个荧光团的限制。最近可用的量子点(QDs)纳米颗粒具有独特的光学特性,有可能克服这一限制,但其适用性尚未全面测试用于体内2PM成像。在这项研究中,我们探索了nir发射量子点在树突状细胞中的使用和传递。此外,我们用抗体功能化这些纳米颗粒的表面,这些抗体可以识别在PLN微血管内皮上表达的特定抗原或将其用作近红外血浆标记物,并检测淋巴细胞的稳态再循环。这种方法允许同时可视化多达六种不同的细胞群和淋巴样结构,并确定在确定的微环境中不同的淋巴细胞迁移模式。然而,量子点更难与抗体重复偶联,并有引起目标抗原聚集的倾向。我们的数据深入分析了量子点作为2PM研究中解剖地标成像工具的有用性和缺点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Intravital characterization of tumor cell migration in pancreatic cancer. An intravital microscopy model to study early pancreatic inflammation in type 1 diabetes in NOD mice. Direct visualization of the phenotype of hypoxic tumor cells at single cell resolution in vivo using a new hypoxia probe Validation of a device for the active manipulation of the tumor microenvironment during intravital imaging Intravital multiphoton imaging of mouse tibialis anterior muscle.
×
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