A Near-Infrared Cell Tracker Reagent for Multiscopic In Vivo Imaging and Quantification of Leukocyte Immune Responses

被引:51
作者
Swirski, Filip K. [1 ,2 ]
Berger, Cedric R. [1 ,2 ]
Figueiredo, Jose-Luiz [1 ,2 ]
Mempel, Thorsten R. [3 ]
von Andrian, Ulrich H. [4 ,5 ]
Pittet, Mikael J. [1 ,2 ,6 ]
Weissleder, Ralph [1 ,2 ,6 ]
机构
[1] Massachusetts Gen Hosp, Ctr Mol Imaging Res, Charlestown, MA USA
[2] Harvard Univ, Sch Med, Charlestown, MA USA
[3] Massachusetts Gen Hosp, Ctr Immunol & Inflammatory Dis, Charlestown, MA USA
[4] Harvard Univ, Sch Med, CBR Inst Biomed Res, Boston, MA USA
[5] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[6] Massachusetts Gen Hosp, Ctr Syst Biol, Boston, MA USA
来源
PLOS ONE | 2007年 / 2卷 / 10期
关键词
D O I
10.1371/journal.pone.0001075
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The complexity of the tumor microenvironment necessitates that cell behavior is studied in a broad, multi-scale context. Although tomographic and microscopy-based far and near infrared fluorescence (NIRF, >650 nm) imaging methods offer high resolution, sensitivity, and depth penetration, there has been a lack of optimized NIRF agents to label and track cells in their native environments at different scales. In this study we labeled mammalian leukocytes with VivoTag 680 (VT680), an amine reactive N-hydroxysuccinimide (NHS) ester of a (benz) indolium-derived far red fluorescent probe. We show that VT680 diffuses into leukocytes within minutes, covalently binds to cellular components, remains internalized for days in vitro and in vivo, and does not transfer fluorescence to adjacent cells. It is biocompatible, keeps cells fully functional, and fluoresces at high intensities. In a tumor model of cytotoxic T lymphocyte (CTL) immunotherapy, we track and quantify VT680-labeled cells longitudinally at the whole-body level with fluorescence-mediated molecular tomography (FMT), within tissues at single cell resolutions by multiphoton and confocal intravital microscopy, and ex vivo by flow cytometry. Thus, this approach is suitable to monitor cells at multiple resolutions in real time in their native environments by NIR-based fluorescence imaging.
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页数:7
相关论文
共 18 条
[1]   Calcium oscillations regulate thymocyte motility during positive selection in the three-dimensional thymic environment [J].
Bhakta, NR ;
Oh, DY ;
Lewis, RS .
NATURE IMMUNOLOGY, 2005, 6 (02) :143-151
[2]   In vivo imaging of cytotoxic T cell infiltration and elimination of a solid tumor [J].
Boissonnas, Alexandre ;
Fetler, Luc ;
Zeelenberg, Ingrid S. ;
Hugues, Stphanie ;
Amigorena, Sebastian .
JOURNAL OF EXPERIMENTAL MEDICINE, 2007, 204 (02) :345-356
[3]   Dynamics of CD8+ T cell priming by dendritic cells in intact lymph nodes [J].
Bousso, P ;
Robey, E .
NATURE IMMUNOLOGY, 2003, 4 (06) :579-585
[4]   Dynamics of thymocyte-stromal cell interactions visualized by two-photon microscopy [J].
Bousso, P ;
Bhakta, NR ;
Lewis, RS ;
Robey, E .
SCIENCE, 2002, 296 (5574) :1876-1880
[5]   Regulatory T cells suppress tumor-specific CD8 T cell cytotoxicity through TGF-β signals in vivoi [J].
Chen, ML ;
Pittet, MJ ;
Gorelik, L ;
Flavell, RA ;
Weissleder, R ;
von Boehmer, H ;
Khazaie, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (02) :419-424
[6]   Eradication of established tumors by CD8+ T cell adoptive immunotherapy [J].
Hanson, HL ;
Donermeyer, DL ;
Ikeda, H ;
White, JM ;
Shankaran, V ;
Old, LJ ;
Shiku, H ;
Schreiber, RD ;
Allen, PM .
IMMUNITY, 2000, 13 (02) :265-276
[7]  
Huang AL, 2006, NATURE, V442, P934, DOI [10.1038/nature05084, 10.1038/nature050084]
[8]  
LEHR HA, 1993, LAB INVEST, V68, P388
[9]   DETERMINATION OF LYMPHOCYTE DIVISION BY FLOW-CYTOMETRY [J].
LYONS, AB ;
PARISH, CR .
JOURNAL OF IMMUNOLOGICAL METHODS, 1994, 171 (01) :131-137
[10]   Regulatory T cells reversibly suppress cytotoxic T cell function independent of effector differentiation [J].
Mempel, Thorsten R. ;
Pittet, Mikael J. ;
Khazaie, Khashayarsha ;
Weninger, Wolfgang ;
Weissleder, Ralph ;
von Boehmer, Harald ;
von Andrian, Ulrich H. .
IMMUNITY, 2006, 25 (01) :129-141