Activation-dependent phases of T cells distinguished by use of optical tweezers and near infrared Raman spectroscopy

被引:48
作者
Mannie, MD [1 ]
McConnell, TJ
Xie, CG
Li, YQ
机构
[1] E Carolina Univ, Sch Med, Dept Microbiol & Immunol, Greenville, NC 27834 USA
[2] E Carolina Univ, Dept Biol, Greenville, NC 27858 USA
[3] E Carolina Univ, Dept Phys, Greenville, NC 27858 USA
关键词
Raman spectroscopy; optical tweezers; T cell activation; blastogenesis;
D O I
10.1016/j.jim.2004.11.020
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Near-infrared Raman spectroscopy may provide a highly sensitive, noninvasive means to identify activation status of leukocytes. The purpose of the current study was to establish Raman spectroscopic characteristics of T cell activation. Activation of the RsL.11 T cell clone in vitro with Con A resulted in specific decrements in band intensities at 785, 1048, 1093, and 1376 cm(-1) but did not alter a majority of other band intensities including those at 1004 cm(-1) (phenylalanine) and 1660 cm(-1) (amide bonds). Activation-dependent decrements in these band intensities occurred subsequent to IL-2 production and correlated closely with T cell blastogenesis. Activation-dependent decrements in these band intensities were not strictly a function of cell size because the same observations were noted in size-controlled comparisons of resting and activated T cells. Like the RsL.11 clone, freshly isolated thymocytes that were activated by Con A or IL-2 showed decrements in particular emissions. These findings indicate that near-infrared Raman spectroscopy can be used as a noninvasive technique to reveal the activation status of single living T cells. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:53 / 60
页数:8
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