Noninvasive optical imaging of apoptosis by caspase-targeted activity-based probes

被引:228
作者
Edgington, Laura E. [1 ]
Berger, Alicia B. [1 ]
Blum, Galia [2 ]
Albrow, Victoria E. [2 ]
Paulick, Margot G. [2 ]
Lineberry, Neil [3 ]
Bogyo, Matthew [1 ,2 ,4 ]
机构
[1] Stanford Univ, Sch Med, Canc Biol Program, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Pathol, Sch Med, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Immunol, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Microbiol & Immunol, Sch Med, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
FLUOROCHROME-LABELED INHIBITORS; DEATH IN-VIVO; CELL-DEATH; ANNEXIN-V; DNA FRAGMENTATION; TUMOR RESPONSE; ACTIVATION; CHEMOTHERAPY; PEPTIDE; VISUALIZATION;
D O I
10.1038/nm.1938
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Imaging agents that enable direct visualization and quantification of apoptosis in vivo have great potential value for monitoring chemotherapeutic response as well as for early diagnosis and disease monitoring. We describe here the development of fluorescently labeled activity-based probes (ABPs) that covalently label active caspases in vivo. We used these probes to monitor apoptosis in the thymi of mice treated with dexamethasone as well as in tumor-bearing mice treated with the apoptosis-inducing monoclonal antibody Apomab (Genentech). Caspase ABPs provided direct readouts of the kinetics of apoptosis in live mice, whole organs and tissue extracts. The probes produced a maximum fluorescent signal that could be monitored noninvasively and that coincided with the peak in caspase activity, as measured by gel analysis. Overall, these studies demonstrate that caspase-specific ABPs have the potential to be used for noninvasive imaging of apoptosis in both preclinical and clinical settings.
引用
收藏
页码:967 / U177
页数:8
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