Development and evaluation of a non-peptidic ligand for the molecular imaging of inflammatory processes using S100A9 (MRP14) as a novel target

被引:16
|
作者
Faust, A. [1 ,2 ]
Voeller, T. [3 ]
Busch, F. [1 ]
Schaefers, M. [1 ,2 ,4 ,5 ]
Roth, J. [2 ,3 ,5 ]
Hermann, S. [1 ,2 ,5 ]
Vogl, T. [2 ,5 ]
机构
[1] Univ Munster, EIMI, D-48149 Munster, Germany
[2] Univ Munster, Cells In Mot Cluster Excellence EXC 1003 CiM, D-48149 Munster, Germany
[3] Univ Hosp Munster, Inst Immunol, D-48149 Munster, Germany
[4] Univ Hosp Munster, Dept Nucl Med, D-48149 Munster, Germany
[5] Univ Munster, Interdisciplinary Ctr Clin Res IZKF Munster, D-48149 Munster, Germany
关键词
RECEPTOR; 4; MYELOID-RELATED-PROTEIN-8/14; PROTEINS;
D O I
10.1039/c5cc07019h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The establishment of novel molecular imaging tools to monitor the local activity of inflammation remains an interdisciplinary challenge. Our target, the alarmin S100A9, one subunit of the heterodimer S100A8/S100A9 (calprotectin), is locally secreted in high concentrations from immigrated and activated phagocytes at local sites of inflammation. Calprotectin is already a well established serum biomarker for many inflammatory disorders. Here we show the development and first evaluation of the novel S100A9 specific molecular imaging probe Cy5.5-CES271 for optical imaging of local inflammatory activity in vivo.
引用
收藏
页码:15637 / 15640
页数:4
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