TY - JOUR
T1 - Evaluation of [18F]-CP18 as a PET imaging tracer for apoptosis
AU - Su, Helen
AU - Chen, Gang
AU - Gangadharmath, Umesh
AU - Gomez, Luis F.
AU - Liang, Qianwa
AU - Mu, Fanrong
AU - Mocharla, Vani P.
AU - Szardenings, A. Katrin
AU - Walsh, Joseph C.
AU - Xia, Chun Fang
AU - Yu, Chul
AU - Kolb, Hartmuth C.
N1 - The online version of this article (doi: 10.1007/s11307-013-0644-9 ) contains supplementary material, which is available to authorized users. This is a preview of subscription content, log in to check access.
PY - 2013/12
Y1 - 2013/12
N2 - Purpose: We identified and validated [18F]-CP18, a DEVD (the caspase 3 substrate recognition motif) containing substrate-based compound as an imaging tracer for caspase-3 activity in apoptotic cells. Procedures: CP18 was radiolabeled with fluorine-18 using click chemistry. The affinity and selectivity of CP18 for caspase-3 were evaluated in vitro. The biodistribution and metabolism pattern of [18F]-CP18 were assessed in vivo. [ 18F]-CP18 positron emission tomography (PET) scans were performed in a dexamethasone-induced thymic apoptosis mouse model. After imaging, the mice were sacrificed, and individual organs were collected, measured in a gamma counter, and tested for caspase-3 activity. Results: In vitro enzymatic caspase-3 assay demonstrated specific cleavage of CP18. In vivo, [ 18F]-CP18 is predominantly cleared through the kidneys and urine, and is rapidly eliminated from the bloodstream. There was a sixfold increase in caspase activity and a fourfold increase of [18F]-CP18 retention in the dexamethasone-induced thymus of treated versus control mice. Conclusions: We report the use [18F]-CP18 as a PET tracer for imaging apoptosis. Our data support further development of this tracer for clinical PET applications.
AB - Purpose: We identified and validated [18F]-CP18, a DEVD (the caspase 3 substrate recognition motif) containing substrate-based compound as an imaging tracer for caspase-3 activity in apoptotic cells. Procedures: CP18 was radiolabeled with fluorine-18 using click chemistry. The affinity and selectivity of CP18 for caspase-3 were evaluated in vitro. The biodistribution and metabolism pattern of [18F]-CP18 were assessed in vivo. [ 18F]-CP18 positron emission tomography (PET) scans were performed in a dexamethasone-induced thymic apoptosis mouse model. After imaging, the mice were sacrificed, and individual organs were collected, measured in a gamma counter, and tested for caspase-3 activity. Results: In vitro enzymatic caspase-3 assay demonstrated specific cleavage of CP18. In vivo, [ 18F]-CP18 is predominantly cleared through the kidneys and urine, and is rapidly eliminated from the bloodstream. There was a sixfold increase in caspase activity and a fourfold increase of [18F]-CP18 retention in the dexamethasone-induced thymus of treated versus control mice. Conclusions: We report the use [18F]-CP18 as a PET tracer for imaging apoptosis. Our data support further development of this tracer for clinical PET applications.
KW - Apoptosis
KW - Caspase
KW - Molecular imaging
KW - PET
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U2 - 10.1007/s11307-013-0644-9
DO - 10.1007/s11307-013-0644-9
M3 - Article
C2 - 23681757
SN - 1536-1632
VL - 15
SP - 739
EP - 747
JO - Molecular Imaging and Biology
JF - Molecular Imaging and Biology
IS - 6
ER -