Evaluation of [(18)F]-CP18 as a PET imaging tracer for apoptosis

Mol Imaging Biol. 2013 Dec;15(6):739-47. doi: 10.1007/s11307-013-0644-9.

Abstract

Purpose: We identified and validated [(18)F]-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 [(18)F]-CP18 were assessed in vivo. [(18)F]-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, [(18)F]-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 [(18)F]-CP18 retention in the dexamethasone-induced thymus of treated versus control mice.

Conclusions: We report the use [(18)F]-CP18 as a PET tracer for imaging apoptosis. Our data support further development of this tracer for clinical PET applications.

MeSH terms

  • Analysis of Variance
  • Animals
  • Apoptosis*
  • Caspase 3 / metabolism
  • Cell Line, Tumor
  • Dexamethasone / adverse effects
  • Glycopeptides / chemistry
  • Glycopeptides / pharmacokinetics*
  • Humans
  • Linear Models
  • Mice
  • Molecular Imaging / methods*
  • Positron-Emission Tomography / methods*
  • Radiopharmaceuticals / chemistry
  • Radiopharmaceuticals / pharmacokinetics
  • Thymus Gland / chemistry
  • Thymus Gland / drug effects
  • Tissue Distribution

Substances

  • CP-18 compound
  • Glycopeptides
  • Radiopharmaceuticals
  • Dexamethasone
  • Caspase 3