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Imaging of Apoptosis

University of Washington
Seattle, Washington

Correspondence: For correspondence or reprints contact: Jonathan Tait, Department of Laboratory Medicine, University of Washington, Box 357110, Seattle, WA 98195-7110. E-mail: tait{at}u.washington.edu

ABSTRACT

Cells can die by several pathways, such as accidental death, apoptosis, autophagy, pyroptosis, and oncosis. These are important in normal physiology and many disease states, such as cancer and cardiovascular disease. Specific biochemical changes occur in cells undergoing apoptosis that provide potential targets for molecular imaging agents. Several of these molecular steps have been evaluated to date, including phosphatidylserine exposure at the extracellular face of the plasma membrane, detected by proteins such as annexin V; caspase activation in the intracellular compartment, detected by labeled enzyme substrates or inhibitors; and mitochondrial membrane potential collapse, detected by reduced levels of phosphonium cations that normally accumulate in healthy mitochondria. Phase I clinical trials have been performed with 1 of these agents, annexin V. Future work will likely include development of new agents that detect targets not exploited by current agents, translational research on the significance of imaging the different forms of cell death, and further improvements in the techniques for labeling existing agents to improve sensitivity and reduce nonspecific background.

Key Words: molecular biology • molecular imaging • radiochemistry • apoptosis • imaging • annexins

FOOTNOTES

COPYRIGHT © 2008 by the Society of Nuclear Medicine, Inc.

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