page 875, Metkar et al. overturn this view, showing that in the dominant pathway granzyme B begins by processing procaspase-3, whereas mitochondria are secondary components that amplify the signal once caspase-3 has been activated. The work adds to recent evidence that caspases can initiate apoptosis, whereas mitochondria serve as signal amplifiers.
The authors used a variety of strategies to avoid common pitfalls during granzyme- mediated apoptosis assays. In past assays, uncomplexed granzyme B was added to cell extracts. Granzyme B in the new assays was delivered into cells using adenovirus particles, and was presented in a complex with the proteoglycan serglycin to mimic the enzyme's natural state. Doing the apoptosis assays with whole cells minimized the risk of proteolysis occurring at sites not normally frequented by granzyme B.
In this system, Bid cleavage was not detected, and cells deficient in procaspase-3 failed to undergo mitochondrial depolarization or DNA fragmentation, indicating that granzyme B acts first through procaspase-3 rather than the mitochondria. Caspase-3–induced permeabilization of the mitochondria amplifies the death signal but, based on assays with cells harboring a Bax/Bak deletion, this amplification is not essential for apoptosis. ▪