Abstract

BCL-2 homology 3 (BH3)-only proteins of the BCL-2 family such as tBID and BIM(EL) assist BAX-type proteins to breach the permeability barrier of the outer mitochondrial membrane, thereby allowing cytoplasmic release of cytochrome c and other active inducers of cell death normally confined to the mitochondrial inter-membrane space. However, the exact mechanism by which tBID and BIM(EL) aid BAX and its close homologues in this mitochondrial protein release remains enigmatic. Here, using pure lipid vesicles, we provide evidence that tBID acts in concert with BAX to 1) form large membrane openings through both BH3-dependent and BH3-independent mechanisms, 2) cause lipid transbilayer movement concomitant with membrane permeabilization, and 3) disrupt the lipid bilayer structure of the membrane by promoting positive monolayer curvature stress. None of these effects were observed with BAX when BIM(EL) was substituted for tBID. Based on these data, we propose a novel model in which tBID assists BAX not only via protein-protein but also via protein-lipid interactions to form lipidic pore-type non-bilayer structures in the outer mitochondrial membrane through which intermembrane prodeath molecules exit mitochondria during apoptosis.

Highlights

  • Mitochondria usually play a crucial role in the cellular commitment to apoptosis through the release of a variety of prodeath molecules from the intermembrane space into the cytosol [1]

  • TBID, but Not BIMEL, Works in Conjunction with BAX to Form Large Membrane Openings in large unilamellar vesicles (LUVs)—To elucidate the mechanism(s) by which BID and BIM assist BAX in the release of mitochondrial intermembrane apoptogenic factors, we first used an in vitro reconstitution system consisting of mitochondria freshly isolated from rat liver [43] and various combinations of recombinant purified proapoptotic proteins

  • We found that the combination of BAX and tBID is more potent in the release of vesicular fluorescein isothiocyanate-labeled dextrans (FDs)-70 than the BAX ϩ cleaved BID (cBID) combination (Fig. 1B)

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Summary

Introduction

Mitochondria usually play a crucial role in the cellular commitment to apoptosis through the release of a variety of prodeath molecules from the intermembrane space into the cytosol [1]. Our results support the notion that tBID acts in concert with BAX to form lipidic pores in the membrane of LUVs allowing for the release of macromolecules of the size of cytochrome c and other larger mitochondrial apoptogenic factors.

Results
Conclusion
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