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Mechanisms of Bcl-2 in Programmed Cell Death

Mechanisms of Bcl-2 in Programmed Cell Death. Laura Beth Hill St. Edward’s University. Apoptosis. Essential for normal embryonic development Natural and pathological Morphologic characteristics Regulated by proteins in Bcl-2 family. The Apoptotic Process. Cell receives death signal

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Mechanisms of Bcl-2 in Programmed Cell Death

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  1. Mechanisms of Bcl-2 in Programmed Cell Death Laura Beth Hill St. Edward’s University

  2. Apoptosis • Essential for normal embryonic development • Natural and pathological • Morphologic characteristics • Regulated by proteins in Bcl-2 family

  3. The Apoptotic Process • Cell receives death signal • Mitochondrial membrane potential decreases • Transport of cytochrome c through membrane into cytosol • Cytochrome c binds to Apaf-1 • Caspase activity initiated • Cell degradation

  4. What is Bcl-2? • Family of proteins that includes promoters and inhibitors • Proto-oncogene • Localized to outer mitochondrial membrane

  5. Characteristics • Bcl-2 family members can homo- and heterodimerize • Participate in selective pore formation • Expressed at different rates during development

  6. FOCUS OF SEMINARPossible Mechanisms • Bcl-2 blocks release of cytochrome c from mitochondrial membrane (Yang, et al., 1997) • Bcl-2 forms channels in lipid membranes (Schendel, et al., 1997)

  7. Cytochrome c Model • Necessary for the initiation of apoptosis • Found in the mitochondrial intermembrane space • Localization suggests connection between Bcl-2 and cytochrome c

  8. HL-60cells neo cells bcl-2 cells Isolation Isolation Staurosporine Staurosporine Immunoblot analysis Immunoblot analysis

  9. Yang’s Results • Cytochrome c in neo cells showed cytosol increase, with corresponding decrease in mitochondria • No significant change of cytochrome c in mitochondria or cytosol of Bcl-2 cells

  10. Yang’s Conclusion • Bcl-2 prevents the release of cytochrome c • Mechanism by which Bcl-2 blocks release unknown • Structural similarity to bacterial toxins suggests pore-forming ability

  11. Channel Formation Model • Bcl-2 can regulate Ca2+ fluxes and protein transport • 3D structure of Bcl-xL is similar to the pore-forming domains of DT and the bacterial colicins

  12. Cells expressing Bcl-2 Wild-type Mutant Purification Purification Detection of single channels Detection of single channels

  13. Schendel’s Results • Bcl-2 formed ion-conducting pores in a manner similar to that of bacterial toxins • Bcl-2 mutant produced only non-specific Cl- efflux • Bcl-2 in planar lipid bilayers formed discrete cation-selective channels • Bcl-2 mutant did not form channels here

  14. Schendel’s Conclusions • Biophysical evidence proves that Bcl-2 forms channels in membranes • Channels reside in closed state • What controls opening and closing? • What does Bcl-2 transport? • How do pro-apoptotic proteins oppose anti-apoptotic proteins?

  15. Practical Importance • Adjustment of apoptotic threshold • Gene therapy to control neuronal death • Protection of developing nervous system against neurotoxins (e.g. EtOH)

  16. Acknowledgements St. Edward’s School of Natural Sciences faculty and staff

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