Bcl-2-regulated apoptosis: mechanism and therapeutic potential

JM Adams, S Cory - Current opinion in immunology, 2007 - Elsevier
JM Adams, S Cory
Current opinion in immunology, 2007Elsevier
Apoptosis is essential for tissue homeostasis, particularly in the hematopoietic compartment,
where its impairment can elicit neoplastic or autoimmune diseases. Whether stressed cells
live or die is largely determined by interplay between opposing members of the Bcl-2 protein
family. Bcl-2 and its closest homologs promote cell survival, but two other factions promote
apoptosis. The BH3-only proteins sense and relay stress signals, but commitment to
apoptosis requires Bax or Bak. The BH3-only proteins appear to activate Bax and Bak …
Apoptosis is essential for tissue homeostasis, particularly in the hematopoietic compartment, where its impairment can elicit neoplastic or autoimmune diseases. Whether stressed cells live or die is largely determined by interplay between opposing members of the Bcl-2 protein family. Bcl-2 and its closest homologs promote cell survival, but two other factions promote apoptosis. The BH3-only proteins sense and relay stress signals, but commitment to apoptosis requires Bax or Bak. The BH3-only proteins appear to activate Bax and Bak indirectly, by engaging and neutralizing their pro-survival relatives, which otherwise constrain Bax and Bak from permeabilizing mitochondria. The Bcl-2 family may also regulate autophagy and mitochondrial fission/fusion. Its pro-survival members are attractive therapeutic targets in cancer and perhaps autoimmunity and viral infections.
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