Abstract
Apoptosis, or programmed cell death, is an essential process for normal embryonic development, maintaining homeostasis in adult tissues, and suppressing carcinogenesis. The bcl-2 protein, discovered in association with follicular lymphoma, plays a prominent role in controlling apoptosis and enhancing cell survival in response to diverse apoptotic stimuli. The evolutionarily conserved bcl-2 protein is now recognized as being a member of a family of related proteins which can be categorized as death agonists or death antagonists. Progress in defining the role of bcl-2 and its family members in regulating apoptosis is rapidly advancing. This review describes, in detail, current bcl-2 family members and the possible mechanisms of function which allow the bcl-2 family of proteins to either promote or suppress cell death.
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Abbreviations
- BH:
-
bcl-2 homology domain
- DNA-PK:
-
DNA-dependent protein kinase
- ER:
-
endoplasmic reticulum
- ICE:
-
interleukin 1β converting enzyme
- Ig:
-
immunoglobulin
- KO:
-
knockout
- NPC:
-
nuclear pore complex
- PARP:
-
poly ADP-dependent polymerase
- PEST:
-
proline-glutamate-serine-threonine
- PKC:
-
protein kinase C
- PT:
-
permeability transition
- ROS:
-
reactive oxygen species
- SM:
-
sphingomyelin
- Smase:
-
sphingomyelinase
- snRNPs:
-
small nuclear ribonuclear proteins
- SV:
-
Sindbis virus
- TG:
-
thapsigargin
- TNF:
-
tumor necrosis factor α
- TPA:
-
phorbol 12-myristate 13-acetate
- UTR:
-
untranslated region
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Bruckheimer, E.M., Cho, S.H., Sarkiss, M., Herrmann, J., McDonnell, T.J. (1998). The Bcl-2 gene family and apoptosis. In: Al-Rubeai, M. (eds) Apoptosis. Advances in Biochemical Engineering/Biotechnology, vol 62. Springer, Berlin, Heidelberg. https://doi.org/10.1007/BFb0102306
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