Homeostatic functions of BCL-2 proteins beyond apoptosis

Adv Exp Med Biol. 2010;687:1-32. doi: 10.1007/978-1-4419-6706-0_1.


Since its introduction in 1930 by physiologist Walter Bradford Cannon, the concept of homeostasis remains the cardinal tenet of biologic regulation. Cells have evolved a highly integrated network of control mechanisms, including positive and negative feedback loops, to safeguard homeostasis in face of a wide range of stimuli. Such control mechanisms ultimately orchestrate cell death, division and repair in a manner concordant with cellular energy and ionic balance to achieve proper biologic fitness. The interdependence of these homeostatic pathways is also evidenced by shared control points that decode intra- and extracellular cues into defined effector responses. As critical control points of the intrinsic apoptotic pathway, the BCL-2 family of cell death regulators plays an important role in cellular homeostasis. The different anti- and pro-apoptotic members of this family form a highly selective network of functional interactions that ultimately governs the permeabilization of the mitochondrial outer membrane and subsequent release of apoptogenic factors such as cytochrome c. The advent of loss- and gain-of-function genetic models for the various BCL-2 family proteins has not only provided important insights into apoptosis mechanisms but also uncovered unanticipated roles for these proteins in other physiologic pathways beyond apoptosis (Fig. 1). Here, we turn our attention to these alternative cellular functions for BCL-2 proteins. We begin with a brief introduction of the cast of characters originally known for their capacity to regulate apoptosis and continue to highlight recent advances that have shaped and reshaped our views on their physiologic relevance in integration of apoptosis with other homeostatic pathways.

Publication types

  • Review

MeSH terms

  • Animals
  • Apoptosis / physiology*
  • Autophagy / physiology
  • Calcium / metabolism
  • Cell Cycle / physiology
  • Cell Differentiation
  • DNA Damage
  • DNA Replication
  • Energy Metabolism
  • Glucose / metabolism
  • Homeostasis / physiology*
  • Mitochondria / metabolism
  • Mitochondria / ultrastructure
  • Proto-Oncogene Proteins c-bcl-2 / genetics
  • Proto-Oncogene Proteins c-bcl-2 / metabolism*
  • Signal Transduction / physiology
  • Voltage-Dependent Anion Channels / metabolism


  • Proto-Oncogene Proteins c-bcl-2
  • Voltage-Dependent Anion Channels
  • Glucose
  • Calcium