BAX and BAK1 are dispensable for ABT-737-induced dissociation of the BCL2-BECN1 complex and autophagy
Autophagy, 2015•Taylor & Francis
Disruption of the complex of BECN1 with BCL2 or BCL2L1/BCL-XL is an essential switch
that turns on cellular autophagy in response to environmental stress or treatment with BH3
peptidomimetics. Recently, it has been proposed that BCL2 and BCL2L1/BCL-XL may
inhibit autophagy indirectly through a mechanism dependent on the proapoptotic BCL2
family members, BAX and BAK1. Here we report that the BH3 mimetic, ABT-737, induces
autophagy in parallel with disruption of BCL2-BECN1 binding in 2 different apoptosis …
that turns on cellular autophagy in response to environmental stress or treatment with BH3
peptidomimetics. Recently, it has been proposed that BCL2 and BCL2L1/BCL-XL may
inhibit autophagy indirectly through a mechanism dependent on the proapoptotic BCL2
family members, BAX and BAK1. Here we report that the BH3 mimetic, ABT-737, induces
autophagy in parallel with disruption of BCL2-BECN1 binding in 2 different apoptosis …
Disruption of the complex of BECN1 with BCL2 or BCL2L1/BCL-XL is an essential switch that turns on cellular autophagy in response to environmental stress or treatment with BH3 peptidomimetics. Recently, it has been proposed that BCL2 and BCL2L1/BCL-XL may inhibit autophagy indirectly through a mechanism dependent on the proapoptotic BCL2 family members, BAX and BAK1. Here we report that the BH3 mimetic, ABT-737, induces autophagy in parallel with disruption of BCL2-BECN1 binding in 2 different apoptosis-deficient cell types lacking BAX and BAK1, namely in mouse embryonic fibroblasts cells and in human colon cancer HCT116 cells. We conclude that the BH3 mimetic ABT-737 induces autophagy through a BAX and BAK1-independent mechanism that likely involves disruption of BECN1 binding to antiapoptotic BCL2 family members.
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