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Mcl-1 and Bcl-xL sequestration of Bak confers differential resistance to BH3-only proteins.

Colin HockingsAmber E AlsopStephanie C FennellErinna F LeeW Douglas FairlieGrant DewsonRuth M Kluck
Published in: Cell death and differentiation (2018)
The prosurvival Bcl-2 family proteins Mcl-1 and Bcl-xL inhibit apoptosis by sequestering BH3-only proteins such as Bid and Bim (MODE 1) or the effector proteins Bak and Bax (MODE 2). To better understand the contributions of MODE 1 and MODE 2 in blocking cell death, and thus how to bypass resistance to cell death, we examined prescribed mixtures of Bcl-2 family proteins. In a Bim and Bak mixture, Bcl-xL and Mcl-1 each sequestered not only Bim but also Bak as it became activated by Bim. In contrast, in a Bid and Bak mixture, Bcl-xL preferentially sequestered Bid while Mcl-1 preferentially sequestered Bak. Notably, Bcl-xL could sequester Bak in response to the BH3 mimetic ABT-737, despite this molecule targeting Bcl-xL. These findings highlight the importance of Bak sequestration in resistance to anti-cancer treatments, including BH3 mimetics.
Keyphrases
  • cell death
  • oxidative stress
  • magnetic resonance
  • magnetic resonance imaging
  • drug delivery
  • dendritic cells
  • endoplasmic reticulum stress
  • type iii