Journal article
Loss of Mcl-1 protein and inhibition of electron transport chain together induce anoxic cell death
JK Brunelle, EH Shroff, H Perlman, A Strasser, CT Moraes, RA Flavell, NN Danial, B Keith, CB Thompson, NS Chandel
Molecular and Cellular Biology | Published : 2007
DOI: 10.1128/MCB.01535-06
Abstract
How cells die in the absence of oxygen (anoxia) is not understood. Here we report that cells deficient in Bax and Bak or caspase-9 do not undergo anoxia-induced cell death. However, the caspase-9 null cells do not snrvive reoxygenation due to the generation of mitochondrial reactive oxygen species. The individual loss of Bim, Bid, Puma, Noxa, Bad, caspase-2, or hypoxia-inducible factor 1β, which are potential upstream regulators of Bax or Bak, did not prevent anoxia-induced cell death. Anoxia triggered the loss of the Mcl-1 protein upstream of Bax/Bak activation. Cells containing a mitochondrial DNA cytochrome b 4-base-pair deletion ([rho-] cells) and cells depleted of their entire mitochond..
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Awarded by National Heart, Lung, and Blood Institute