Role of Bcl-2 Family Members in Anoxia Induced Cell Death

Emelyn H. Shroff, Colleen Snyder and Navdeep Chandel

volume 6 | issue 7

1 April 2007
Pages: 807 - 809

We now provide open access to journal articles published online for one year or more. This article may be downloaded at the following link:

Download PDF

If the document does not open, please right-click on the link (control-click on a Macintosh) and select the option to save the file to disk.

Anoxia, the condition of oxygen deprivation, induces apoptosis via the intrinsic apoptotic pathway. Cells deficient in both Bax and Bak do not undergo cell death during anoxia. However, the underlying mechanism of anoxia induced cell death is not well defined. Here we report our latest findings of two critical events that are required to induce cell death during anoxia. First, a key member of the Bcl-2 family of pro-survival proteins, Mcl-1, undergoes proteasomal-dependent degradation. The loss of Mcl-1 protein is independent of Bax or Bak indicating this is an early event in the apoptotic cascade. Second, cells inhibit the mitochondrial electron transport chain to negate the pro-survival function of Bcl- 2/Bcl-XL. These observations indicate that loss of pro-survival function is necessary for anoxia induced cell death.

Authors

Emelyn H. Shroff

Northwestern University Medical Center; Chicago IL, USA

Colleen Snyder

Northwestern University Medical Center; Chicago IL, USA

Navdeep Chandel

Northwestern University Medical School; Chicago, IL USA

We now provide open access to journal articles published online for one year or more. This article may be downloaded at the following link: