A novel, high conductance channel of mitochondria linked to apoptosis in mammalian cells and Bax expression in yeast

Author:

Pavlov Evgeny V.1,Priault Muriel2,Pietkiewicz Dawn1,Cheng Emily H.-Y.3,Antonsson Bruno4,Manon Stephen2,Korsmeyer Stanley J.3,Mannella Carmen A.5,Kinnally Kathleen W.1

Affiliation:

1. Division of Basic Sciences, New York University College of Dentistry, New York, NY 10010

2. Institut de Biochimie et Génétique Cellulaires/Centre National de la Recherche Scientifique, F-33077 Bordeaux, France

3. Departments of Pathology and Medicine, Harvard Medical School, Dana-Farber Cancer Institute, Howard Hughes Medical Institute, Boston, MA 02115

4. Serono Pharmaceutical Research Institute, Serono International S.A., CH-1228 Plan-les Ouates, Geneva, Switzerland

5. Wadsworth Center, New York State Department of Health, Albany, NY 12203

Abstract

During apoptosis, proapoptotic factors are released from mitochondria by as yet undefined mechanisms. Patch-clamping of mitochondria and proteoliposomes formed from mitochondrial outer membranes of mammalian (FL5.12) cells has uncovered a novel ion channel whose activity correlates with onset of apoptosis. The pore diameter inferred from the largest conductance state of this channel is ∼4 nm, sufficient to allow diffusion of cytochrome c and even larger proteins. The activity of the channel is affected by Bcl-2 family proteins in a manner consistent with their pro- or antiapoptotic properties. Thus, the channel activity correlates with presence of proapoptotic Bax in the mitochondrial outer membrane and is absent in mitochondria from cells overexpressing antiapoptotic Bcl-2. Also, a similar channel activity is found in mitochondrial outer membranes of yeast expressing human Bax. These findings implicate this channel, named mitochondrial apoptosis–induced channel, as a candidate for the outer-membrane pore through which cytochrome c and possibly other factors exit mitochondria during apoptosis.

Publisher

Rockefeller University Press

Subject

Cell Biology

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