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Gary M Fiskum

Gary M Fiskum

School of Medicine

Anesthesiology

School of Medicine

Program in Neuroscience

School of Medicine

Biochemistry and Molecular Biology

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The publication detail shows the title, authors (with indicators showing other profiled authors), information on the publishing organization, abstract and a link to the article in PubMed. This abstract is what is used to create the fingerprint of the publication. If any grants are referenced by the publication, they will be listed here as well.



Inhibition of mitochondrial neural cell death pathways by protein transduction of Bcl-2 family proteins.

Lucian Soane; Gary Fiskum (Profiled Author: Gary M Fiskum)

Department of Anesthesiology, School of Medicine, University of Maryland, 685 W. Baltimore Street, Baltimore, MD 21201, USA.
Journal of bioenergetics and biomembranes 2005;37(3):179-90.

Abstract

Bcl-2 and other closely related members of the Bcl-2 family of proteins inhibit the death of neurons and many other cells in response to a wide variety of pathogenic stimuli. Bcl-2 inhibition of apoptosis is mediated by its binding to pro-apoptotic proteins, e.g., Bax and tBid, inhibition of their oligomerization, and thus inhibition of mitochondrial outer membrane pore formation, through which other pro-apoptotic proteins, e.g., cytochrome c, are released to the cytosol. Bcl-2 also exhibits an indirect antioxidant activity caused by a sub-toxic elevation of mitochondrial production of reactive oxygen species and a compensatory increase in expression of antioxidant gene products. While classic approaches to cytoprotection based on Bcl-2 family gene delivery have significant limitations, cellular protein transduction represents a new and exciting approach utilizing peptides and proteins as drugs with intracellular targets. The mechanism by which proteins with transduction domains are taken up by cells and delivered to their targets is controversial but usually involves endocytosis. The effectiveness of transduced proteins may therefore be limited by their release from endosomes into the cytosol.

2 Originating Grant

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