Inhibition of Mitochondrial Neural Cell Death Pathways by Protein Transduction of Bcl-2 Family Proteins
Autor: | Lucian Soane, Gary Fiskum |
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Rok vydání: | 2005 |
Předmět: |
Cell Survival
Physiology Endosome Apoptosis Mitochondrion Endocytosis Article Transduction (genetics) Bcl-2-associated X protein Transduction Genetic Animals Humans bcl-2-Associated X Protein Neurons biology Bcl-2 family Cytochromes c Cell Biology Mitochondria Cell biology Cytosol Proto-Oncogene Proteins c-bcl-2 Biochemistry Mitochondrial Membranes biology.protein Signal transduction Reactive Oxygen Species Heparan Sulfate Proteoglycans Signal Transduction |
Zdroj: | Journal of Bioenergetics and Biomembranes. 37:179-190 |
ISSN: | 1573-6881 0145-479X |
DOI: | 10.1007/s10863-005-6590-8 |
Popis: | 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. |
Databáze: | OpenAIRE |
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