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| Content Provider | Springer Nature Link |
|---|---|
| Author | Eeva, J. Pelkonen, J. |
| Copyright Year | 2004 |
| Abstract | B cell receptor (BCR)-mediated apoptosis plays a key role in the negative selection (deletion) of autoreactive B cells. Mechanisms of BCR-mediated apoptosis have been widely studied in cell lines representing both immature (bone marrow) and mature (germinal center) B cells. However, there is much inconsistency and controversy concerning the possible mechanisms of BCR-mediated apoptosis, which may reflect differences in the origin or the maturational stage of the cell line used. Based on recent studies, collapse of mitochondrial membrane potential (Δ Ψ m) seems to be an essential event for BCR-mediated apoptosis in both mature and immature cells. The collapse of Δ Ψ m is dependent on the synthesis of new proteins, which are involved in the permeability change of mitochondrial membranes. Mitochondrial dysfunction induces activation of caspases, cysteine proteases, which play a central role in apoptosis. However, instead of caspases, other effector proteases, such as cathepsins or calpains, may also be responsible for the organized destruction of cell components seen during BCR-mediated apoptosis. |
| Starting Page | 525 |
| Ending Page | 531 |
| Page Count | 7 |
| File Format | |
| ISSN | 13608185 |
| Journal | Apoptosis |
| Volume Number | 9 |
| Issue Number | 5 |
| e-ISSN | 1573675X |
| Language | English |
| Publisher | Kluwer Academic Publishers |
| Publisher Date | 2004-01-01 |
| Publisher Place | Boston |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Cancer Research Virology Anatomy Oncology Biochemistry |
| Content Type | Text |
| Resource Type | Article |
| Subject | Pharmaceutical Science Biochemistry (medical) Cell Biology Clinical Biochemistry Cancer Research Pharmacology |
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