The neuroprotective actions of FK506 binding protein ligands: neuronal survival is triggered by de novo RNA synthesis, but is independent of inhibition of JNK and calcineurin
| Autor: | A Klettner, Y Zhang, Ria Baumgrass, Gunter Fischer, Thomas Herdegen, E Bürger, K Mielke |
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| Rok vydání: | 2001 |
| Předmět: |
Cell Survival
Pyridines Calcineurin Inhibitors bcl-X Protein Apoptosis Nerve Tissue Proteins Caspase 3 Biology Ligands PC12 Cells Neuroprotection Tacrolimus Binding Proteins Cellular and Molecular Neuroscience Bcl-2-associated X protein Proto-Oncogene Proteins Animals Molecular Biology Nucleic Acid Synthesis Inhibitors bcl-2-Associated X Protein Neurons Reverse Transcriptase Polymerase Chain Reaction Activator (genetics) Effector Calcineurin JNK Mitogen-Activated Protein Kinases Hydrogen Peroxide Molecular biology Phosphoric Monoester Hydrolases Genes bcl-2 Rats Enzyme Activation Thiazoles Neuroprotective Agents FKBP Proto-Oncogene Proteins c-bcl-2 Enzyme inhibitor Caspases Dactinomycin biology.protein RNA Mitogen-Activated Protein Kinases |
| Zdroj: | Europe PubMed Central |
| ISSN: | 0169-328X |
| DOI: | 10.1016/s0169-328x(01)00286-8 |
| Popis: | The immunosuppressant FK506 displays substantial neuroprotective and neuroregenerative effects. It is not fully understood to which extent these effects depend on the inhibition of the calcineurin phosphatase (PP2B). The present study has re-addressed this issue using Lie120, a novel highly specific inhibitor of calcineurin, which does not block the enzymatic activity of FKBPs or cyclophilins, respectively. We have determined the effect of FK506 (10-500 nM), V-10,367 (a FK506 derivative which does not block calcineurin; 1-5 microM) and Lie120 (a novel specific inhibitor of calcineurin, 0.1-5 microM) on the cellular survival and the pro-degenerative JNK activity of PC12 and Neuro2A cells following application of 200 microM H(2)O(2). FK506 and V-10,367, but not Lie120, protected both cell lines against H(2)O(2)-mediated death, whereas an increase in JNK1 activity was blocked by FK506 and Lie120, but not by V-10,367. Co-incubation of FK506 and V-10,367 with the mRNA synthesis inhibitor actinomycin D abolished the protective effect of FK506 and V-10,367. This antagonization was effective when actinomycin D was applied 30 min or 1 h, but not 2 or 4 h, after H(2)O(2) suggesting that FKBP-ligands confer their neuroprotection by rapid de novo synthesis of (functionally) anti-apoptotic proteins. The search for the corresponding effector genes revealed that the expression of FKBP25, FKBP38 and FKBP52 (analysis by reverse transcription-polymerase chain reaction (RT-PCR) did not change following H(2)O(2) or FK506, and this was also true for the expression of apoptosis-related genes caspase 3, bax, bcl-2 and bcl-xL (analysis by Multiplex-PCR). Summarizing, neuronal protection by FKBP-ligands is not mediated either by calcineurin or by JNK1 in this experimental set-up, whereas the FK506 mediated inhibition of JNK1 is realized by the inhibition of calcineurin, an effective activator of JNK1 in neurons. |
| Databáze: | OpenAIRE |
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