SRF mediates activity-induced gene expression and synaptic plasticity but not neuronal viability

التفاصيل البيبلوغرافية
العنوان: SRF mediates activity-induced gene expression and synaptic plasticity but not neuronal viability
المؤلفون: Ying Shen, Sarah Sarsfield, Thomas Lemberger, Günther Schütz, Narendrakumar Ramanan, David D. Ginty, David J. Linden
المصدر: Nature Neuroscience. 8:759-767
بيانات النشر: Springer Science and Business Media LLC, 2005.
سنة النشر: 2005
مصطلحات موضوعية: Transcriptional Activation, Serum Response Factor, Cell Survival, MAP Kinase Signaling System, Long-Term Potentiation, Presynaptic Terminals, Nonsynaptic plasticity, Biology, CREB, Hippocampus, Synaptic Transmission, Mice, Organ Culture Techniques, Serum response factor, Metaplasticity, Animals, Cyclic AMP Response Element-Binding Protein, Genes, Immediate-Early, Neuronal memory allocation, Mice, Knockout, Neuronal Plasticity, Pyramidal Cells, General Neuroscience, Long-term potentiation, Mice, Mutant Strains, Synaptic fatigue, Gene Expression Regulation, Synaptic plasticity, biology.protein, Neuroscience, Signal Transduction
الوصف: Synaptic activity-dependent gene expression is critical for certain forms of neuronal plasticity and survival in the mammalian nervous system, yet the mechanisms by which coordinated regulation of activity-induced genes supports neuronal function is unclear. Here, we show that deletion of serum response factor (SRF) in specific neuronal populations in adult mice results in profound deficits in activity-dependent immediate early gene expression, but components of upstream signaling pathways and cyclic AMP-response element binding protein (CREB)-dependent transactivation remain intact. Moreover, SRF-deficient CA1 pyramidal neurons show attenuation of long-term synaptic potentiation, a model for neuronal information storage. Furthermore, in contrast to the massive neurodegeneration seen in adult mice lacking CREB family members, SRF-deficient adult neurons show normal morphologies and basal excitatory synaptic transmission. These findings indicate that the transcriptional events underlying neuronal survival and plasticity are dissociable and that SRF plays a prominent role in use-dependent modification of synaptic strength in the adult brain.
تدمد: 1546-1726
1097-6256
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b0ce1d74f20353f2b33045bb4ba98bbTest
https://doi.org/10.1038/nn1462Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....9b0ce1d74f20353f2b33045bb4ba98bb
قاعدة البيانات: OpenAIRE