دورية أكاديمية
G392E neuroserpin causing the dementia FENIB is secreted from cells but is not synaptotoxic
| العنوان: | G392E neuroserpin causing the dementia FENIB is secreted from cells but is not synaptotoxic |
|---|---|
| المؤلفون: | Ingwersen, T, Linnenberg, C, D'Acunto, E, Temori, S, Paolucci, I, Wasilewski, D, Mohammadi, B, Kirchmair, J, Glen, RC, Miranda, E, Glatzel, M, Galliciotti, G |
| المصدر: | 13 ; 1 |
| بيانات النشر: | Nature Publishing Group |
| سنة النشر: | 2021 |
| المجموعة: | Imperial College London: Spiral |
| مصطلحات موضوعية: | Science & Technology, Multidisciplinary Sciences, Science & Technology - Other Topics, TISSUE-PLASMINOGEN ACTIVATOR, FAMILIAL ENCEPHALOPATHY, Z ALPHA(1)-ANTITRYPSIN, INHIBITOR NEUROSERPIN, MUTANT NEUROSERPIN, POLYMERS, ACCUMULATION, DYSFUNCTION, PLASTICITY, Animals, Endoplasmic Reticulum, Golgi Apparatus, HEK293 Cells, Heredodegenerative Disorders, Nervous System, Hippocampus, Humans, Mice, Transgenic, Mutation, Neurons, Neuropeptides, Serpins, Synapses |
| الوصف: | Familial encephalopathy with neuroserpin inclusion bodies (FENIB) is a progressive neurodegenerative disease caused by point mutations in the gene for neuroserpin, a serine protease inhibitor of the nervous system. Different mutations are known that are responsible for mutant neuroserpin polymerization and accumulation as inclusion bodies in many cortical and subcortical neurons, thereby leading to cell death, dementia and epilepsy. Many efforts have been undertaken to elucidate the molecular pathways responsible for neuronal death. Most investigations have concentrated on analysis of intracellular mechanisms such as endoplasmic reticulum (ER) stress, ER-associated protein degradation (ERAD) and oxidative stress. We have generated a HEK-293 cell model of FENIB by overexpressing G392E-mutant neuroserpin and in this study we examine trafficking and toxicity of this polymerogenic variant. We observed that a small fraction of mutant neuroserpin is secreted via the ER-to-Golgi pathway, and that this release can be pharmacologically regulated. Overexpression of the mutant form of neuroserpin did not stimulate cell death in the HEK-293 cell model. Finally, when treating primary hippocampal neurons with G392E neuroserpin polymers, we did not detect cytotoxicity or synaptotoxicity. Altogether, we report here that a polymerogenic mutant form of neuroserpin is secreted from cells but is not toxic in the extracellular milieu. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | English |
| تدمد: | 2045-2322 |
| العلاقة: | Scientific Reports; http://hdl.handle.net/10044/1/93848Test |
| DOI: | 10.1038/s41598-021-88090-1 |
| الإتاحة: | https://doi.org/10.1038/s41598-021-88090-1Test http://hdl.handle.net/10044/1/93848Test |
| حقوق: | © The Author(s) 2021 ; http://creativecommons.org/licenses/by/4.0Test/ |
| رقم الانضمام: | edsbas.62919767 |
| قاعدة البيانات: | BASE |
Full Text Finder | تدمد: | 20452322 |
|---|---|
| DOI: | 10.1038/s41598-021-88090-1 |