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G392E neuroserpin causing the dementia FENIB is secreted from cells but is not synaptotoxic.
- Source :
-
Scientific reports [Sci Rep] 2021 Apr 22; Vol. 11 (1), pp. 8766. Date of Electronic Publication: 2021 Apr 22. - Publication Year :
- 2021
-
Abstract
- 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.
- Subjects :
- Animals
Endoplasmic Reticulum metabolism
Golgi Apparatus metabolism
HEK293 Cells
Hippocampus cytology
Hippocampus metabolism
Humans
Mice
Mice, Transgenic
Mutation
Neurons metabolism
Neuropeptides metabolism
Neuropeptides physiology
Serpins metabolism
Serpins physiology
Neuroserpin
Heredodegenerative Disorders, Nervous System metabolism
Neuropeptides genetics
Serpins genetics
Synapses pathology
Subjects
Details
- Language :
- English
- ISSN :
- 2045-2322
- Volume :
- 11
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Scientific reports
- Publication Type :
- Academic Journal
- Accession number :
- 33888787
- Full Text :
- https://doi.org/10.1038/s41598-021-88090-1