Anti-NMDAR1 antibody impairs dendritic branching in immature cultured neurons
Language English Country Poland Media print-electronic
Document type Journal Article
Grant support
GAUK 365121
Charles University - Czech Republic
PubMed
39434510
DOI
10.32725/jab.2024.019
Knihovny.cz E-resources
- Keywords
- Anti-NMDAR encephalitis, BDNF, Dendritic branching, Neuronal development, Synaptic proteins,
- MeSH
- Dendrites * drug effects metabolism MeSH
- Rats MeSH
- Cells, Cultured MeSH
- Membrane Proteins metabolism immunology MeSH
- Brain-Derived Neurotrophic Factor * metabolism MeSH
- Neurons * metabolism drug effects MeSH
- Disks Large Homolog 4 Protein metabolism MeSH
- Nerve Tissue Proteins immunology metabolism MeSH
- Receptors, N-Methyl-D-Aspartate * immunology MeSH
- Synaptophysin metabolism MeSH
- Carrier Proteins MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- gephyrin MeSH Browser
- Membrane Proteins MeSH
- Brain-Derived Neurotrophic Factor * MeSH
- Disks Large Homolog 4 Protein MeSH
- Nerve Tissue Proteins MeSH
- Receptors, N-Methyl-D-Aspartate * MeSH
- Synaptophysin MeSH
- Carrier Proteins MeSH
Anti-N-methyl D-aspartate receptor (anti-NMDAR) encephalitis is an autoimmune disorder characterized by IgG antibodies targeting NMDAR. The prevalence is remarkably higher in women and some develop the condition during pregnancy. While immunotherapies have shown good outcomes for pregnant mothers and their infants, the impact on early neurodevelopment remains elusive. This study investigates the effects of anti-NMDAR antibody on the development of primary cortical cultures. Anti-NMDAR antibody was administered to the cultures at day in vitro 5 for the following 5 days to assess dendritic branching and arbor complexity, and at day in vitro 14 for measuring the expression of brain-derived neurotrophic factor (BDNF) and synaptic proteins. Immature cultured neurons treated with anti-NMDAR antibody exhibited impaired dendritic branching and arbor complexity. Interestingly, BDNF expression was unaffected in mature neurons. Additionally, GluN1 expression, a mandatory NMDAR subunit, was significantly reduced, while no significant alterations were observed in PSD-95, gephyrin and synaptophysin expression. These findings shed light on the structural and synaptic impacts of anti-NMDAR antibody on immature neurons, providing evidence for their consequences in early neuronal development.
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