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Image Search Results
Journal: bioRxiv
Article Title: GluN2D-containing NMDA receptors regulate dentate gyrus function by facilitating granule cell activity and mediating synaptic plasticity
doi: 10.64898/2026.03.06.710109
Figure Lengend Snippet: (A) Grin2d f l/fl mice were injected with AAV5-CamKII-mCherry (Control) or AAV-CamKII-mCherry-Cre ( Grin2d cKO). NMDAR-LTP was abolished in Grin2d cKO compared with control mice (Control: 149.5 ± 6.0 %, p < 0.01, n = 5, paired t-test; cKO: 92.5 ± 5.3 %, p = 0.12201, n = 6, paired t-test; Control vs cKO: p < 0.001, unpaired t-test). (B) WT mice were bilaterally injected with an anti-GluN2D antibody or control Ab into the dentate gyrus. After one hour, animals were euthanized, and slices were prepared. Injection was confirmed by the presence of methylene blue. NMDAR-LTP was abolished in mice injected with the anti-GluN2D antibody (cKO: 110.4 ± 8.5 %, p = 0.2952, n = 6, paired t-test) compared with control mice (Control: 149.8 ± 8.1 %, p < 0.001, n = 7, paired t-test; Control vs cKO: p < 0.01, unpaired t-test). (C) NMDAR-LTP was impaired in Grid1 KO mice (KO: 117.7 ± 5.3, p < 0.05%, n = 8, Wilcoxon signed-rank test) compared with controls (Control: 147.5 ± 6.7 %, p < 0.001, n = 7, paired t-test; Control vs cKO: p < 0.05, Mann-Whitney U test). Data are presented as mean ± s.e.m.
Article Snippet: For GluN2D cross-linking experiments in C57BL/6J, the control group received 1 μL of anti-rabbit Alexa 568 (control IgG, 1/5), while the GluN2D-cross-link group received 1 μg of
Techniques: Injection, Control, MANN-WHITNEY
Journal: The Journal of Neuroscience
Article Title: Nonionotropic Action of Endothelial NMDA Receptors on Blood–Brain Barrier Permeability via Rho/ROCK-Mediated Phosphorylation of Myosin
doi: 10.1523/JNEUROSCI.0969-19.2019
Figure Lengend Snippet: CNS endothelial NMDARs display the regulatory GluN2B and GluN3A subunits. Confocal photomicrographs represent coimmunostaining for the GluN1 subunit (anti-N-terminal domain; red) with the following regulatory NMDAR subunit (green): (A) Glun2B, GluN3A (corresponding 3D reconstruction in B), (C) GluN2A, GluN2C, GluN2D, and GluN3B in ECs of the mouse spinal cord. Yellow represents colocalizations. Scale bar, 10 μm.
Article Snippet: To analyze NMDAR subunits and tight junction proteins, the spinal cord tissue sample sections were incubated with the following primary antibodies: mouse monoclonal anti-GluN1 (Glunomab, 1:500) ( Lesept et al., 2016 ; Macrez et al., 2016 ), goat polyclonal anti-GluN2A (#1468, Santa Cruz Biotechnology, 1:200), rabbit polyclonal anti-GluN2B (#9057, Santa Cruz Biotechnology, 1:200), goat polyclonal anti-GluN2C (#1470, Santa Cruz Biotechnology, 1:200), goat polyclonal anti-GluN2D (#31551, Santa Cruz Biotechnology, 1:200),
Techniques:
Journal: The Journal of Neuroscience
Article Title: Nonionotropic Action of Endothelial NMDA Receptors on Blood–Brain Barrier Permeability via Rho/ROCK-Mediated Phosphorylation of Myosin
doi: 10.1523/JNEUROSCI.0969-19.2019
Figure Lengend Snippet: Inflammation-like conditions modulate the expression of NMDAR in hCMEC/D3 cells. A, Photomicrographs of hCMEC/D3 cells represent immunostaining for the NMDAR subunits GluN1, GluN2B, and GluN3A in control conditions or after TNF treatment (1 ng/ml). Scale bar, 20 μm. B, Corresponding quantification. Histograms represent mean ± SEM immunofluorescence. ****p < 0.0001. C, Immunoblotting against GluN1, GluN2B, and GluN3A of proteins extracted from hCMEC/D3 cells in control conditions or after TNF treatment and corresponding quantification. Histograms represent mean ± SEM (n = 3). *p < 0.05. **p < 0.01.
Article Snippet: To analyze NMDAR subunits and tight junction proteins, the spinal cord tissue sample sections were incubated with the following primary antibodies: mouse monoclonal anti-GluN1 (Glunomab, 1:500) ( Lesept et al., 2016 ; Macrez et al., 2016 ), goat polyclonal anti-GluN2A (#1468, Santa Cruz Biotechnology, 1:200), rabbit polyclonal anti-GluN2B (#9057, Santa Cruz Biotechnology, 1:200), goat polyclonal anti-GluN2C (#1470, Santa Cruz Biotechnology, 1:200), goat polyclonal anti-GluN2D (#31551, Santa Cruz Biotechnology, 1:200),
Techniques: Expressing, Immunostaining, Immunofluorescence, Western Blot