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Mitral cells are susceptible to neuroinflammation in EAE. A Representative immunofluorescence image and quantification of reelin-positive mitral cells per mm mitral cell layer (MCL) and glomerular layer (GL) in healthy mice and mice at acute EAE (d15 p.i.) (MC: n = 8 per group; GL: n = 7 per group). Scale bars = 100 µm. B Representative images and quantification of phosphorylated (SMI31) and non- phosphorylated <t>(SMI32)</t> neurofilaments measured by mean fluorescence intensity (MFI) in the internal plexiform layer (IPL) of healthy ( n = 10) and EAE animals ( n = 9 per group). Scale bars = 100 µm. C Visualization and quantification of the synaptic density in the external plexiform layer measured by positive particles per area in mm 2 of postsynaptic density protein PSD95 and presynaptic protein synapsin 1 (Syn1), as well as the colocalization of both, with latter corresponding to synapses between mitral cells and granular cells, in healthy animals, in onset EAE (d10 p.i.), acute EAE (d15 p.i.) and chronic EAE (d30 p.i.) ( n = 5–7 per group). Scale bars = 20 µm. Bars show mean values ± s.e.m. Statistical analysis was performed one-way ANOVA followed by Tukey’s post hoc test; * P < 0.05, ** P < 0.01, *** P < 0.001
Purified Anti Neurofilament H (Nf H) Monoclonal Mouse Smi31 Antibody, supplied by Sternberger Monoclonals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Mitral cells are susceptible to neuroinflammation in EAE. A Representative immunofluorescence image and quantification of reelin-positive mitral cells per mm mitral cell layer (MCL) and glomerular layer (GL) in healthy mice and mice at acute EAE (d15 p.i.) (MC: n = 8 per group; GL: n = 7 per group). Scale bars = 100 µm. B Representative images and quantification of phosphorylated (SMI31) and non- phosphorylated <t>(SMI32)</t> neurofilaments measured by mean fluorescence intensity (MFI) in the internal plexiform layer (IPL) of healthy ( n = 10) and EAE animals ( n = 9 per group). Scale bars = 100 µm. C Visualization and quantification of the synaptic density in the external plexiform layer measured by positive particles per area in mm 2 of postsynaptic density protein PSD95 and presynaptic protein synapsin 1 (Syn1), as well as the colocalization of both, with latter corresponding to synapses between mitral cells and granular cells, in healthy animals, in onset EAE (d10 p.i.), acute EAE (d15 p.i.) and chronic EAE (d30 p.i.) ( n = 5–7 per group). Scale bars = 20 µm. Bars show mean values ± s.e.m. Statistical analysis was performed one-way ANOVA followed by Tukey’s post hoc test; * P < 0.05, ** P < 0.01, *** P < 0.001
Sternberger® Purified Anti Neurofilament H (Nf H) Monoclonal Mouse Smi32 Antibody, supplied by Sternberger Monoclonals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Mitral cells are susceptible to neuroinflammation in EAE. A Representative immunofluorescence image and quantification of reelin-positive mitral cells per mm mitral cell layer (MCL) and glomerular layer (GL) in healthy mice and mice at acute EAE (d15 p.i.) (MC: n = 8 per group; GL: n = 7 per group). Scale bars = 100 µm. B Representative images and quantification of phosphorylated (SMI31) and non- phosphorylated <t>(SMI32)</t> neurofilaments measured by mean fluorescence intensity (MFI) in the internal plexiform layer (IPL) of healthy ( n = 10) and EAE animals ( n = 9 per group). Scale bars = 100 µm. C Visualization and quantification of the synaptic density in the external plexiform layer measured by positive particles per area in mm 2 of postsynaptic density protein PSD95 and presynaptic protein synapsin 1 (Syn1), as well as the colocalization of both, with latter corresponding to synapses between mitral cells and granular cells, in healthy animals, in onset EAE (d10 p.i.), acute EAE (d15 p.i.) and chronic EAE (d30 p.i.) ( n = 5–7 per group). Scale bars = 20 µm. Bars show mean values ± s.e.m. Statistical analysis was performed one-way ANOVA followed by Tukey’s post hoc test; * P < 0.05, ** P < 0.01, *** P < 0.001
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Mitral cells are susceptible to neuroinflammation in EAE. A Representative immunofluorescence image and quantification of reelin-positive mitral cells per mm mitral cell layer (MCL) and glomerular layer (GL) in healthy mice and mice at acute EAE (d15 p.i.) (MC: n = 8 per group; GL: n = 7 per group). Scale bars = 100 µm. B Representative images and quantification of phosphorylated (SMI31) and non- phosphorylated <t>(SMI32)</t> neurofilaments measured by mean fluorescence intensity (MFI) in the internal plexiform layer (IPL) of healthy ( n = 10) and EAE animals ( n = 9 per group). Scale bars = 100 µm. C Visualization and quantification of the synaptic density in the external plexiform layer measured by positive particles per area in mm 2 of postsynaptic density protein PSD95 and presynaptic protein synapsin 1 (Syn1), as well as the colocalization of both, with latter corresponding to synapses between mitral cells and granular cells, in healthy animals, in onset EAE (d10 p.i.), acute EAE (d15 p.i.) and chronic EAE (d30 p.i.) ( n = 5–7 per group). Scale bars = 20 µm. Bars show mean values ± s.e.m. Statistical analysis was performed one-way ANOVA followed by Tukey’s post hoc test; * P < 0.05, ** P < 0.01, *** P < 0.001
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Mitral cells are susceptible to neuroinflammation in EAE. A Representative immunofluorescence image and quantification of reelin-positive mitral cells per mm mitral cell layer (MCL) and glomerular layer (GL) in healthy mice and mice at acute EAE (d15 p.i.) (MC: n = 8 per group; GL: n = 7 per group). Scale bars = 100 µm. B Representative images and quantification of phosphorylated (SMI31) and non- phosphorylated <t>(SMI32)</t> neurofilaments measured by mean fluorescence intensity (MFI) in the internal plexiform layer (IPL) of healthy ( n = 10) and EAE animals ( n = 9 per group). Scale bars = 100 µm. C Visualization and quantification of the synaptic density in the external plexiform layer measured by positive particles per area in mm 2 of postsynaptic density protein PSD95 and presynaptic protein synapsin 1 (Syn1), as well as the colocalization of both, with latter corresponding to synapses between mitral cells and granular cells, in healthy animals, in onset EAE (d10 p.i.), acute EAE (d15 p.i.) and chronic EAE (d30 p.i.) ( n = 5–7 per group). Scale bars = 20 µm. Bars show mean values ± s.e.m. Statistical analysis was performed one-way ANOVA followed by Tukey’s post hoc test; * P < 0.05, ** P < 0.01, *** P < 0.001
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mouse monoclonal anti neurofilament heavy chain nf h  (Santa Cruz Biotechnology)
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Mitral cells are susceptible to neuroinflammation in EAE. A Representative immunofluorescence image and quantification of reelin-positive mitral cells per mm mitral cell layer (MCL) and glomerular layer (GL) in healthy mice and mice at acute EAE (d15 p.i.) (MC: n = 8 per group; GL: n = 7 per group). Scale bars = 100 µm. B Representative images and quantification of phosphorylated (SMI31) and non- phosphorylated <t>(SMI32)</t> neurofilaments measured by mean fluorescence intensity (MFI) in the internal plexiform layer (IPL) of healthy ( n = 10) and EAE animals ( n = 9 per group). Scale bars = 100 µm. C Visualization and quantification of the synaptic density in the external plexiform layer measured by positive particles per area in mm 2 of postsynaptic density protein PSD95 and presynaptic protein synapsin 1 (Syn1), as well as the colocalization of both, with latter corresponding to synapses between mitral cells and granular cells, in healthy animals, in onset EAE (d10 p.i.), acute EAE (d15 p.i.) and chronic EAE (d30 p.i.) ( n = 5–7 per group). Scale bars = 20 µm. Bars show mean values ± s.e.m. Statistical analysis was performed one-way ANOVA followed by Tukey’s post hoc test; * P < 0.05, ** P < 0.01, *** P < 0.001
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Mitral cells are susceptible to neuroinflammation in EAE. A Representative immunofluorescence image and quantification of reelin-positive mitral cells per mm mitral cell layer (MCL) and glomerular layer (GL) in healthy mice and mice at acute EAE (d15 p.i.) (MC: n = 8 per group; GL: n = 7 per group). Scale bars = 100 µm. B Representative images and quantification of phosphorylated (SMI31) and non- phosphorylated <t>(SMI32)</t> neurofilaments measured by mean fluorescence intensity (MFI) in the internal plexiform layer (IPL) of healthy ( n = 10) and EAE animals ( n = 9 per group). Scale bars = 100 µm. C Visualization and quantification of the synaptic density in the external plexiform layer measured by positive particles per area in mm 2 of postsynaptic density protein PSD95 and presynaptic protein synapsin 1 (Syn1), as well as the colocalization of both, with latter corresponding to synapses between mitral cells and granular cells, in healthy animals, in onset EAE (d10 p.i.), acute EAE (d15 p.i.) and chronic EAE (d30 p.i.) ( n = 5–7 per group). Scale bars = 20 µm. Bars show mean values ± s.e.m. Statistical analysis was performed one-way ANOVA followed by Tukey’s post hoc test; * P < 0.05, ** P < 0.01, *** P < 0.001
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Mitral cells are susceptible to neuroinflammation in EAE. A Representative immunofluorescence image and quantification of reelin-positive mitral cells per mm mitral cell layer (MCL) and glomerular layer (GL) in healthy mice and mice at acute EAE (d15 p.i.) (MC: n = 8 per group; GL: n = 7 per group). Scale bars = 100 µm. B Representative images and quantification of phosphorylated (SMI31) and non- phosphorylated (SMI32) neurofilaments measured by mean fluorescence intensity (MFI) in the internal plexiform layer (IPL) of healthy ( n = 10) and EAE animals ( n = 9 per group). Scale bars = 100 µm. C Visualization and quantification of the synaptic density in the external plexiform layer measured by positive particles per area in mm 2 of postsynaptic density protein PSD95 and presynaptic protein synapsin 1 (Syn1), as well as the colocalization of both, with latter corresponding to synapses between mitral cells and granular cells, in healthy animals, in onset EAE (d10 p.i.), acute EAE (d15 p.i.) and chronic EAE (d30 p.i.) ( n = 5–7 per group). Scale bars = 20 µm. Bars show mean values ± s.e.m. Statistical analysis was performed one-way ANOVA followed by Tukey’s post hoc test; * P < 0.05, ** P < 0.01, *** P < 0.001

Journal: Journal of Neuroinflammation

Article Title: Neuroinflammation causes mitral cell dysfunction and olfactory impairment in a multiple sclerosis model

doi: 10.1186/s12974-025-03388-5

Figure Lengend Snippet: Mitral cells are susceptible to neuroinflammation in EAE. A Representative immunofluorescence image and quantification of reelin-positive mitral cells per mm mitral cell layer (MCL) and glomerular layer (GL) in healthy mice and mice at acute EAE (d15 p.i.) (MC: n = 8 per group; GL: n = 7 per group). Scale bars = 100 µm. B Representative images and quantification of phosphorylated (SMI31) and non- phosphorylated (SMI32) neurofilaments measured by mean fluorescence intensity (MFI) in the internal plexiform layer (IPL) of healthy ( n = 10) and EAE animals ( n = 9 per group). Scale bars = 100 µm. C Visualization and quantification of the synaptic density in the external plexiform layer measured by positive particles per area in mm 2 of postsynaptic density protein PSD95 and presynaptic protein synapsin 1 (Syn1), as well as the colocalization of both, with latter corresponding to synapses between mitral cells and granular cells, in healthy animals, in onset EAE (d10 p.i.), acute EAE (d15 p.i.) and chronic EAE (d30 p.i.) ( n = 5–7 per group). Scale bars = 20 µm. Bars show mean values ± s.e.m. Statistical analysis was performed one-way ANOVA followed by Tukey’s post hoc test; * P < 0.05, ** P < 0.01, *** P < 0.001

Article Snippet: For staining of neurofilaments in the IPL of olfactory bulb slices we used Sternberger® purified anti-neurofilament H (NF-H) monoclonal mouse SMI31 and SMI32 antibodies to detect phosphorylated and non-phosphorylated neurofilament H, respectively.

Techniques: Immunofluorescence, Fluorescence