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. Author manuscript; available in PMC: 2019 May 29.
Published in final edited form as: Genes Brain Behav. 2018 Nov 6;18(1):e12526. doi: 10.1111/gbb.12526

TABLE 2.

Summary of significant effects of genotype on dendrite morphology

Brain region of neurons Morphology parameter Sex Genotypes Change from WT, % Genotypes Change from T4826I, % Genotypes Change from DM, %
Hippocampal Distance from soma of peak # intersections (μm) Male WT vs T4826I 31.73% increase DM vs 48261 25.28% increase
Hippocampal Number of primary dendrites/neuron Male WT vs T4826I 20.68% decrease T4826I vs CGG 35.35% increase DM vs CGG 21.85% increase
Hippocampal # Dendritic tips/neuron Male WT vs CGG 24.67% increase T4826I vs CGG 17.72% increase DM vs CGG 27.77% increase
Hippocampal Tips/primary dendrite Male WT vs T4826I 46.49% increase
Hippocampal Mean dendritic length (μm) Male WT vs T4826I 41.23% increase
Hippocampal Soma area (μm2) Female WT vs CGG 22.87 % increase T4826I vs CGG 20.81% increase DM vs CGG 27.5% increase
Hippocampal Soma area (μm2) Male T4826I vs CGG 18.89% increase DM vs CGG 25.39% increase
Cortical Distance from soma of peak # intersections (μm) Female T4826I vs CGG
T4826I vs DM
16.36% increase
17.5% increase
Cortical Distance from soma of peak # intersections (μm) Male WT vs CGG 16.75% increase
Cortical # Intersections at peak Female T4826I vs CGG 17.94% increase
Cortical Area under sholl curve Female T4826I vs DM 29.99% increase
Cortical Distal area under sholl cuve Female WT vs DM 22.84% increase
Cortical # Dendritic tips/neuron Female WT vs DM 19.79% increase T4826I vs DM 23.03% increase
Cortical Tips/primary dendrite Male WT vs DM 17.22% increase T4826I vs DM 18.42% increase
Cortical Tips/primary dendrite Female WT vs DM
WT vs CGG
32.07% increase
23.33% increase
T4826I vs DM 23.38% increase
Cortical Mean dendritic length (μm) Female WT vs DM 47.42% increase T4826I vs DM 40.85% increase

Abbreviations: CGG, mice expressing a CGG repeat expansion in the fragile X mental retardation 1 gene; DM, double mutation (CGG+T4826I); T4826I, T4826I-ryanodine receptor 1 mutation; WT, wild-type.