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Research ArticleResearch Article: New Research, Disorders of the Nervous System

Sex-Specific Differences in Motor-Unit Remodeling in a Mouse Model of ALS

Éric Martineau, Adriana Di Polo, Christine Vande Velde and Richard Robitaille
eNeuro 7 February 2020, 7 (1) ENEURO.0388-19.2020; https://doi.org/10.1523/ENEURO.0388-19.2020
Éric Martineau
1Département de neurosciences, Université de Montréal, Montréal, Québec H3C 3J7, Canada
2Centre de Recherche du Centre Hospitalier Universitaire Sainte-Justine, Montréal, Québec H3T 1C5, Canada
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Adriana Di Polo
1Département de neurosciences, Université de Montréal, Montréal, Québec H3C 3J7, Canada
3Centre de Recherche du Centre Hospitalier de l’Université de Montréal, Montréal, Québec H2X 0A9, Canada
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Christine Vande Velde
1Département de neurosciences, Université de Montréal, Montréal, Québec H3C 3J7, Canada
3Centre de Recherche du Centre Hospitalier de l’Université de Montréal, Montréal, Québec H2X 0A9, Canada
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Richard Robitaille
1Département de neurosciences, Université de Montréal, Montréal, Québec H3C 3J7, Canada
4Groupe de Recherche sur le Système Nerveux Central, Université de Montréal, Montréal, Québec, H3C 1J7, Canada
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  • Figure 1.
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    Figure 1.

    Sex-specific differences in MU dynamics in SOD1G37R/YFP mice. A, Examples of MU arbors from a male and a female SOD1/YFP mice during three sessions (male: session 2, 3, and 5; female: session 2, 4, and 5), with higher magnification on-focus insets of NMJs of interest (digital zoom, dashed box in low magnification). Green: YFP-labeled axon; red: nAChR. Note how the imaged motor axon retracted from two NMJs (arrowheads) between sessions 3 and 5 in the male example. Furthermore, note the formation of a new axonal branch between sessions 2 and 4 in the female example (arrow), innervating an NMJ that previously did not belong to this MU (MU expansion). B, MU dynamic diagram of the MUs shown in A, showing that MU are much more likely to expand in female SOD1G37R/YFP mice. Black lines represent the axonal arborization and each box represents a single NMJ. Note how asynchronous NMJ losses occurred in both these MUs, but how partial losses seem more frequent in the male MU. C, D, Histograms showing the average proportion of NMJs from the initial pool which are innervated (green), re-innervated (purple), or lost (red) by the MU and the proportion which are gained (blue) for female (C) and male (D) SOD1G37R/YFP mice. Numbers in the histogram bars represent the number of remaining MU arbors (those which did not globally degenerate) over the total number of MUs observed. Again, note how MU expansions are more frequent in female than in male mice. Scale bar: 100 μm (low magnification) and 25 μm (high magnification).

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    Figure 2.

    Motor function declines slightly faster in female SOD1G37R/YFP mice. A, B, Body weight (A) and all-limb grip strength (B) curves of male and female (light and dark colors, respectively) WT/YFP and SOD1G37R/YFP mice (blue and red, respectively) during the symptomatic stages (WT female: N = 14; WT male: N = 6; SOD1 female: N = 8; SOD1 male: N = 12). Data are presented as mean ± SEM. Main effects and interactions are reported in Table 1 and in the text. Asterisks and crosses represent biologically relevant statistically significant differences in the post hoc test (Tukey’s multiple comparisons). Asterisks represent differences compared with the other genotype, while crosses represent differences compared with the other sex; */†p < 0.05, **/††p < 0.01, ***/†††p < 0.001, ****/††††p < 0.0001.

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    Figure 3.

    α-motor neuron loss and NMJ denervation are slightly more pronounced in female SOD1G37R/YFP mice at P360. A, Representative image of lumbar spinal cord sections from a female WT/YFP mice at P360 (red: ChAT; blue: NeuN; green: YFP). B, Representative image of NMJs in the tibialis anterior muscle of a female WT/YFP mice at P360 (red: α-BTX; green: NF-M and SV2). C, Representative examples of lumbar spinal cord sections from female (top) and male (bottom) SOD1G37R/YFP mice at P360. D, Representative images of NMJs in the tibialis anterior muscle of female (top) and male (bottom) SOD1G37R/YFP mice at P360. E, F, Quantification of the number of α-motor neurons (E, ChAT+ NeuN+ cells) and γ-motor neurons (F, ChAT+ NeuN– cells) per ventral horn at P360 (WT female: N = 4; WT male: N = 2; SOD1 female: N = 4; SOD1 male: N = 5). G, Quantification of the percentage of fully innervated NMJs in the tibialis anterior at P360 (WT female: N = 4, n = 1078; WT male: N = 2, n = 446; SOD1 female: N = 4, n = 977; SOD1 male: N = 5, n = 820). Data are presented as mean ± SEM. Main effects and interactions are reported in Table 2 and in the text. Asterisks represent biologically relevant statistically significant differences in the post hoc test (E, F, Tukey’s multiple comparisons; G, Holm–Sidak’s correction); *p < 0.05, **p < 0.01, ***p < 0.001. Scale bar: 100 μm.

Tables

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    Table 1

    Effect of time, sex, and genotype on disease progression in SOD1G37R mice

    AnalysisStatistical testMain effectp value
    Body weight (Fig. 2A)RM three-way ANOVATime<0.001***
    Genotype<0.001***
    Sex<0.001***
    Time × genotype<0.001***
    Time × sex0.854
    Sex × genotype0.868
    Time × sex × genotype0.397
    Grip strength (Fig. 2B)RM three-way ANOVATime<0.001***
    Genotype<0.001***
    Sex<0.001***
    Time × genotype<0.001***
    Time × sex0.007**
    Sex × genotype0.023*
    Time × sex × genotype0.011*
    • Bold values represent statistically significant differences (p < 0.05).

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    Table 2

    Effect of sex and genotype on neuronal survival and NMJ innervation in SOD1G37R mice

    AnalysisStatistical TestMain effectp value
    α-Motor neurons counts
    (Fig. 3E)
    Two-way ANOVAGenotype<0.001***
    Sex0.002**
    Sex × genotype0.941
    γ-Motor neurons counts
    (Fig. 3F)
    Two-way ANOVAGenotype0.673
    Sex0.042*
    Sex × genotype0.365
    NMJ innervation
    (Fig. 3G)
    GLM, logistic distributionGenotype<0.001***
    Sex0.431
    Sex × genotype0.019*
    • Bold values represent statistically significant differences (p < 0.05).

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Sex-Specific Differences in Motor-Unit Remodeling in a Mouse Model of ALS
Éric Martineau, Adriana Di Polo, Christine Vande Velde, Richard Robitaille
eNeuro 7 February 2020, 7 (1) ENEURO.0388-19.2020; DOI: 10.1523/ENEURO.0388-19.2020

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Sex-Specific Differences in Motor-Unit Remodeling in a Mouse Model of ALS
Éric Martineau, Adriana Di Polo, Christine Vande Velde, Richard Robitaille
eNeuro 7 February 2020, 7 (1) ENEURO.0388-19.2020; DOI: 10.1523/ENEURO.0388-19.2020
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Keywords

  • amyotrophic lateral sclerosis
  • motor-unit
  • neuromuscular junction
  • reinnervation
  • sex-specific differences
  • superoxide dismutase

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