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Cytokine/chemokine profile in the skeletal muscle from chronic FSHD-like mice. Luminex protein quantification of cytokines/chemokines (A) eotaxin, (B) CXCL10, (C) CXCL1, (D) IL-2, (E) IL-12 (p40), (F) IL-12 (p70), and (G) VEGF in the <t>gastrocnemius</t> muscle of 3 month-old chronic FSHD-like mice. Luminex protein quantification of cytokines/chemokines (H) eotaxin, (I) CXCL10, (J) CCL2, (K) CCL3, (L) CXCL9, and (M) IL-6 in the gastrocnemius muscle of 6 month-old chronic FSHD-like mice. Luminex protein quantification of cytokines/chemokines (N) eotaxin, (O) IL-6, and (P) VEGF in the gastrocnemius muscle of 14–16 month-old chronic FSHD-like mice. Statistical analysis was performed using two-tailed Welch’s t-test. The numbers (n) are indicated as individual points in each graph. Protein levels below the detection threshold were removed from the analysis. Data are presented as mean ± s.e.m.; * P < 0.05, * * P < 0.01, * * * * P < 0.0001. Alt text: Greyscale figure with scatter plots showing cytokine/chemokine profiles from FSHD chronic mouse models.
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Cytokine/chemokine profile in the skeletal muscle from chronic FSHD-like mice. Luminex protein quantification of cytokines/chemokines (A) eotaxin, (B) CXCL10, (C) CXCL1, (D) IL-2, (E) IL-12 (p40), (F) IL-12 (p70), and (G) VEGF in the gastrocnemius muscle of 3 month-old chronic FSHD-like mice. Luminex protein quantification of cytokines/chemokines (H) eotaxin, (I) CXCL10, (J) CCL2, (K) CCL3, (L) CXCL9, and (M) IL-6 in the gastrocnemius muscle of 6 month-old chronic FSHD-like mice. Luminex protein quantification of cytokines/chemokines (N) eotaxin, (O) IL-6, and (P) VEGF in the gastrocnemius muscle of 14–16 month-old chronic FSHD-like mice. Statistical analysis was performed using two-tailed Welch’s t-test. The numbers (n) are indicated as individual points in each graph. Protein levels below the detection threshold were removed from the analysis. Data are presented as mean ± s.e.m.; * P < 0.05, * * P < 0.01, * * * * P < 0.0001. Alt text: Greyscale figure with scatter plots showing cytokine/chemokine profiles from FSHD chronic mouse models.

Journal: Human Molecular Genetics

Article Title: Muscle eosinophilia is a hallmark of chronic disease in facioscapulohumeral muscular dystrophy

doi: 10.1093/hmg/ddae019

Figure Lengend Snippet: Cytokine/chemokine profile in the skeletal muscle from chronic FSHD-like mice. Luminex protein quantification of cytokines/chemokines (A) eotaxin, (B) CXCL10, (C) CXCL1, (D) IL-2, (E) IL-12 (p40), (F) IL-12 (p70), and (G) VEGF in the gastrocnemius muscle of 3 month-old chronic FSHD-like mice. Luminex protein quantification of cytokines/chemokines (H) eotaxin, (I) CXCL10, (J) CCL2, (K) CCL3, (L) CXCL9, and (M) IL-6 in the gastrocnemius muscle of 6 month-old chronic FSHD-like mice. Luminex protein quantification of cytokines/chemokines (N) eotaxin, (O) IL-6, and (P) VEGF in the gastrocnemius muscle of 14–16 month-old chronic FSHD-like mice. Statistical analysis was performed using two-tailed Welch’s t-test. The numbers (n) are indicated as individual points in each graph. Protein levels below the detection threshold were removed from the analysis. Data are presented as mean ± s.e.m.; * P < 0.05, * * P < 0.01, * * * * P < 0.0001. Alt text: Greyscale figure with scatter plots showing cytokine/chemokine profiles from FSHD chronic mouse models.

Article Snippet: Muscle homogenates were prepared from freshly dissected gastrocnemius muscle as previously described [ ] with the sample-grinding kit (GE Healthcare Bio-Sciences, 80-6483-37), using half the volume of buffer recommended by the manufacturer [ ].

Techniques: Luminex, Two Tailed Test

Eosinophil activation in the skeletal muscle of chronic FSHD-like mice. Quantification of (A) eosinophil peroxidase (EPX), (B) eosinophil cationic protein (ECP), and (C) eosinophil-derived neurotoxin (EDN). Statistical analysis was performed with one-way ANOVA. EPX was quantified using n = 6 for 6 month-old ACTA1-MCM/+ , n = 8 for 6 month-old ACTA1-MCM/FLExD/+ , n = 8 for 14–18 month-old ACTA1-MCM/+ and n = 7 for 14–18 month-old ACTA1-MCM/FLExD/+ . ECP was quantified using n = 6 for 6 month-old ACTA1-MCM/+ , n = 8 for 6 month-old ACTA1-MCM/FLExD/+ , n = 8 for 14–18 month-old ACTA1-MCM/+ and n = 8 for 14–18 month-old ACTA1-MCM/FLExD/+ . EDN was quantified using n = 7 for 6 month-old ACTA1-MCM/+ , n = 8 for 6 month-old ACTA1-MCM/FLExD/+ , n = 8 for 14–18 month-old ACTA1-MCM/+ and n = 8 for 14–18 month-old ACTA1-MCM/FLExD/+ . Data are presented as mean ± s.e.m.; * P < 0.05, * * P < 0.01, * * * * P < 0.0001. Alt text: Greyscale scatter plots of the data from murine gastrocnemius muscle.

Journal: Human Molecular Genetics

Article Title: Muscle eosinophilia is a hallmark of chronic disease in facioscapulohumeral muscular dystrophy

doi: 10.1093/hmg/ddae019

Figure Lengend Snippet: Eosinophil activation in the skeletal muscle of chronic FSHD-like mice. Quantification of (A) eosinophil peroxidase (EPX), (B) eosinophil cationic protein (ECP), and (C) eosinophil-derived neurotoxin (EDN). Statistical analysis was performed with one-way ANOVA. EPX was quantified using n = 6 for 6 month-old ACTA1-MCM/+ , n = 8 for 6 month-old ACTA1-MCM/FLExD/+ , n = 8 for 14–18 month-old ACTA1-MCM/+ and n = 7 for 14–18 month-old ACTA1-MCM/FLExD/+ . ECP was quantified using n = 6 for 6 month-old ACTA1-MCM/+ , n = 8 for 6 month-old ACTA1-MCM/FLExD/+ , n = 8 for 14–18 month-old ACTA1-MCM/+ and n = 8 for 14–18 month-old ACTA1-MCM/FLExD/+ . EDN was quantified using n = 7 for 6 month-old ACTA1-MCM/+ , n = 8 for 6 month-old ACTA1-MCM/FLExD/+ , n = 8 for 14–18 month-old ACTA1-MCM/+ and n = 8 for 14–18 month-old ACTA1-MCM/FLExD/+ . Data are presented as mean ± s.e.m.; * P < 0.05, * * P < 0.01, * * * * P < 0.0001. Alt text: Greyscale scatter plots of the data from murine gastrocnemius muscle.

Article Snippet: Muscle homogenates were prepared from freshly dissected gastrocnemius muscle as previously described [ ] with the sample-grinding kit (GE Healthcare Bio-Sciences, 80-6483-37), using half the volume of buffer recommended by the manufacturer [ ].

Techniques: Activation Assay, Derivative Assay