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. 2018 Nov 30;9:5104. doi: 10.1038/s41467-018-07639-3

Fig. 6.

Fig. 6

Cysteine 272 of γcyto-actin is necessary for protection of mdx muscle from eccentric contraction-induced force loss. a Immunoblot comparison of γcyto (Actg1-TG), γcytoC272A (C272A-TG), and βcyto (Actb-TG) overexpression in mdx gastrocnemius muscle. b Immunofluorescence analysis demonstrates similar distributions of γcyto, γcytoC272A, and βcyto in 10 µm quadriceps cryosections. Scale bar = 50 µm. c EDL muscles isolated from WT, mdx, mdx/Actg1-TG, mdx/C272A-TG, and mdx/Actb-TG mice were subjected to 10 eccentric contractions and the forces measured expressed as a percentage of the force generated during the first eccentric contraction; n = 8 for WT and mdx/C272A-TG; n = 5 for mdx; n = 6 for mdx/Actg1-TG and mdx/Actb-TG. *The mdx/Actg1-TG significantly different from mdx (P ≤ 0.05), #mdx/Actb-TG significantly different from mdx (P ≤ 0.05); two-way ANOVA. d Rate of DCF fluorescence in single flexor digitorum brevis (FDB) muscles from WT, mdx, mdx/Actg1-TG, mdx/C272A-TG, and mdx/Actb-TG mice exposed to cyclic stretch in the presence of DMSO (vehicle) or the NOX2 inhibitor gp91ds-tat; n = 9 for WT, mdx/Actg1-TG, and mdx/Actb-TG; n = 12 for mdx; n = 7 for mdx/C272A-TG. ***P < 0.001, ns no significance compared to WT; one-way ANOVA. Throughout, error bars represent means ± SEM