Skip to main content
Fig. 1 | Acta Neuropathologica Communications

Fig. 1

From: Myopathologic trajectory in Duchenne muscular dystrophy (DMD) reveals lack of regeneration due to senescence in satellite cells

Fig. 1

Characterization of DMD muscle phenotype. a Hematoxylin & Eosin (H&E) staining of Control (Ctr) and DMD muscles at different time points. Blue arrows represent necrotic fibers. Black stars represent hypercontracted fibers (scale bar = 50 μm). b Histopathologic index calculated on H&E stainings of Ctr and DMD biopsies at different time points. c Quantification of necrotic fibers of Ctr and DMD muscle from H&E. d Quantification of fibers with internalized nuclei on DMD and control biopsies at different time points. e Quantification of hypercontracted fibers on DMD and Ctr biopsies. f Representative immunofluorescence for CD45 (red), Laminin (green) in Ctr and DMD quadriceps at 7 years. Nuclei are counterstained with DAPI (blue) (scale bar = 20 μm). g) Quantification of inflammatory cells CD45-positive per mm2 in DMD and Ctr biopsies at different time points. Pvalues were calculated by Mann–Whitney tests comparing control and DMD groups within the same age range

Back to article page