Skip to main content
. 2011 Jan 5;300(4):C803–C813. doi: 10.1152/ajpcell.00394.2010

Fig. 2.

Fig. 2.

Ultrastructural studies of TA muscles lacking desmin, K19, or both proteins. Micrographs show representative transmission electron microscopic images of longitudinal sections of TA muscles from WT (A), K19−/− (B), desmin−/− (C), and DKO (D) mice. Scale bar in D applies to A–D (0.5 μm). E: compared with WT muscles, all 3 mutants showed a significant increase in the distance between the outermost myofibrils and the sarcolemma (Z line to membrane distance), with the largest in K19−/− muscles. The absence of desmin in the DKO muscle reduces this distance to a value identical to that seen in desmin−/− muscle. F: sarcomere alignment was determined by the horizontal distance from 1 Z line to the Z line in an adjacent myofibril (Z line to Z line distance). The sarcomeres were not significantly displaced in K19−/− compared with WT muscles, but the displacement increased significantly in the desmin−/− and was greatest in DKO muscles. *P < 0.001. G: quantitation of mitochondria under sarcolemma. The fraction of cytoplasmic surface of the sarcolemmal membrane covered by mitochondria (at levels of <10%, 10–50%, or >50%) was recorded. The large increase in subsarcolemmal mitochondria in the K19-null mouse and the smaller increase in the desmin-null mouse are absent in the DKO mouse.