Desmin knockout muscles generate lower stress and are less vulnerable to injury compared with wild-type muscles.

The functional role of the skeletal muscle intermediate filament system was investigated by measuring the magnitude of muscle force loss after cyclic eccentric contraction (EC) in normal and desmin null mouse extensor digitorum longus muscles. Isometric stress generated was significantly greater in wild-type (313 +/- 8 kPa) compared with knockout muscles (276 +/- 13 kPa) before EC (P < 0.05), but 1 h after 10 ECs, both muscle types generated identical levels of stress ( approximately 250 kPa), suggesting less injury to the knockout. Differences in injury susceptibility were not explained by the different absolute stress levels imposed on wild-type versus knockout muscles (determined by testing older muscles) or by differences in fiber length or mechanical energy absorbed. Morphometric analysis of longitudinal electron micrographs indicated that Z disks from knockout muscles were more staggered (0.36 +/- 0. 03 microm) compared with wild-type muscles (0.22 +/- 0.03 microm), which may indicate that the knockout cytoskeleton is more compliant. These data demonstrate that lack of the intermediate filament system decreases isometric stress production and that the desmin knockout muscle is less vulnerable to mechanical injury.

[1]  L. Thornell,et al.  Null mutation in the desmin gene gives rise to a cardiomyopathy. , 1997, Journal of molecular and cellular cardiology.

[2]  F. Ren,et al.  Thermal stability of W ohmic contacts to n‐type GaN , 1996 .

[3]  E. Lazarides Intermediate filaments as mechanical integrators of cellular space , 1980, Nature.

[4]  M. Sjöström,et al.  Myofibrillar Damage Following Intense Eccentric Exercise in Man , 1983, International journal of sports medicine.

[5]  Y. Capetanaki,et al.  Disruption of muscle architecture and myocardial degeneration in mice lacking desmin , 1996, The Journal of cell biology.

[6]  R. Lieber,et al.  Relationship between muscle fiber types and sizes and muscle architectural properties in the mouse hindlimb , 1994, Journal of morphology.

[7]  M. Abraham,et al.  Oocyte maturation triggered by the presence of male in the Blue Gourami, Trichogaster trichopterus , 1994, Journal of morphology.

[8]  J. Friden,et al.  146 MUSCLE CYTOSKELETAL DISRUPTION OCCURS WITHIN THE FIRST 15 MINUTES OF CYCLIC ECCENTRIC CONTRACTION , 1994 .

[9]  R L Lieber,et al.  Muscle damage induced by eccentric contractions of 25% strain. , 1991, Journal of applied physiology.

[10]  D. K. Hill,et al.  Tension due to interaction between the sliding filaments in resting striated muscle. the effect of stimulation , 1968, The Journal of physiology.

[11]  Siegfried Labeit,et al.  Titins: Giant Proteins in Charge of Muscle Ultrastructure and Elasticity , 1995, Science.

[12]  E. Weibel Practical methods for biological morphometry , 1979 .

[13]  R. Armstrong,et al.  Eccentric exercise-induced injury to rat skeletal muscle. , 1983, Journal of applied physiology: respiratory, environmental and exercise physiology.

[14]  J A Faulkner,et al.  Injury to skeletal muscle fibers of mice following lengthening contractions. , 1985, Journal of applied physiology.

[15]  R. Armstrong,et al.  Excitation failure in eccentric contraction‐induced injury of mouse soleus muscle. , 1993, The Journal of physiology.

[16]  R L Lieber,et al.  Muscle cytoskeletal disruption occurs within the first 15 min of cyclic eccentric contraction. , 1996, Journal of applied physiology.

[17]  R. Lieber,et al.  Skeletal muscle architecture and fiber-type distribution with the multiple bellies of the mouse extensor digitorum longus muscle. , 1997, Acta anatomica.

[18]  K. Wang,et al.  Viscoelasticity of the sarcomere matrix of skeletal muscles. The titin-myosin composite filament is a dual-stage molecular spring. , 1993, Biophysical journal.

[19]  U. Proske,et al.  Effects of repeated eccentric contractions on structure and mechanical properties of toad sartorius muscle. , 1993, The American journal of physiology.

[20]  H. Sweeney,et al.  Dystrophin protects the sarcolemma from stresses developed during muscle contraction. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[21]  C. Babinet,et al.  Cardiovascular lesions and skeletal myopathy in mice lacking desmin. , 1996, Developmental biology.

[22]  R. Roy,et al.  Architecture of the hind limb muscles of cats: Functional significance , 1982, Journal of morphology.

[23]  G. Butler-Browne,et al.  Desmin Is Essential for the Tensile Strength and Integrity of Myofibrils but Not for Myogenic Commitment, Differentiation, and Fusion of Skeletal Muscle , 1997, The Journal of cell biology.

[24]  R. Walford When Is a Mouse “Old”? , 1976, The Journal of Immunology.

[25]  A. Keys,et al.  Density and composition of mammalian muscle , 1960 .