Structural and functional evaluation of branched myofibers lacking intermediate filaments

American Journal of Physiology - Cell Physiology

Volumn 303, Issue 2, 2012, Pages

  Goodall, Mariah H ^a   Ward, Christopher W ^b   Pratt, Stephen J P ^a   Bloch, Robert J ^a   Lovering, Richard M ^a  

^a UNIVERSITY OF MARYLAND SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF MARYLAND SCHOOL OF NURSING   (United States)

Author keywords

Calcium; Muscular dystrophy; Skeletal muscle

Indexed keywords

CALCIUM ION; CYTOKERATIN 19; DESMIN;

ANIMAL EXPERIMENT; ARTICLE; CALCIUM MOBILIZATION; CALCIUM SIGNALING; CALCIUM TRANSPORT; CONTROLLED STUDY; EXCITATION CONTRACTION COUPLING; INTERMEDIATE FILAMENT; MOUSE; MUSCLE CELL; NONHUMAN; PRIORITY JOURNAL; SARCOPLASMIC RETICULUM; SKELETAL MUSCLE;

ACTION POTENTIALS; ANIMALS; DESMIN; INTERMEDIATE FILAMENTS; KERATIN-19; MICE; MICE, INBRED C57BL; MICE, INBRED MDX; MICE, KNOCKOUT; MUSCLE FIBERS, FAST-TWITCH; MUTATION; NEUROMUSCULAR JUNCTION; STRUCTURE-ACTIVITY RELATIONSHIP;

MUS;

EID: 84863902883     PISSN: 03636143     EISSN: 15221563     Source Type: Journal    
DOI: 10.1152/ajpcell.00136.2012     Document Type: Article

References (41)

1. Allen DG. Skeletal muscle function: role of ionic changes in fatigue, damage and disease. Clin Exp Pharmacol Physiol 31: 485-493, 2004.
2. Bloch RJ, Capetanaki Y, O'Neill A, Reed P, Williams MW, Resneck WG, Porter NC, Ursitti JA. Costameres: repeating structures at the sarcolemma of skeletal muscle. Clin Orthop Relat Res S203-S210, 2002.
3. Bloch RJ, Gonzalez-Serratos H. Lateral force transmission across costameres in skeletal muscle. Exerc Sport Sci Rev 31: 73-78, 2003.
4. 2+ sparks and T tubule reorganization in dedifferentiating adult mouse skeletal muscle fibers. Am J Physiol Cell Physiol 292: C1156-C1166, 2007.
5. Brown LD, Schneider MF. Delayed dedifferentiation and retention of properties in dissociated adult skeletal muscle fibers in vitro. In Vitro Cell Dev Biol Anim 38: 411-422, 2002.
6. Canato M, Dal Maschio M, Sbrana F, Raiteri R, Reggiani C, Vassanelli S, Megighian A. Mechanical and electropysiological properties of the sarcolemma of muscle fibers in two murine models of muscle dystrophy: Col6a1+/-and Mdx. J Biomed Biotechnol 2010: 1-13, 2010.
7. Capetanaki Y, Bloch RJ, Kouloumenta A, Mavroidis M, Psarras S. Muscle intermediate filaments and their links to membranes and membranous organelles. Exp Cell Res 313: 2063-2076, 2007.
8. Capote J, Bolanos P, Schuhmeier RP, Melzer W, Caputo C. Calcium transients in developing mouse skeletal muscle fibres. J Physiol 564: 451-464, 2005.
9. Chan S, Head S. The role of branched fibres in the pathogenesis of Duchenne muscular dystrophy. Exp Physiol 96: 564-571, 2011.
10. Chan S, Head SI, Morley JW. Branched fibers in dystrophic mdx muscle are associated with a loss of force following lengthening contractions. Am J Physiol Cell Physiol 293: C985-C992, 2007.
11. Cherednichenko G, Ward CW, Feng W, Cabrales E, Michaelson L, Samso M, Lopez JR, Allen PD, Pessah IN. Enhanced excitation-coupled calcium entry in myotubes expressing malignant hyperthermia mutation R163C is attenuated by dantrolene. Mol Pharmacol 73: 1203-1212, 2008.
12. Collet C, Allard B, Tourneur Y, Jacquemond V. Intracellular calcium signals measured with indo-1 in isolated skeletal muscle fibres from control and mdx mice. J Physiol 520: 417-429, 1999.
13. Coulombe PA, Bousquet O, Ma L, Yamada S, Wirtz D. The 'ins' and 'outs' of intermediate filament organization. Trends Cell Biol 10: 420-428, 2000.
14. Eriksson A, Lindstrom M, Carlsson L, Thornell LE. Hypertrophic muscle fibers with fissures in power-lifters; fiber splitting or defect regeneration? Histochem Cell Biol 126: 409-417, 2006.
15. Friedrich O, Both M, Weber C, Schurmann S, Teichmann M, von Wegner F, Fink R, Vogel M, Chamberlain J, Garbe C. Microarchitecture is severely compromised but motor protein function is preserved in dystrophic mdx skeletal muscle. Biophys J 98: 606-616, 2010.
16. Hayes A, Williams DA. Contractile function and low-intensity exercise effects of old dystrophic (mdx) mice. Am J Physiol Cell Physiol 274: C1138-C1144, 1998.
17. 2+ homeostasis during fatigue. Exp Physiol 95: 641-656, 2010.
18. Head SI, Stephenson DG, Williams DA. Properties of enzymatically isolated skeletal fibres from mice with muscular dystrophy. J Physiol 422: 351-367, 1990.
19. Head SI, Williams DA, Stephenson DG. Abnormalities in structure and function of limb skeletal muscle fibres of dystrophic mdx mice. Proc Biol Sci 248: 163-169, 1992.
20. Hollingworth S, Marshall MW, Robson E. Excitation contraction coupling in normal and mdx mice. Muscle Nerve 13: 16-20, 1990.
21. Hollingworth S, Zeiger U, Baylor SM. Comparison of the myoplasmic calcium transient elicited by an action potential in intact fibres of mdx and normal mice. J Physiol 586: 5063-5075, 2008.
22. Lovering RM, O'Neill A, Muriel JM, Prosser BL, Strong J, Bloch RJ. Physiology, structure, and susceptibility to injurty of skeletal muscle in mice lacking keratin 19-based and desmin-based intermediate filaments. Am J Physiol Cell Physiol 300: C803-C813, 2011.
23. 2+ signaling. Am J Physiol Cell Physiol 297: C571-C580, 2009.
24. Lovering RM, Porter NC, Bloch RJ. The muscular dystrophies: from genes to therapies. Phys Ther 85: 1372-1388, 2005.
25. O'Neill A, Williams MW, Resneck WG, Milner DJ, Capetanaki Y, Bloch RJ. Sarcolemmal organization in skeletal muscle lacking desmin: evidence for cytokeratins associated with the membrane skeleton at costameres. Mol Biol Cell 13: 2347-2359, 2002.
26. Ohlendieck K, Campbell KP. Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice. J Cell Biol 115: 1685-1694, 1991.
27. Ravenscroft G, Nowak KJ, Jackaman C, Clement S, Lyons MA, Gallagher S, Bakker AJ, Laing NG. Dissociated flexor digitorum brevis myofiber culture system-a more mature muscle culture system. Cell Motil Cytoskeleton 64: 727-738, 2007.
28. Robert V, Massimino ML, Tosello V, Marsault R, Cantini M, Sorrentino V, Pozzan T. Alteration in calcium handling at the subcellular level in mdx myotubes. J Biol Chem 276: 4647-4651, 2001.
29. Schertzer JD, van der PC, Shavlakadze T, Grounds MD, Lynch GS. Muscle-specific overexpression of IGF-I improves E-C coupling in skeletal muscle fibers from dystrophic mdx mice. Am J Physiol Cell Physiol 294: C161-C168, 2008.
30. Schmalbruch H. The morphology of regeneration of skeletal muscles in the rat. Tissue Cell 8: 673-692, 1976.
31. Stone MR, O'Neill A, Catino D, Bloch RJ. Specific interaction of the actin-binding domain of dystrophin with intermediate filaments containing keratin 19. Mol Biol Cell 16: 4280-4293, 2005.
32. Stone MR, O'Neill A, Lovering RM, Strong J, Resneck WG, Reed PW, Toivola DM, Ursitti JA, Omary MB, Bloch RJ. Absence of keratin 19 in mice causes skeletal myopathy with mitochondrial and sarcolemmal reorganization. J Cell Sci 120: 3999-4008, 2007.
33. Tamai Y, Ishikawa T, Bosl MR, Mori M, Nozaki M, Baribault H, Oshima RG, Taketo MM. Cytokeratins 8 and 19 in the mouse placental development. J Cell Biol 151: 563-572, 2000.
34. Tamaki T, Sekine T, Akatsuka A, Uchiyama S, Nakano S. Detection of neuromuscular junctions on isolated branched muscle fibers: application of nitric acid fiber digestion method for scanning electron microscopy. J Electron Microsc (Tokyo) 41: 76-81, 1992.
35. Thomas GD, Sander M, Lau KS, Huang PL, Stull JT, Victor RG. Impaired metabolic modulation of alpha-adrenergic vasoconstriction in dystrophin-deficient skeletal muscle. Proc Natl Acad Sci USA 95: 15090-15095, 1998.
36. Ursitti JA, Lee PC, Resneck WG, McNally MM, Bowman AL, O'Neill A, Stone MR, Bloch RJ. Cloning and characterization of cytokeratins 8 and 19 in adult rat striated muscle. Interaction with the dystrophin glycoprotein complex. J Biol Chem 279: 41830-41838, 2004.
37. Ward CW, Reiken S, Marks AR, Marty I, Vassort G, Lacampagne A. Defects in ryanodine receptor calcium release in skeletal muscle from post-myocardial infarct rats. FASEB J 17: 1517-1519, 2003.
38. Willmann R, Possekel S, Dubach-Powell J, Meier T, Ruegg MA. Mammalian animal models for Duchenne muscular dystrophy. Neuromuscul Disord 19: 241-249, 2009.
39. Woods CE, Novo D, DiFranco M, Capote J, Vergara JL. Propagation in the transverse tubular system and voltage dependence of calcium release in normal and mdx mouse muscle fibres. J Physiol 568: 867-880, 2005.
40. Woods CE, Novo D, DiFranco M, Vergara JL. The action potentialevoked sarcoplasmic reticulum calcium release is impaired in mdx mouse muscle fibres. J Physiol 557: 59-75, 2004.
41. i and muscle damage in the mdx mouse. J Physiol 562: 367-380, 2005.