Analysis of embryonic and larval zebrafish skeletal myofibers from dissociated preparations

Journal of Visualized Experiments

Volumn , Issue 81, 2013, Pages

  Horstick, Eric J ^a   Gibbs, Elizabeth M ^a   Li, Xingli ^a   Davidson, Ann E ^a   Dowling, James J ^a  

^a UNIVERSITY OF MICHIGAN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM; DRUG ANALYSIS; MUSCLE PROTEIN;

ANIMAL; ARTICLE; CHEMISTRY; CYTOLOGY; IMMUNOHISTOCHEMISTRY; LARVA; METABOLISM; SKELETAL MUSCLE; ZEBRA FISH;

ANALYSIS; ANIMALS; CALCIUM; CHEMISTRY; CYTOLOGY; IMMUNOHISTOCHEMISTRY; LARVA; METABOLISM; MUSCLE FIBERS, SKELETAL; MUSCLE PROTEINS; MUSCLE, SKELETAL; ZEBRAFISH;

EID: 84995292410     PISSN: 1940087X     EISSN: None     Source Type: Journal    
DOI: 10.3791/50259     Document Type: Article

References (36)

1. Dulhunty, A.F. Excitation-contraction coupling from the 1950s into the new millennium. Clin. Exp. Pharmacol. Physiol. 33, 763-772(2006).
2. Bannister, R.A. Bridging the myoplasmic gap: recent developments in skeletal muscle excitation-contraction coupling. J. Muscle Res. Cell Motil. 28, 275-283(2007).
3. Ohno, K. Genetic defects and disorders at the neuromuscular junction. Brain Nerve. 63, 669-678(2011).
4. Lanner, J.T., Georgiou, D.K., Joshi, A.D., & Hamilton, S.L. Ryanodine receptors: structure, expression, molecular details, and function in calcium release. Cold Spring Harb. Perspect. Biol. 2(2010).
5. Dolphin, A.C. Calcium channel diversity: multiple roles of calcium channel subunits. Curr. Opin. Neurobiol. 19, 237-244(2009).
6. Sparrow, J.C. & Schock, F. The initial steps of myofibril assembly: integrins pave the way. Nat. Rev. Mol. Cell Biol. 10, 293-298(2009).
7. Lapidos, K.A., Kakkar, R., & McNally, E.M. The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma. Circ. Res. 94, 1023-1031(2004).
8. Bassett, D. & Currie, P.D. Identification of a zebrafish model of muscular dystrophy. Clin. Exp. Pharmacol. Physiol. 31, 537-540(2004).
9. Barresi, R. & Campbell, K.P. Dystroglycan: from biosynthesis to pathogenesis of human disease. J. Cell Sci. 119, 199-207(2006).
10. Emery, A.E. Population frequencies of inherited neuromuscular diseases-a world survey. Neuromuscul. Disord. 1, 19-29 (1991).
11. Nance, J.R., Dowling, J.J., Gibbs, E.M., & Bonnemann, C.G. Congenital myopathies: an update. Curr. Neurol. Neurosci. Rep. 12, 165-174(2012).
12. Bassett, D.I. & Currie, P.D. The zebrafish as a model for muscular dystrophy and congenital myopathy. Hum. Mol. Genet. 12 Spec No 2, R265-270(2003).
13. Dooley, K. & Zon, L.I. Zebrafish: a model system for the study of human disease. Curr. Opin. Genet. Dev. 10, 252-256(2000).
14. Dowling, J.J., et al. Loss of myotubularin function results in T-tubule disorganization in zebrafish and human myotubular myopathy. PLoS Genet. 5(2009).
15. Dowling, J.J. et al. Oxidative stress and successful antioxidant treatment in models of RYR1-related myopathy. Brain. 135, 1115-1127(2012).
16. Kawahara, G. et al. Drug screening in a zebrafish model of Duchenne muscular dystrophy. Proc. Natl. Acad. Sci. U.S.A. 108, 5331-5336(2011).
17. Detrich, H.W., 3rd, Westerfield, M. & Zon, L.I. Overview of the Zebrafish system. Methods Cell Biol. 59, 3-10 (1999).
18. Nixon, S.J. et al. Zebrafish as a model for caveolin-associated muscle disease; caveolin-3 is required for myofibril organization and muscle cell patterning. Hum. Mol. Genet. 14, 1727-1743(2005).
19. Schredelseker, J., et al. The beta 1a subunit is essential for the assembly of dihydropyridine-receptor arrays in skeletal muscle. Proc. Natl. Acad. Sci. U.S.A. 102, 17219-17224(2005).
20. Telfer, W.R., Nelson, D.D., Waugh, T., Brooks, S.V., & Dowling, J.J. Neb: a zebrafish model of nemaline myopathy due to nebulin mutation. Dis. Model Mech. 5, 389-396(2012).
21. Dowling, J.J., Low, S.E., Busta, A.S., & Feldman, E.L. Zebrafish MTMR14 is required for excitation-contraction coupling, developmental motor function and the regulation of autophagy. Hum. Mol. Genet. 19, 2668-2681(2010).
22. Schredelseker, J., Dayal, A., Schwerte, T., Franzini-Armstrong, C., & Grabner, M. Proper restoration of excitation-contraction coupling in the dihydropyridine receptor beta1-null zebrafish relaxed is an exclusive function of the beta1a subunit. J. Biol. Chem. 284, 1242-1251(2009).
23. Higashijima, S., Okamoto, H., Ueno, N., Hotta, Y., & Eguchi, G. High-frequency generation of transgenic zebrafish which reliably express GFP in whole muscles or the whole body by using promoters of zebrafish origin. Dev. Biol. 192, 289-299(1997).
24. Tian, L., et al. Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators. Nat. Methods. 6, 875-881(2009).
25. Zhou, W., et al. Non-sense mutations in the dihydropyridine receptor beta1 gene, CACNB1, paralyze zebrafish relaxed mutants. Cell Calcium. 39, 227-236(2006).
26. Dora, K.A., Doyle, M.P., & Duling, B.R. Elevation of intracellular calcium in smooth muscle causes endothelial cell generation of NO in arterioles. Proc. Natl. Acad. Sci. U.S.A. 94, 6529-6534 (1997).
27. Hirata, H., et al. Accordion, a zebrafish behavioral mutant, has a muscle relaxation defect due to a mutation in the ATPase Ca2+ pump SERCA1. Development. 131, 5457-5468(2004).
28. van Eeden, F.J., et al. Mutations affecting somite formation and patterning in the zebrafish, Danio rerio. Development. 123, 153-164 (1996).
29. Gupta, V., et al. The zebrafish dag1 mutant: a novel genetic model for dystroglycanopathies. Hum. Mol. Genet. 20, 1712-1725(2011).
30. Leuranguer, V., Papadopoulos, S., & Beam, K.G. Organization of calcium channel beta1a subunits in triad junctions in skeletal muscle. J. Biol. Chem. 281, 3521-3527(2006).
31. Capote, J., Bolanos, P., Schuhmeier, R.P., Melzer, W., & Caputo, C. Calcium transients in developing mouse skeletal muscle fibres. J. Physiol. 564, 451-464(2005).
32. Adams, B.A., Tanabe, T., Mikami, A., Numa, S., & Beam, K.G. Intramembrane charge movement restored in dysgenic skeletal muscle by injection of dihydropyridine receptor cDNAs. Nature. 346(1990).
33. Sakowski, S.A., et al. A novel approach to study motor neurons from zebrafish embryos and larvae in culture. J. Neurosci. Methods. 205, 277-282(2012).
34. Nakano, Y., et al. Biogenesis of GPI-anchored proteins is essential for surface expression of sodium channels in zebrafish Rohon-Beard neurons to respond to mechanosensory stimulation. Development. 137, 1689-1698(2010).
35. Davidson, A.E., et al. Novel deletion of lysine 7 expands the clinical, histopathological and genetic spectrum of TPM2-related myopathies. Brain. 136, 508-521(2013).
36. Schredelseker, J., Shrivastav, M., Dayal, A., & Grabner, M. Non-Ca2+-conducting Ca2+ channels in fish skeletal muscle excitation-contraction coupling. Proc. Natl. Acad. Sci. U.S.A. 107, 5658-5663(2010).