Dynamic restoration of dystrophin to dystrophin-deficient myotubes

Muscle and Nerve

Volumn 24, Issue 1, 2001, Pages 77-88

  Kong, Jiming ^a   Anderson, Judy E ^a  

^a UNIVERSITY OF MANITOBA   (Canada)

Author keywords

Diffusion; Domain; Duchenne muscular dystrophy; Dystrophin; mdx mouse; Myoblast transplantation

Indexed keywords

CHOLINERGIC RECEPTOR; DYSTROPHIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL DIFFERENTIATION; CONTROLLED STUDY; DIFFUSION; DUCHENNE MUSCULAR DYSTROPHY; HYBRID CELL; IMMUNOFLUORESCENCE TEST; IMMUNOHISTOCHEMISTRY; MOUSE; MYOTUBE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN EXPRESSION; PROTEIN STRUCTURE; SATELLITE CELL;

ANIMALS; CELL COUNT; CELL DIFFERENTIATION; CELL DIVISION; CELLS, CULTURED; COCULTURE TECHNIQUES; CYTOSKELETAL PROTEINS; DYSTROGLYCANS; DYSTROPHIN; HYBRID CELLS; MEMBRANE GLYCOPROTEINS; MICE; MICE, INBRED C57BL; MICE, INBRED MDX; MUSCLE PROTEINS; MUSCLE, SKELETAL; MUSCULAR DYSTROPHY, ANIMAL; RECEPTOR PROTEIN-TYROSINE KINASES; RECEPTORS, CHOLINERGIC;

EID: 0035168122     PISSN: 0148639X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1097-4598(200101)24:1<77::AID-MUS9>3.0.CO;2-Q     Document Type: Article

References (57)

1. Skeletal muscle satellite cell cultures
2. Studies of the dynamics of skeletal muscle regeneration: The mouse came back!
3. Functional regeneration in the hindlimb skeletal muscle of the mdx mouse
4. Dystrophy and myogenesis in mdx diaphragm muscle
5. Dynamics of myoblast transplantation reveal a discrete minority of precursors with stern cell-like properties as the myogenic source
6. Histopathological changes in Duchenne muscular dystrophy
7. Spatial relationships of utrophin, dystrophin, beta-dystroglycan and beta-spectrin to acetylcholine receptor clusters during postnatal maturation of the rat neuromuscular junction
8. Dystrophic phenotype induced in vitro by antibody blockade of muscle alpha-dystroglycanlaminin interaction
9. Acetylcholine receptor and calcium leakage activity in nondystrophic and dystrophic myotubes (MDX)
10. The dystrophinopathies: An alternative to the structural hypothesis
11. Segmental necrosis and its demarcation in experimental micropuncture injury of skeletal muscle fibers
12. Interactions between dystrophin and the sarcolemma membrane
13. Expression and subcellular localization of dystrophin in skeletal, cardiac and smooth muscles during the human development
14. A statistical analysis of the loss of muscle strength in Duchenne's muscular dystrophy
15. Signals mediating ion channel clustering at the neuromuscular junction
16. Dystrophin-associated protein abnormalities in dystrophin-deficient muscle fibers from symptomatic and asymptomatic Duchenne/Becker muscular dystrophy carriers
17. Primary, secondary and tertiary myotubes in developing skeletal muscle: A new approach to the analysis of human myogenesis
18. Spatial distribution of beta-spectrin in normal and dystrophic human skeletal muscle
19. Increased activity of calcium leak channels in myotubes of Duchenne human and mdx mouse origin
20. The fate of individual myoblasts after transplantation into muscles of DMD patients
21. Dystroglycan: An extracellular matrix receptor linked to the cytoskeleton
22. A role for dystroglycan in basement membrane assembly
23. Dystrophin expression in myotubes formed by the fusion of normal and dystrophic myoblasts
24. Characterization of delta-sarcoglycan, a novel component of the oligomeric sarcoglycan complex involved in limb-girdle muscular dystrophy
25. Identification and characterization of the dystrophin anchoring site on beta-dystroglycan
26. Molecular therapy for genetic muscle diseases - Status 1999
27. Dystrophin is expressed in mdx skeletal muscle fibers after normal myoblast implantation
28. Transplantation of myoblasts from a transgenic mouse overexpressing dystrophin prduced only a relatively small increase of dystrophin-positive membrane
29. Dystrophin is required for organizing large acetylcholine receptor aggregates
30. Dystrophin as a focal adhesion protein colocalization with talin and the Mr 4800 sarcolemmal protein in cultured Xenopus muscle
31. Sodium current and membrane potential in EDL muscle fibers from normal and dystrophic mdx mice
32. Slow and fast myosin heavy chain content defines three types of myotubes in early muscle cell cultures
33. Myoblast implantation in Duchenne muscular dystrophy: The San Francisco study
34. Immunocytochemical study of dystrophin in muscle cultures from patients with Duchenne muscular dystrophy and unaffected control patients
35. Dystrophin: Localization and presumed function
36. alpha-Dystroglycan is a laminin receptor involved in extracellular matrix assembly on myotubes and muscle cell viability
37. Satellite cell mitotic activity in posthatch turkey skeletal muscle growth
38. Monoclonal antibody evidence for structural similarities between the central rod regions of actinin and dystrophin
39. Dystrophin-associated proteins are greatly reduced in skeletal muscle from mdx mice
40. Is myoblast transplantation effective?
41. Hyperthyroidism impairs early repair in normal but not dystrophic mdx mouse tibialis anterior muscle. An in vivo study
42. Does utrophin expression in muscles of mdx mice during postnatal development functionally compensate for dystrophin deficiency?
43. Forced expression of dystrophin deletion constructs reveals structure-function correlations
44. A new model for the interaction of dystrophin with F-actin
45. Immunostaining of dystrophin and utrophin in skeletal muscle of dystrophinopathies
46. Regenerated muscle fibers in Duchenne muscular dystrophy: A serial section study
47. Is dystrophin labeling always discontinuous in Becker muscular dystrophy?
48. Muscular dystrophics and the dystrophin-glycoprotein complex
49. Characterization of revertant muscle fibers in Duchenne muscular dystrophy, using exon-specific monoclonal antibodies against dystrophin
50. Increased calcium entry into dystrophin-deficient muscle fibres of MDX and ADR-MDX mice is reduced by ion channel blockers
51. Further evidence for the organisation of the four sarcoglycans proteins within the dystrophin-glycoprotein complex
52. Dystrophin distribution in heterozygote mdx mice
53. Dystrophin: A clinical perspective
54. Extensive but coordinated reorganization of the membrane skeleton in myofibers of dystrophic (mdx) mice
55. Revertant fibres: A possible genetic therapy for Duchenne muscular dystrophy?
56. Acetylcholine receptors in innervated muscles of dystrophic mdx mice degrade as after denervation
57. Identification of alpha-syntrophin binding to syntrophin triplet, dystrophin, and utrophin