Normal innervation and differentiation of X-linked myotubular myopathy muscle cells in a nerve-muscle coculture system

Neuromuscular Disorders

Volumn 11, Issue 8, 2001, Pages 736-746

  Dorchies, Olivier M ^a   Laporte, Jocelyn ^b   Wagner, Stéphanie ^a   Hindelang, Colette ^b   Warter, Jean Marie ^a   Mandel, Jean Louis ^b   Poindron, Philippe ^a  

^a UFR de Sciences Pharmaceutiques   (France)

^b INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

Author keywords

In vitro differentiation; Myotubularin; Nerve muscle coculture; X linked myotubular myopathy

Indexed keywords

ALPHA ACTININ; DESMIN; DYSTROPHIN; MONOCLONAL ANTIBODY; MYOSIN HEAVY CHAIN; NICOTINIC RECEPTOR; TROPOMYOSIN; TROPONIN T; VIMENTIN;

ANIMAL TISSUE; ARTICLE; CELL DIFFERENTIATION; CELL FUNCTION; CELL SURVIVAL; CENTRONUCLEAR MYOPATHY; COCULTURE; CONTROLLED STUDY; DISEASE COURSE; EMBRYO; EMBRYONAL TISSUE; EXPLANT; FETUS; GENE MUTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; INNERVATION; MALE; MOTONEURON; MOTOR UNIT; MUSCLE CELL; MUSCLE CONTRACTILITY; NONHUMAN; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; PROTEIN AGGREGATION; PROTEIN EXPRESSION; RAT; SKELETAL MUSCLE; SPINAL CORD; X CHROMOSOME RECESSIVE DISORDER;

ANIMALS; ANTIGENS, DIFFERENTIATION; CELL DIFFERENTIATION; CELL SURVIVAL; CELLS, CULTURED; COCULTURE TECHNIQUES; HUMANS; MALE; MUSCLE CONTRACTION; MUSCLE, SKELETAL; MUTATION; MYOFIBRILS; MYOPATHIES, STRUCTURAL, CONGENITAL; NERVE TISSUE; PHENOTYPE; PROTEIN-TYROSINE-PHOSPHATASE; RATS; RECEPTORS, NICOTINIC; SPINAL CORD; X CHROMOSOME;

EID: 0034804933     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(01)00221-8     Document Type: Article

References (46)

1. The myotubular myopathies: Differential diagnosis of the X-linked recessive, autosomal dominant and autosomal recessive forms and present state of DNA studies
2. Medical complications in long-term survivors with X-linked myotubular myopathy
3. X-linked myotubular myopathy. A long term follow-up study
4. Gene mutated in X-linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast
5. Characterization of the myotubularin tyrosine phosphatase gene family, from yeast to human
6. Association of SET domain and myotubularin-related proteins modulates growth control
7. Myotubularin, a protein tyrosine phosphatase mutated in myotubular myopathy, dephosphorylates the lipid second messenger, phosphatidylinositol 3-phosphate
8. Myotubularin, a phosphatase deficient in myotubular myopathy, acts on phosphatidylinositol 3-kinase and phosphatidylinositol 3-phosphate pathway
9. Congenital myopathies
10. Myotubular myopathy: Morphological, immunohistochemical and clinical variation
11. Myotubular myopathy: Arrest of morphogenesis of myofibres associated with persistence of fetal vimentin and desmin. Four cases compared with fetal and neonatal muscle
12. Centronuclear myopathy heterogeneity: Distinction of clinical types by myosin isoform patterns
13. The role of immunocytochemistry in congenital myopathies
14. Abnormal expression of intermediate filament proteins in X-linked myotubular myopathy is not reproduced in vitro
15. X-linked recessive myotubular myopathy: II. Muscle morphology and human morphogenesis
16. Abberant arrested in maturation neuromuscular junctions in centronuclear myopathy
17. De novo neuromuscular junction formation on human muscle fibres cultured in monolayer and innervated by fœtal rat spinal cord: Ultrastructural and ultrastructural-cytochemical studies
18. Asynchronous regulation of muscle specific isozymes of creatine kinase, glycogen phosphorylase, lactic dehydrogenase and phosphoglycerate mutase in innervated and non-innervated cultured human muscle
19. Different degradation rates of junctional and extrajunctional acetylcholine receptors of human muscle cultured in monolayer and innervated by fetal rat spinal cord neurons
20. Long term treatment with glucocorticoids increases synthesis and stability of junctional acetylcholine receptors on innervated cultured human muscle
21. Abnormalities of aneural and innervated cultured human muscle fibers from patients with myotonic atrophy (dystrophy)
22. Impaired innervation of cultured human muscle overexpressing βAPP experimentally and genetically: Relevance to inclusion-body myopathies
23. Constitutive muscular abnormalities in culture in spinal muscular atrophy
24. Degeneration of cocultures of SMA muscle cells and rat spinal cord explants is not due to secreted factors and cannot be prevented by neurotrophins
25. Muscle could be the therapeutic target in SMA treatment
26. Mutations in the MTM1 gene implicated in X-linked myotubular myopathy
27. Identification of novel mutations in the MTM1 gene causing severe and mild forms of X-linked myotubular myopathy
28. MTM1 mutations in X-linked myotubular myopathy
29. New program for investigating adult human skeletal muscle grown aneurally in tissue culture
30. Synergistic influence of polypeptide growth factors on cultured human musle
31. Human muscle cultured in monolayer and cocultured with fetal spinal cord: Importance of dorsal root ganglia for achieving successful functional innervation
32. Myosin heavy and ligth chain expression during human skeletal muscle development
33. Acetylcholine receptors and acetylcholinesterase accumulate at the nerve-muscle contacts of de novo grown human monolayer muscle cocultured with fetal rat spinal cord
34. The application of organotypic nerve cultures to problems in neurology with special reference to their potential use in research into neuromuscular diseases
35. Myosin heavy chain expression in human muscle cocultured with mouse spinal cord
36. Development of fibre types in human fetal muscle. An immunocytochemical study
37. Myosin heavy and light chain expression during human skeletal muscle development and precocious muscle maturation induced by thyroid hormone
38. Distinct contractile protein profile in congenital myotonic dystrophy and X-linked myotubular myopathy
39. X-linked recessive congenital muscle fibre hypotrophy with central nuclei: Abnormalities of growth and adenylate cyclase in muscle tissue cultures
40. Abnormal distribution of desmin and vimentin in myofibres in adult onset myotubular myopathy
41. Vimentin and desmin in maturing skeletal muscle and developmental myopathies
42. Neurotrophins increase motoneurons' ability to innervate skeletal muscle fibres in rat spinal cord-human muscle cocultures
43. Neonatal myotubular myopathy: Neuropathy and failure of postnatal maturation of fetal muscle
44. Duchenne dystrophic muscle develops lesions in long-term coculture with mouse spinal cord
45. Effects of exposure to low dose pyridostigmine on neuromuscular junctions in vitro
46. Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2