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Neuromuscular Disorders
Volume 20, Issue 2
, Pages 111-121
, February 2010
Dexamethasone induces dysferlin in myoblasts and enhances their myogenic differentiation
References
- Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy. Nat Genet. 1998;20:31–36
- A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B. Nat Genet. 1998;20:37–42
- Distal anterior compartment myopathy: a dysferlin mutation causing a new muscular dystrophy phenotype. Ann Neurol. 2001;49:130–134
- . Muscle pathology in dysferlin deficiency. Neuropathol Appl Neurobiol. 2002;28:461–470
- New aspects on patients affected by dysferlin deficient muscular dystrophy. J Neurol Neurosurg Psychiatry. 2009;[Epub ahead of print]
- . Inflammation in dysferlin myopathy: immunohistochemical characterization of 13 patients. Neurology. 2001;57:2136–2138
- . Clarifying the boundaries between the inflammatory and dystrophic myopathies: insights from molecular diagnostics and microarrays. Rheum Dis Clin North Am. 2002;28:743–757
- Muscle inflammation and MHC class I up-regulation in muscular dystrophy with lack of dysferlin: an immunopathological study. J Neuroimmunol. 2003;142:130–136
- Clinical, morphological and immunological evaluation of six patients with dysferlin deficiency. Acta Neuropathol (Berl). 2003;105:537–542
- . Muscle inflammation, autoimmune Addison’s disease and sarcoidosis in a patient with dysferlin deficiency. Neuromuscul Disord. 2006;16:208–209
- Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypes. Arch Neurol. 2007;64:1176–1182
- A new phenotype of dysferlinopathy with congenital onset. Neuromuscul Disord. 2009;19:21–25
- Dysferlin is a plasma membrane protein and is expressed early in human development. Hum Mol Genet. 1999;8:855–861[Erratum in: Hum Mol Genet 1999;8:1141]
- The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle. Hum Mol Genet. 2001;10:1761–1766
- Defective membrane repair in dysferlin-deficient muscular dystrophy. Nature. 2003;423:168–172
- . Dysferlin interacts with annexins A1 and A2 and mediates sarcolemmal wound-healing. J Biol Chem. 2003;278:50466–50473
- Absence of dysferlin alters myogenin expression and delays human muscle differentiation “in vitro”. J Biol Chem. 2006;281:17092–17098
- . Dysferlin in membrane trafficking and patch repair. Traffic. 2007;8:785–794
- Normal myoblast fusion requires myoferlin. Development. 2005;132:5565–5575
- From T-tubule to sarcolemma: damage-induced dysferlin translocation in early myogenesis. FASEB J. 2007;21:1768–1776
- Attenuated muscle regeneration is a key factor in dysferlin deficient muscular dystrophy. Hum Mol Genet. 2009;18:1976–1989
- . Glucocorticoid corticosteroids for Duchenne muscular dystrophy. Cochrane Database Syst Rev. 2008;1:CD003725
- . The role of corticosteroids in muscular dystrophy: a critical appraisal. Muscle Nerve. 2007;36:424–435
- . Deflazacort increases laminin expression and myogenic repair, and induces early persistent functional gain in mdx mouse muscular dystrophy. Cell Transplant. 2000;9:551–564
- . Strength and corticosteroid responsiveness of mdx mice is unchanged by RAG2 gene knockout. Neuromuscul Disord. 2007;17:376–384
- Target-specific utilization of transcriptional regulatory surfaces by the glucocorticoid receptor. Proc Natl Acad Sci USA. 2003;100:13845–13850
- . Crosstalk pathway for inhibition of glucocorticoid-induced apoptosis by T cell receptor signaling. Proc Natl Acad Sci USA. 2000;97:7319–7324
- Structure and specificity of nuclear receptor-coactivator interactions. Genes Dev. 1998;12:3343–3356
- Skeletal muscle: a dual system to measure glucocorticoid-dependent transactivation and transrepression of gene regulation. J Steroid Biochem Mol Biol. 2004;88:191–201
- . Plasticity of human skeletal muscle: gene expression to in vivo function. Exp Physiol. 2007;92:783–797
- . Glucocorticoid inhibition of C2C12 proliferation rate and differentiation capacity in relation to mRNA levels of the MRF gene family. Mol Biol Rep. 2000;27:87–98
- . Glucocorticoids differentially regulate degradation of MyoD and Id1 by N-terminal ubiquitination to promote muscle protein catabolism. Proc Natl Acad Sci USA. 2008;105:3339–3344
- Skeletal muscle hypertrophy is mediated by a Ca2+-dependent calcineurin signalling pathway. Nature. 1999;400:576–581
- . Quantification of hormone-induced atrophy of large myotubes from C2C12 and L6 cells: atrophy-inducible and atrophy-resistant C2C12 myotubes. Am J Physiol Cell Physiol. 2006;290:C650–C659
- Maxwell MM, Brown RH, manuscript in preparation.
- . Notch signaling imposes two distinct blocks in the differentiation of C2C12 myoblasts. Development. 1999;126:1689–1702
- . Stem cell plasticity revisited: CXCR4-positive cells expressing mRNA for early muscle, liver and neural cells ‘hide out’ in the bone marrow. Leukemia. 2004;18:29–40
- . PGC-1alpha is induced by parathyroid hormone and coactivates Nurr1-mediated promoter activity in osteoblasts. Bone. 2006;39:1018–1025
- . Quantitative evaluation and selection of reference genes in mouse oocytes and embryos cultured in vivo and in vitro. BMC Dev Biol. 2007;7:14
- Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol. 2002;3:RESEARCH0034.1-0034.12
- . Analyzing real-time PCR data by the comparative C(T) method. Nat Protoc. 2008;3:1101–1108
- . Analysis of relative gene expression data using real-time quantitative PCR and the 2(−Delta Delta C(T)) method. Methods. 2001;25:402–408
- . Chronic treatment with agents that stabilize cytosolic IkappaB-alpha enhances survival and improves resting membrane potential in MDX muscle fibers subjected to chronic passive stretch. Neurobiol Dis. 2005;20:719–730
- A deletion at the mouse Xist gene exposes trans-effects that alter the heterochromatin of the inactive X chromosome and the replication time and DNA stability of both X chromosomes. Genetics. 2006;174:1115–1133
- . IRES-mediated translation of utrophin A is enhanced by glucocorticoid treatment in skeletal muscle cells. PLoS ONE. 2008;3:e2309
- The third human FER-1-like protein is highly similar to dysferlin. Genomics. 2000;68:313–321
- . Prednisolone-induced changes in dystrophic skeletal muscle. FASEB J. 2005;19:834–836Erratum in: FASEB J 2005 May;19(7):1 p following 836. Hoffmann, Eric P [corrected to Hoffman, Eric P]
- Relationships between circadian rhythms and modulation of gene expression by glucocorticoids in skeletal muscle. Am J Physiol Regul Integr Comp Physiol. 2008;295:R1031–R1047
- Myogenic Akt signaling upregulates the utrophin–glycoprotein complex and promotes sarcolemma stability in muscular dystrophy. Hum Mol Genet. 2009;18:318–327
- Expression of myoferlin in skeletal muscles of patients with dysferlinopathy. Tohoku J Exp Med. 2006;209:109–116
- . A temporal switch from notch to Wnt signaling in muscle stem cells is necessary for normal adult myogenesis. Cell Stem Cell. 2008;2:50–59
- Limb-girdle muscular dystrophy: diagnostic evaluation, frequency and clues to pathogenesis. Neuromuscul Disord. 2008;18:34–44
- . Regulation of the M-cadherin-beta-catenin complex by calpain 3 during terminal stages of myogenic differentiation. Mol Cell Biol. 2006;26:8437–8447
- . Characterisation of the dysferlin skeletal muscle promoter. Eur J Hum Genet. 2004;12:127–131
- Cooperative synergy between NFAT and MyoD regulates myogenin expression and myogenesis. J Biol Chem. 2008;283:29004–29010
- Belanto JJ, Jamieson CAM, manuscript in preparation.
- . Combinatorial role for NFAT5 in both myoblast migration and differentiation during skeletal muscle myogenesis. J Cell Sci. 2007;120:149–159
- . Identification of novel pathway regulation during myogenic differentiation. Genomics. 2006;87:129–138
- Genetic disruption of calcineurin improves skeletal muscle pathology and cardiac disease in a mouse model of limb-girdle muscular dystrophy. J Biol Chem. 2007;282:10068–10078
- Highly efficient, functional engraftment of skeletal muscle stem cells in dystrophic muscles. Cell. 2008;134:37–47
PII: S0960-8966(09)00700-7
doi: 10.1016/j.nmd.2009.12.003
© 2009 Elsevier B.V. All rights reserved.
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Neuromuscular Disorders
Volume 20, Issue 2
, Pages 111-121
, February 2010
