Expression of chloride channel 1 mRNA in cultured myogenic cells: A marker of myotube maturation

Bardouille C, Vullhorst D, Jockusch H (1996)
FEBS letters 396(2-3): 177-180.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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Autor*in
Bardouille, C; Vullhorst, D; Jockusch, HaraldUniBi
Abstract / Bemerkung
The chloride channel ClC-1 is required to maintain a normal excitability of mature muscle fibers; its blockade leads to hyperexcitability, the hallmark of the disease myotonia. In mouse and rat myotubes, representing the embryonic stage of muscle, ClC-1 mRNA is not detectable by Northern blotting. From neonatal to adult, ClC-1 expression increases at least fourfold. Using RT-PCR and hybridization on cultured myotubes we found ClC-1 mRNA at a level of 0.4-1.1% of that in mature mouse muscle, and less than or equal to 0.01% in myoblasts, at stages when desmin mRNA levels are already high. The level of ClC-1 mRNA is thus a sensitive and specific indicator of the maturation of skeletal muscle cells.
Stichworte
quantitative RT-PCR; skeletal muscle development; cell culture; chloride channel 1; myotonia
Erscheinungsjahr
1996
Zeitschriftentitel
FEBS letters
Band
396
Ausgabe
2-3
Seite(n)
177-180
ISSN
0014-5793
Page URI
https://pub.uni-bielefeld.de/record/1638132

Zitieren

Bardouille C, Vullhorst D, Jockusch H. Expression of chloride channel 1 mRNA in cultured myogenic cells: A marker of myotube maturation. FEBS letters. 1996;396(2-3):177-180.
Bardouille, C., Vullhorst, D., & Jockusch, H. (1996). Expression of chloride channel 1 mRNA in cultured myogenic cells: A marker of myotube maturation. FEBS letters, 396(2-3), 177-180. https://doi.org/10.1016/0014-5793(96)01098-8
Bardouille, C, Vullhorst, D, and Jockusch, Harald. 1996. “Expression of chloride channel 1 mRNA in cultured myogenic cells: A marker of myotube maturation”. FEBS letters 396 (2-3): 177-180.
Bardouille, C., Vullhorst, D., and Jockusch, H. (1996). Expression of chloride channel 1 mRNA in cultured myogenic cells: A marker of myotube maturation. FEBS letters 396, 177-180.
Bardouille, C., Vullhorst, D., & Jockusch, H., 1996. Expression of chloride channel 1 mRNA in cultured myogenic cells: A marker of myotube maturation. FEBS letters, 396(2-3), p 177-180.
C. Bardouille, D. Vullhorst, and H. Jockusch, “Expression of chloride channel 1 mRNA in cultured myogenic cells: A marker of myotube maturation”, FEBS letters, vol. 396, 1996, pp. 177-180.
Bardouille, C., Vullhorst, D., Jockusch, H.: Expression of chloride channel 1 mRNA in cultured myogenic cells: A marker of myotube maturation. FEBS letters. 396, 177-180 (1996).
Bardouille, C, Vullhorst, D, and Jockusch, Harald. “Expression of chloride channel 1 mRNA in cultured myogenic cells: A marker of myotube maturation”. FEBS letters 396.2-3 (1996): 177-180.

10 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

HTS-Compatible Patient-Derived Cell-Based Assay to Identify Small Molecule Modulators of Aberrant Splicing in Myotonic Dystrophy Type 1.
O'Leary DA, Vargas L, Sharif O, Garcia ME, Sigal YJ, Chow SK, Schmedt C, Caldwell JS, Brinker A, Engels IH., Curr Chem Genomics 4(), 2010
PMID: 20502647
Chloride channelopathy in myotonic dystrophy resulting from loss of posttranscriptional regulation for CLCN1.
Lueck JD, Lungu C, Mankodi A, Osborne RJ, Welle SL, Dirksen RT, Thornton CA., Am J Physiol Cell Physiol 292(4), 2007
PMID: 17135300
Muscle chloride channel dysfunction in two mouse models of myotonic dystrophy.
Lueck JD, Mankodi A, Swanson MS, Thornton CA, Dirksen RT., J Gen Physiol 129(1), 2007
PMID: 17158949
Misregulation of alternative splicing causes pathogenesis in myotonic dystrophy.
Kuyumcu-Martinez NM, Cooper TA., Prog Mol Subcell Biol 44(), 2006
PMID: 17076268
Molecular structure and physiological function of chloride channels.
Jentsch TJ, Stein V, Weinreich F, Zdebik AA., Physiol Rev 82(2), 2002
PMID: 11917096
Mdx myotubes have normal excitability but show reduced contraction-relaxation dynamics.
Nicolas-Metral V, Raddatz E, Kucera P, Ruegg UT., J Muscle Res Cell Motil 22(1), 2001
PMID: 11563551
Chloride conductance in mouse muscle is subject to post-transcriptional compensation of the functional Cl- channel 1 gene dosage.
Chen MF, Niggeweg R, Iaizzo PA, Lehmann-Horn F, Jockusch H., J Physiol 504 ( Pt 1)(), 1997
PMID: 9350619

27 References

Daten bereitgestellt von Europe PubMed Central.

Development of electrical myotonia in the ADR mouse: role of chloride conductance in myotubes and neonatal animals.
Wischmeyer E, Nolte E, Klocke R, Jockusch H, Brinkmeier H., Neuromuscul. Disord. 3(4), 1993
PMID: 8268723
Membrane ionic conductances in normal and denervated skeletal muscle of the rat during development.
Conte Camerino D, De Luca A, Mambrini M, Vrbova G., Pflugers Arch. 413(5), 1989
PMID: 2740209
Membrane changes in cells from myotonia patients.
Rudel R, Lehmann-Horn F., Physiol. Rev. 65(2), 1985
PMID: 2580324

AUTHOR UNKNOWN, 0
The myotonic mouse mutant ADR: electrophysiology of the muscle fiber.
Mehrke G, Brinkmeier H, Jockusch H., Muscle Nerve 11(5), 1988
PMID: 2453798
Inactivation of muscle chloride channel by transposon insertion in myotonic mice.
Steinmeyer K, Klocke R, Ortland C, Gronemeier M, Jockusch H, Grunder S, Jentsch TJ., Nature 354(6351), 1991
PMID: 1659665

AUTHOR UNKNOWN, 0

Bardouille, Eur. J. Cell Biol. (Suppl.) (), 1995

AUTHOR UNKNOWN, 0

AUTHOR UNKNOWN, 0

AUTHOR UNKNOWN, 0

AUTHOR UNKNOWN, 0
Inhibition of desmin expression blocks myoblast fusion and interferes with the myogenic regulators MyoD and myogenin.
Li H, Choudhary SK, Milner DJ, Munir MI, Kuisk IR, Capetanaki Y., J. Cell Biol. 124(5), 1994
PMID: 8120103
Nonsense and missense mutations in the muscular chloride channel gene Clc-1 of myotonic mice.
Gronemeier M, Condie A, Prosser J, Steinmeyer K, Jentsch TJ, Jockusch H., J. Biol. Chem. 269(8), 1994
PMID: 8119941

Kawasaki, Amplifications 3(), 1989
Neural regulation of parvalbumin expression in mammalian skeletal muscle.
Leberer E, Pette D., Biochem. J. 235(1), 1986
PMID: 3741391
Exploring the mammalian neuromuscular system by analysis of mutations: spinal muscular atrophy and myotonia.
Jockusch H, Kaupmann K, Gronemeier M, Schleef M, Klocke R., Prog. Neurobiol. 42(2), 1994
PMID: 8008830

AUTHOR UNKNOWN, 0
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