Skip to main content
Neuroscience Bulletin logoLink to Neuroscience Bulletin
. 2009 Mar 24;25(2):61. doi: 10.1007/s12264-009-0926-2

Permanent myopathy caused by mutation of SCN4A Metl592Val: Observation on myogenesis in vitro and on effect of basic fibroblast growth factor on the muscle

SCN4A Met1592Val突变所致的永久性肌病体外成肌过程观察及碱性成纤维 细胞生长因子的作用

Yu Feng 1, Hong Wang 1, Xiao-Guang Luo 1, Yan Ren 1,
PMCID: PMC5552582  PMID: 19290024

Abstract

Objective

The present study is to observe in vitro the proliferation ability of the muscle cells from permanent myopathy (PM) patients of nomokalaemic periodic paralysis (normKPP), which is caused by mutations of Met1592Val in the skeletal muscle voltage gated sodium channel (SCN4A) gene on chromosome 17q23.1. We also evaluate the possible effect of the foreign basic fibroblast growth factor (bFGF) in preventing and curing PM.

Methods

The gastrocnemius muscle cells were taken from two male patients with PM of the same Chinese family with Met1592Val mutation of SCN4A, determined by gene screening. Four male patients suffering from the skeletal injury without PM were taken as control. All preparations were protogenerationally cultured in vitro. Proliferation of the cultured preparations was measured by MTT. Activities of the lactic dehydrogenase (LDH), creatine kinase (CK), and protein content in these cells were also detected. The effects of bFGF with different doses (10 ng/mL, 20 ng/mL, 40 ng/mL, 80 ng/mL, 120 ng/mL and 160 ng/mL) on the above mentioned parameters were also evaluated.

Results

Cells from both PM and control subjects were successfully cultured in vitro. The cultivation of the muscle cells from PM patients in vitro was not yet seen. Results indicated the obvious stimulation of bFGF on cell proliferation, activities of LDH and CK, protein synthesis, in a dose dependent manner. The optimal dose of bFGF was 120 ng/mL (P<0.05), beyond which greater dose caused a less effect. The effect of bFGF on 160 ng /mL was stronger than that on 80 ng/mL, but there was no significant difference (P>0.05).

Conclusion

Myoblastic cells from patients with PM had a weaker ability of developing into the myotubules, thus they were unable to perform effective regeneration, which resulted in a progressive necrosis. The exogenous bFGF could promote the division and proliferation of the muscle cells in vitro. These results shield a light on bFGF’s potential role in preventing and treating PM.

Key words: SCN4A, permanent myopathy, cell culture, basic fibroblast growth factor

References

  • [1].Kim J., Hahn Y., Sohn E.H., Lee Y.J., Yun J.H., Kim J.M., et al. Phenotypic variation of a Thr704Met mutation in skeletal sodium channel gene in a family with paralysis periodica paramyotonica. J Neurol Neurosurg Psychiatry. 2001;70:618–623. doi: 10.1136/jnnp.70.5.618. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [2].Kelly P., Yang W.S., Costigan D., Farrell M.A., Murphy S., Hardiman O. Paramyotonia congenital and hyperkalemic periodic paralysis associated with a Met1592Val substitution in the skeletal muscle sodium channel alpha subunit-a large kindred with a novel phenotype. Neuromuscular Disord. 1997;7:105–111. doi: 10.1016/S0960-8966(96)00429-4. [DOI] [PubMed] [Google Scholar]
  • [3].Bradley W.G., Taylor R., Rice D.R., Hausmanowa-Petruzewicz I., Adelman L.S., Jenkison M., et al. Progressive myopathy in hyperkalemic periodic paralysis. Arch Neuro. 1990;47:1013–1017. doi: 10.1001/archneur.1990.00530090091018. [DOI] [PubMed] [Google Scholar]
  • [4].MacDonald R.D., Rewcastle N.B., Humphrey J.G. The myopathy of hyperkalemic periodic paralysis an electron microscopic study. Arch Neurol. 1968;19:274–283. doi: 10.1001/archneur.1968.00480030052005. [DOI] [PubMed] [Google Scholar]
  • [5].Feng Y., Wang H., Liu Z.L., Zhang C.D. A paralysis periodica paramytonia family: clinical and molecular genetic studies. Chin J Neurol. 2009;42:152–156. [Google Scholar]
  • [6].Feng Y., Zhang Y., Liu Z.L., Zhang C.D. Exercise test on the patients with normokalaemic periodic paralysis from a Chinese family with amutation in SCN4A gene. Chinese Medical Journal (Egl) 2008;121:1945–1919. [PubMed] [Google Scholar]
  • [7].Carlson B.M., Faulkner J.A. The regeneration of skeletal muscle fiber following injury. Med Sci Sports Exer. 1983;15:187. doi: 10.1249/00005768-198315030-00002. [DOI] [PubMed] [Google Scholar]
  • [8].Chen X.P., Liu H., Wu Y., Liu S.H., Wu H.T. A new method of rapid isolation of adult human myoblast. Chin J Neuromed. 2003;11:404–406. [Google Scholar]
  • [9].Mark M., Martin J. Pinter. Crucial role of sodium channel fast inactivation in muscle fibre inexcitability in a rat model of critical illness myopathy. J Physiol. 2003;547:555–566. doi: 10.1113/jphysiol.2002.035188. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [10].Fishchman D. A. Monoclonal antibodies to desmin:evidence for stage dependent intermediate filament immunoreactivity during cardiac and skeletal muscle development. Ann NY Acad Sci. 1985;455:167. doi: 10.1111/j.1749-6632.1985.tb50411.x. [DOI] [PubMed] [Google Scholar]
  • [11].Lefaucheur J.P., Sebille A. Basic fibroblast growth factor promotes in vivo muscle regeneration in murine muscular dystrophy. Neurosci Lett. 2006;202:121. doi: 10.1016/0304-3940(95)12223-0. [DOI] [PubMed] [Google Scholar]
  • [12].vLiu L., Nicoll C.S. Evidence for a role of basic fibroblast growth factor in rat embryonic growth and differentiation. Endocrinolgy. 1988;123:2027. doi: 10.1210/endo-123-4-2027. [DOI] [PubMed] [Google Scholar]
  • [13].Guthridge M., Wilson M., Cowling J., Bertolini J., Hearn M.T. The role of basic fibroblast growth factors in skeletal muscle regeneration. Growth Factors. 1992;53:161. doi: 10.3109/08977199209008871. [DOI] [PubMed] [Google Scholar]
  • [14].St Clair J.A., Meyer-Demarest S.D., Ham R.G. Improved medium with EGF and BSA for differentiated human skeletal muscle cells. Muscle Nerve. 1992;15:774. doi: 10.1002/mus.880150705. [DOI] [PubMed] [Google Scholar]

Articles from Neuroscience Bulletin are provided here courtesy of Springer

RESOURCES