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iPS cells discover drug target for muscle disease

New induced pluripotent stem cell model reveals calcium ion channels may cause muscle degeneration in muscular dystrophy

Date:
August 20, 2015
Source:
Center for iPS Cell Research and Application - Kyoto University
Summary:
Duchenne muscular dystrophy (DMD) is disease that leads to the degeneration of muscle due to dysfunctional expression of the protein dystrophin. A new iPS cell model found that the early stages of DMD development can be attributed to a specific family of ion channels that allows an abnormal influx of calcium to enter the cell. This same model can be used for drug discovery to correct the channel behavior, experts say.
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Duchenne muscular dystrophy (DMD) is a muscular disease that shows symptoms in early childhood and causes progressive atrophy and eventual death. There is little in terms of treatment, partly because of poor understanding of how DMD develops, although it is known that abnormal expression of the protein dystrophin is at fault. Normally, to study DMD development, patient muscles, the cells that develop into muscle cells, are used to study DMD development. However, because patients suffer from variable stages of DMD, their cells are not suitable for studying the early stages of DMD development and preventative measures. To overcome this problem, Hidetoshi Sakurai, Senior Lecturer at CiRA, and his team, in collaboration with the Institute for Frontier Medical Sciences at Kyoto University, have designed a model that reprograms fibroblasts to the early stages of their differentiation into intact muscle cells.

The strategy depends on first reprogramming the patient cells to induced pluripotent stem (iPS) cells and then introducing a gene that differentiates the iPS cells to muscle cells. "Our model allows us to use the same genetic background to study the early stage of pathogenesis which was not possible in the past," says CiRA researcher Emi Shoji, the first author of a study published in Scientific Reports that gives new insights on DMD development.

Muscle contraction depends on an influx of calcium (Ca2+) ions into the cells. However, too much influx leads to cell dysfunction or death, which is believed to be the underlying cause of DMD. "It is critical to assess intact cells for an accurate evaluation how Ca2+ influx leads to DMD pathogenic cascades," says Shoji. She therefore stimulated their model electrically to simulate muscle cell contraction, finding that cells from DMD patients had significantly increased influx. Further study laid blame on transient receptor potential (TRP) channels through which the Ca2+ ions enter the cell. This observation is consistent with other models and provides a clear drug target for the treatment of DMD. More important, it should allow scientists to uncover drug agents that can counter DMD at early development. "TRP channels have been identified before. But because our model uses patient-derived hiPS cells, there is a potential that we can find new drugs for DMD," says Sakurai.


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Materials provided by Center for iPS Cell Research and Application - Kyoto University. Note: Content may be edited for style and length.


Journal Reference:

  1. Emi Shoji, Hidetoshi Sakurai, Tokiko Nishino, Tatsutoshi Nakahata, Toshio Heike, Tomonari Awaya, Nobuharu Fujii, Yasuko Manabe, Masafumi Matsuo, Atsuko Sehara-Fujisawa. Early pathogenesis of Duchenne muscular dystrophy modelled in patient-derived human induced pluripotent stem cells. Scientific Reports, 2015; 5: 12831 DOI: 10.1038/srep12831

Cite This Page:

Center for iPS Cell Research and Application - Kyoto University. "iPS cells discover drug target for muscle disease." ScienceDaily. ScienceDaily, 20 August 2015. <www.sciencedaily.com/releases/2015/08/150820082506.htm>.
Center for iPS Cell Research and Application - Kyoto University. (2015, August 20). iPS cells discover drug target for muscle disease. ScienceDaily. Retrieved November 5, 2024 from www.sciencedaily.com/releases/2015/08/150820082506.htm
Center for iPS Cell Research and Application - Kyoto University. "iPS cells discover drug target for muscle disease." ScienceDaily. www.sciencedaily.com/releases/2015/08/150820082506.htm (accessed November 5, 2024).

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