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Review
. 2011 Oct;8(4):591-606.
doi: 10.1007/s13311-011-0068-7.

Stem cell transplantation for motor neuron disease: current approaches and future perspectives

Affiliations
Review

Stem cell transplantation for motor neuron disease: current approaches and future perspectives

Genevieve Gowing et al. Neurotherapeutics. 2011 Oct.

Abstract

Motor neuron degeneration leading to muscle atrophy and death is a pathological hallmark of disorders, such as amyotrophic lateral sclerosis or spinal muscular atrophy. No effective treatment is available for these devastating diseases. At present, cell-based therapies targeting motor neuron replacement, support, or as a vehicle for the delivery of neuroprotective molecules are being investigated. Although many challenges and questions remain, the beneficial effects observed following transplantation therapy in animal models of motor neuron disease has sparked hope and a number of clinical trials. Here, we provide a comprehensive review of cell-based therapeutics for motor neuron disorders, with a particular emphasis on amyotrophic lateral sclerosis.

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Figures

Fig. 1
Fig. 1
Schematic representation of possible therapeutic approaches for amyotrophic lateral sclerosis and other motor neuron disorders. CNS = central nervous system; ES embryonic stem cells; iPS = induced pluripotent stem cells; MSCs = mesenchymal stem cells

References

    1. Kanning KC, Kaplan A, Henderson CE. Motor neuron diversity in development and disease. Annual review of neuroscience. 2010;33:409–440. doi: 10.1146/annurev.neuro.051508.135722. - DOI - PubMed
    1. Rothstein JD. Current hypotheses for the underlying biology of amyotrophic lateral sclerosis. Ann Neurol. 2009;65(suppl 1):S3–S9. - PubMed
    1. Saito M, Tomonaga M, Narabayashi H. Histochemical study of the muscle spindles in parkinsonism, motor neuron disease and myasthenia. An examination of the pathological fusimotor endings by the acetylcholinesterase technic. J Neurol. 1978;219:261–271. doi: 10.1007/BF00312979. - DOI - PubMed
    1. Swash M, Fox KP. The pathology of the human muscle spindle: effect of denervation. J Neurol Sci. 1974;22:1–24. doi: 10.1016/0022-510X(74)90050-1. - DOI - PubMed
    1. Swash M, Leader M, Brown A, Swettenham KW. Focal loss of anterior horn cells in the cervical cord in motor neuron disease. Brain. 1986;109(pt 5):939–952. doi: 10.1093/brain/109.5.939. - DOI - PubMed