Limitations and Challenges in Modeling Diseases Involving Spinal Motor Neuron Degeneration in Vitro

被引:19
作者
Bucchia, Monica [1 ]
Merwin, Samantha J. [2 ]
Re, Diane B. [2 ]
Kariya, Shingo [1 ]
机构
[1] Columbia Univ, Dept Neurol, Med Ctr, New York, NY 10027 USA
[2] Columbia Univ, Med Ctr, Dept Environm Hlth Sci, New York, NY USA
来源
FRONTIERS IN CELLULAR NEUROSCIENCE | 2018年 / 12卷
关键词
spinal motor neuron; neuromuscular junction; maturation; adult spinal cord; motor neuron culture; amyotrophic lateral sclerosis; sarcopenia; spinal cord injury; VERTEBRATE NEUROMUSCULAR-JUNCTION; PLURIPOTENT STEM-CELLS; CORD SLICE CULTURES; RAT SKELETAL-MUSCLE; NERVE GROWTH-FACTOR; CALCIUM-CHANNELS; SCHWANN-CELLS; NEUROTRANSMITTER RELEASE; SYNAPSE ELIMINATION; NEUROTROPHIC FACTOR;
D O I
10.3389/fncel.2018.00061
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Pathogenic conditions involving degeneration of spinal motor neurons (MNs), such as amyotrophic lateral sclerosis, sarcopenia, and spinal cord injury, mostly occur in individuals whose spinal MNs are fully mature. There is currently no effective treatment to prevent death or promote axonal regeneration of the spinal MNs affected in these patients. To increase our understanding and find a cure for such conditions, easily controllable and monitorable cell culture models allow for a better dissection of certain molecular and cellular events that cannot be teased apart in whole organism models. To date, various types of spinal MN cultures have been described. Yet these models are all based on the use of immature neurons or neurons uncharacterized for their degree of maturity after being isolated and cultured. Additionally, studying only MNs cannot give a comprehensive and complete view of the neurodegenerative processes usually involving other cell types. To date, there is no confirmed in vitro model faithfully emulating disease or injury of the mature spinal MNs. In this review, we summarize the different limitations of currently available culture models, and discuss the challenges that have to be overcome for developing more reliable and translational platforms for the in vitro study of spinal MN degeneration.
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页数:8
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