Organ-on-a-chip technologies to study neuromuscular disorders: possibilities, limitations, and future hopes

被引:4
作者
Lauffer, Marten C. [1 ]
机构
[1] Univ Hosp Cologne, Inst Human Genet, Kerpener Str 34, D-50931 Cologne, Germany
关键词
disease modeling; induced pluripotent stem cells; neuromuscular disorders; neuromuscular junction; organ-on-a-chip; GENERATION;
D O I
10.1515/medgen-2021-2085
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Neuromuscular disorders are a heterogeneous group of diseases ranging from mild to devastating phenotypes depending on the disorder's origin. Pathophysiologies for many of these disorders are not fully understood and efficient therapies are urgently needed. Recent advances in the field of induced pluripotent stem cells and organ-on-a-chip technologies have brought enormous improvement in modeling neuromuscular diseases. Even complex units, like the neuromuscular junction, can now be built, enabling researchers to study each component of the motor unit by itself or interacting with others, allowing the identification of disease mechanisms. This article aims to introduce these new modeling systems to study neuromuscular disorders and the possibilities of organ on-a-chip platforms to shed light on disease pathologies and their use for therapy development.
引用
收藏
页码:261 / 267
页数:7
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