Neuromuscular junction‐on‐a‐chip: ALS disease modeling and read‐out development in microfluidic devices
Autor: | Xandor M Spijkers, Rianne de Jongh, R. Jeroen Pasterkamp, Svetlana Pasteuning-Vuhman, Paul Vulto |
---|---|
Rok vydání: | 2021 |
Předmět: |
0301 basic medicine
Cell type Microfluidics Neuromuscular Junction Disease Biology Biochemistry Organ-on-a-chip Neuromuscular junction 03 medical and health sciences Cellular and Molecular Neuroscience 3D cell culture 0302 clinical medicine Lab-On-A-Chip Devices medicine Animals Humans Computer Simulation Amyotrophic lateral sclerosis Induced pluripotent stem cell Motor Neurons Amyotrophic Lateral Sclerosis medicine.disease Phenotype 030104 developmental biology medicine.anatomical_structure nervous system Neuroscience 030217 neurology & neurosurgery |
Zdroj: | Journal of Neurochemistry. 157:393-412 |
ISSN: | 1471-4159 0022-3042 |
DOI: | 10.1111/jnc.15289 |
Popis: | Amyotrophic lateral sclerosis (ALS) is a fatal and progressive neurodegenerative disease affecting upper and lower motor neurons with no cure available. Clinical and animal studies reveal that the neuromuscular junction (NMJ), a synaptic connection between motor neurons and skeletal muscle fibers, is highly vulnerable in ALS and suggest that NMJ defects may occur at the early stages of the disease. However, mechanistic insight into how NMJ dysfunction relates to the onset and progression of ALS is incomplete, which hampers therapy development. This is, in part, caused by a lack of robust in vitro models. The ability to combine microfluidic and induced pluripotent stem cell (iPSC) technologies has opened up new avenues for studying molecular and cellular ALS phenotypes in vitro. Microfluidic devices offer several advantages over traditional culture approaches when modeling the NMJ, such as the spatial separation of different cell types and increased control over the cellular microenvironment. Moreover, they are compatible with 3D cell culture, which enhances NMJ functionality and maturity. Here, we review how microfluidic technology is currently being employed to develop more reliable in vitro NMJ models. To validate and phenotype such models, various morphological and functional read-outs have been developed. We describe and discuss the relevance of these read-outs and specifically illustrate how these read-outs have enhanced our understanding of NMJ pathology in ALS. Finally, we share our view on potential future directions and challenges. |
Databáze: | OpenAIRE |
Externí odkaz: |