神经肌肉接头
心肌细胞
缝隙连接
神经科学
连接蛋白
沟道视紫红质
C2C12型
多电极阵列
人口
体外
骨骼肌
光遗传学
生物
细胞生物学
细胞内
化学
微电极
肌发生
解剖
医学
生物化学
物理化学
环境卫生
电极
作者
Emilia Solomon,Allison M. Rooney,Arasely M. Rodriguez,Sofiya Micheva‐Viteva,Rashid Bashir,Rashi Iyer,Jennifer Foster Harris
出处
期刊:Tissue Engineering Part C-methods
[Mary Ann Liebert, Inc.]
日期:2021-02-18
卷期号:27 (4): 242-252
被引量:8
标识
DOI:10.1089/ten.tec.2020.0292
摘要
Neuromuscular junctions (NMJs), specialized synapses between motor neurons and muscle fibers, are essential for muscle activity. A simple and reproducible cell-based in vitro NMJ platform is needed to test the impact of chemicals on the neuron-muscle communication. Our platform utilizes genetically modified neurons and muscle cells, optimized culture conditions, and commercially available multielectrode array system for recording action potentials. Neuronal cells (NSC34) were optogenetically modified with channelrhodopsin chimera to allow for simultaneous, light-mediated, millisecond-precise activation of neuronal population. This signal is propagated through functional synapses to the muscle fibers. Muscle cells (C2C12) were modified by incorporating gap junction protein (Connexin-43) to improve intracellular communication without affecting muscle differentiation. This communication between muscle fibers resulted in better signal propagation and signal strength. Optimized culture medium facilitated the growth and differentiation of both cell types together. Our system was validated using vecuronium, a muscle relaxant, which abolished the muscle response. This in vitro model provides a unique tool for establishing a NMJ platform that is easy to record and analyze. Potential applications include nondestructive long-term screening of drugs affecting the NMJ.
科研通智能强力驱动
Strongly Powered by AbleSci AI