Institute of Pathophysiology, Faculty of Medicine, University of Ljubljana, Zaloška 4, SI-1000 Ljubljana, Slovenia.
Department of Life Sciences, University of Trieste, via A. Fleming 22, I-34127 Trieste, Italy.
Molecules. 2017 Aug 27;22(9):1418. doi: 10.3390/molecules22091418.
Acetylcholinesterase (AChE) and agrin, a heparan-sulfate proteoglycan, reside in the basal lamina of the neuromuscular junction (NMJ) and play key roles in cholinergic transmission and synaptogenesis. Unlike most NMJ components, AChE and agrin are expressed in skeletal muscle and α-motor neurons. AChE and agrin are also expressed in various other types of cells, where they have important alternative functions that are not related to their classical roles in NMJ. In this review, we first focus on co-cultures of embryonic rat spinal cord explants with human skeletal muscle cells as an experimental model to study functional innervation in vitro. We describe how this heterologous rat-human model, which enables experimentation on highly developed contracting human myotubes, offers unique opportunities for AChE and agrin research. We then highlight innovative approaches that were used to address salient questions regarding expression and alternative functions of AChE and agrin in developing human skeletal muscle. Results obtained in co-cultures are compared with those obtained in other models in the context of general advances in the field of AChE and agrin neurobiology.
乙酰胆碱酯酶 (AChE) 和聚集素,一种硫酸乙酰肝素蛋白聚糖,存在于神经肌肉接头 (NMJ) 的基底膜中,在胆碱能传递和突触发生中发挥关键作用。与大多数 NMJ 成分不同,AChE 和聚集素在骨骼肌和 α 运动神经元中表达。AChE 和聚集素也在各种其他类型的细胞中表达,在这些细胞中,它们具有与其在 NMJ 中的经典作用无关的重要替代功能。在这篇综述中,我们首先专注于胚胎大鼠脊髓外植体与人骨骼肌细胞的共培养,作为体外研究功能神经支配的实验模型。我们描述了这种异源大鼠-人类模型如何为 AChE 和聚集素研究提供独特的机会,该模型能够对高度发达的收缩人类肌管进行实验。然后,我们强调了用于解决 AChE 和聚集素在发育中的人类骨骼肌中的表达和替代功能的相关问题的创新方法。在 AChE 和聚集素神经生物学领域的一般进展的背景下,将共培养中获得的结果与其他模型中获得的结果进行了比较。