Helen L. and Martin S. Kimmel Center for Biology and Medicine at the Skirball Institute of Biomolecular Medicine, New York University Medical School, 540 First Avenue, New York, NY 10011, USA.
Departments of Neurology and Human Genetics, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Int J Mol Sci. 2018 Feb 6;19(2):490. doi: 10.3390/ijms19020490.
The neuromuscular synapse is a relatively large synapse with hundreds of active zones in presynaptic motor nerve terminals and more than ten million acetylcholine receptors (AChRs) in the postsynaptic membrane. The enrichment of proteins in presynaptic and postsynaptic membranes ensures a rapid, robust, and reliable synaptic transmission. Over fifty years ago, classic studies of the neuromuscular synapse led to a comprehensive understanding of how a synapse looks and works, but these landmark studies did not reveal the molecular mechanisms responsible for building and maintaining a synapse. During the past two-dozen years, the critical molecular players, responsible for assembling the specialized postsynaptic membrane and regulating nerve terminal differentiation, have begun to be identified and their mechanism of action better understood. Here, we describe and discuss five of these key molecular players, paying heed to their discovery as well as describing their currently understood mechanisms of action. In addition, we discuss the important gaps that remain to better understand how these proteins act to control synaptic differentiation and maintenance.
神经肌肉突触是一个相对较大的突触,在前突触运动神经末梢有数百个活性区,在后突触膜上有超过一千万个乙酰胆碱受体 (AChR)。 突触前膜和突触后膜中蛋白质的丰富度确保了快速、强大和可靠的突触传递。 五十多年前,对神经肌肉突触的经典研究使人们全面了解了突触的外观和工作原理,但这些具有里程碑意义的研究并未揭示负责构建和维持突触的分子机制。 在过去的二十多年中,负责组装特化的突触后膜和调节神经末梢分化的关键分子参与者已开始被识别,并且其作用机制也得到了更好的理解。 在这里,我们描述并讨论了其中的五个关键分子参与者,注意到它们的发现,并描述了它们目前已知的作用机制。 此外,我们还讨论了仍然存在的重要差距,以更好地了解这些蛋白质如何控制突触分化和维持。