Optical Approaches to Dissect the Structure and Dynamics of the Synapse at Nanoscale Resolution.

Q3 Neuroscience
Jongyun Myeong, Vitaly A Klyachko
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引用次数: 0

Abstract

The complex nanostructure and spatiotemporal dynamics of central synapses remain among the fundamental mysteries of neurobiology. The resolution of traditional microscopy techniques-constrained by the intrinsic limits of light diffraction-is largely insufficient to study central synapses effectively. Conventional imaging can resolve areas roughly the size of a synapse's active zone, that is, severalfold larger than the size of synaptic vesicles. Recent advances have generated several super-resolution imaging modalities that overcome or bypass the light diffraction limit to support studies of synaptic nanostructure. In this chapter, we present the principles, features, and limitations of the most common super-resolution imaging tools. Though these advancements have greatly improved our understanding of synaptic architecture and dynamics, significant challenges remain. Difficulties of translating the existing tools to in vivo applications, and the inherent trade-off between spatial and temporal resolution, continue to limit studies of the function of central synapses in native tissue.

在纳米尺度分辨率下解剖突触结构和动力学的光学方法。
中枢突触的复杂纳米结构和时空动力学仍然是神经生物学的基本奥秘之一。传统显微镜技术的分辨率受限于光衍射的固有限制,在很大程度上不足以有效地研究中枢突触。传统成像技术可以分辨出突触活跃区大小的区域,也就是说,比突触囊泡大小大几倍。最近的进展产生了几种克服或绕过光衍射极限的超分辨率成像模式,以支持突触纳米结构的研究。在本章中,我们介绍了最常见的超分辨率成像工具的原理、特点和局限性。虽然这些进步大大提高了我们对突触结构和动力学的理解,但仍然存在重大挑战。将现有工具转化为体内应用的困难,以及空间和时间分辨率之间固有的权衡,继续限制了对天然组织中中枢突触功能的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advances in neurobiology
Advances in neurobiology Neuroscience-Neurology
CiteScore
2.80
自引率
0.00%
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