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STED Imaging of Vesicular Endocytosis in the Synapse

  • Shaoqin Hu
  • , Zhenli Xie
  • , Bianbian Wang
  • , Yang Chen
  • , Zexin Jing
  • , Ying Hao
  • , Jingyu Yao
  • , Xuanang Wu
  • , Jingxiao Huo
  • , Anqi Wei
  • , Yuhao Qin
  • , Nan Dong
  • , Chaowen Zheng
  • , Qian Song
  • , Jiangang Long
  • , Xinjiang Kang
  • , Changhe Wang
  • , Huadong Xu
  • Xi'an Jiaotong University
  • Southwest Medical University
  • Liaocheng University

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

Endocytosis is a fundamental biological process that couples exocytosis to maintain the homeostasis of the plasma membrane and sustained neurotransmission. Super-resolution microscopy enables optical imaging of exocytosis and endocytosis in live cells and makes an essential contribution to understanding molecular mechanisms of endocytosis in neuronal somata and other types of cells. However, visualization of exo-endocytic events at the single vesicular level in a synapse with optical imaging remains a great challenge to reveal mechanisms governing the synaptic exo-endocytotic coupling. In this protocol, we describe the technical details of stimulated emission depletion (STED) imaging of synaptic endocytosis at the single-vesicle level, from sample preparation and microscopy calibration to data acquisition and analysis.

Original languageEnglish
Pages (from-to)1379-1395
Number of pages17
JournalNeuroscience Bulletin
Volume40
Issue number9
DOIs
StatePublished - Sep 2024

Keywords

  • Endocytosis
  • STED imaging
  • Single-vesicle level
  • Synaptic vesicle

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