4.7 Article

Super-resolution STED microscopy in live brain tissue

Journal

NEUROBIOLOGY OF DISEASE
Volume 156, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.nbd.2021.105420

Keywords

STED microscopy; Super-resolution; Live imaging; Synapses; Dendritic spines; Brain extracellular space

Categories

Funding

  1. Spanish Ministry of Science and Innovation [SAF201783776R, RYC-2014-15994, IJCI201732114]
  2. Basque Government [PIBA19-0065, PIBA202010061]
  3. University of the Basque Country [GIU18/094, INF1929]

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STED microscopy is a super-resolution technique that allows imaging at higher spatial resolution than the diffraction limit of light, particularly well-suited for imaging inside live brain tissue. Over the past 20 years, STED microscopy has undergone extensive developments and facilitated remarkable neurophysiological discoveries.
STED microscopy is one of several fluorescence microscopy techniques that permit imaging at higher spatial resolution than what the diffraction-limit of light dictates. STED imaging is unique among these super-resolution modalities in being a beam-scanning microscopy technique based on confocal or 2-photon imaging, which provides the advantage of superior optical sectioning in thick samples. Compared to the other super-resolution techniques that are based on widefield microscopy, this makes STED particularly suited for imaging inside live brain tissue, such as in slices or in vivo. Notably, the 50 nm resolution provided by STED microscopy enables analysis of neural morphologies that conventional confocal and 2-photon microscopy approaches cannot resolve, including all-important synaptic structures. Over the course of the last 20 years, STED microscopy has undergone extensive developments towards ever more versatile use, and has facilitated remarkable neurophysiological discoveries. The technique is still not widely adopted for live tissue imaging, even though one of its particular strengths is exactly in resolving the nanoscale dynamics of synaptic structures in brain tissue, as well as in addressing the complex morphologies of glial cells, and revealing the intricate structure of the brain extracellular space. Not least, live tissue STED microscopy has so far hardly been applied in settings of pathophysiology, though also here it shows great promise for providing new insights. This review outlines the technical advantages of STED microscopy for imaging in live brain tissue, and highlights key neurobiological findings brought about by the technique.

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