» Articles » PMID: 36351828

Super-Resolution Microscopy Opens New Doors to Life at the Nanoscale

Overview
Journal J Neurosci
Specialty Neurology
Date 2022 Nov 9
PMID 36351828
Authors
Affiliations
Soon will be listed here.
Abstract

Super-resolution fluorescence microscopy holds tremendous potential for discovery in neuroscience. Much of the molecular machinery and anatomic specializations that give rise to the unique and bewildering electrochemical activity of neurons are nanoscale by design, ranging somewhere between 1 nm and 1 μm. It is at this scale where most of the unknown and exciting action is and where cell biologists flock to in their dreams, but it was off limits for light microscopy until recently. While the optical principles of super-resolution microscopy are firmly established by now, the technology continues to advance rapidly in many crucial areas, enhancing its performance and reliability, and making it more accessible and user-friendly, which is sorely needed. Indeed, super-resolution microscopy techniques are nowadays widely used for visualizing immunolabeled protein distributions in fixed or living cells. However, a great potential of super-resolution microscopy for neuroscience lies in shining light on the nanoscale structures and biochemical activities in live-tissue settings, which should be developed and harnessed much more fully. In this review, we will present several vivid examples based on STED and RESOLFT super-resolution microscopy, illustrating the possibilities and challenges of nano-imaging to pique the interest of tech-developers and neurobiologists alike. We will cover recent technical progress that is facilitating applications, and share new biological insights into the nanoscale mechanisms of cellular communication between neurons and glia.

Citing Articles

Live STED imaging of functional neuroanatomy.

Arizono M, Idziak A, Nagerl U Nat Protoc. 2025; .

PMID: 40087378 DOI: 10.1038/s41596-024-01132-6.


Bellymount-pulsed tracking: a novel approach for real-time in vivo imaging of Drosophila abdominal tissues.

Balachandra S, Amodeo A G3 (Bethesda). 2024; 15(1.

PMID: 39556480 PMC: 11708215. DOI: 10.1093/g3journal/jkae271.


Super-resolution microscopy to study membrane nanodomains and transport mechanisms in the plasma membrane.

Zulueta Diaz Y, Arnspang E Front Mol Biosci. 2024; 11:1455153.

PMID: 39290992 PMC: 11405310. DOI: 10.3389/fmolb.2024.1455153.


Progress in Structural and Functional In Vivo Imaging of Microglia and Their Application in Health and Disease.

Crockett A, Fuhrmann M, Garaschuk O, Davalos D Adv Neurobiol. 2024; 37:65-80.

PMID: 39207687 DOI: 10.1007/978-3-031-55529-9_5.


Editorial: 15 years of Frontiers in Cellular Neuroscience: super-resolution microscopy in the healthy and the injured brain.

Dzyubenko E, Chen J, Willig K Front Cell Neurosci. 2024; 18:1448206.

PMID: 39045534 PMC: 11263278. DOI: 10.3389/fncel.2024.1448206.


References
1.
Tonnesen J, Inavalli V, Nagerl U . Super-Resolution Imaging of the Extracellular Space in Living Brain Tissue. Cell. 2018; 172(5):1108-1121.e15. DOI: 10.1016/j.cell.2018.02.007. View

2.
Engert F, Bonhoeffer T . Dendritic spine changes associated with hippocampal long-term synaptic plasticity. Nature. 1999; 399(6731):66-70. DOI: 10.1038/19978. View

3.
Arizono M, Inavalli V, Panatier A, Pfeiffer T, Angibaud J, Levet F . Structural basis of astrocytic Ca signals at tripartite synapses. Nat Commun. 2020; 11(1):1906. PMC: 7170846. DOI: 10.1038/s41467-020-15648-4. View

4.
Steffens H, Mott A, Li S, Wegner W, Svehla P, Kan V . Stable but not rigid: Chronic in vivo STED nanoscopy reveals extensive remodeling of spines, indicating multiple drivers of plasticity. Sci Adv. 2021; 7(24). PMC: 8189587. DOI: 10.1126/sciadv.abf2806. View

5.
Steffens H, Wegner W, Willig K . In vivo STED microscopy: A roadmap to nanoscale imaging in the living mouse. Methods. 2019; 174:42-48. DOI: 10.1016/j.ymeth.2019.05.020. View