Expansion-enhanced super-resolution radial fluctuations enable nanoscale molecular profiling of pathology specimens
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Published:2023-04
Issue:4
Volume:18
Page:336-342
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ISSN:1748-3387
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Container-title:Nature Nanotechnology
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language:en
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Short-container-title:Nat. Nanotechnol.
Author:
Kylies Dominik, Zimmermann MarinaORCID, Haas FabianORCID, Schwerk MariaORCID, Kuehl MalteORCID, Brehler Michael, Czogalla Jan, Hernandez Lola C.ORCID, Konczalla LeonieORCID, Okabayashi YusukeORCID, Menzel Julia, Edenhofer Ilka, Mezher Sam, Aypek Hande, Dumoulin Bernhard, Wu HuiORCID, Hofmann Smilla, Kretz Oliver, Wanner Nicola, Tomas Nicola M.ORCID, Krasemann SusanneORCID, Glatzel MarkusORCID, Kuppe ChristophORCID, Kramann RafaelORCID, Banjanin Bella, Schneider Rebekka K., Urbschat ChristopherORCID, Arck PetraORCID, Gagliani Nicola, van Zandvoort Marc, Wiech Thorsten, Grahammer Florian, Sáez Pablo J.ORCID, Wong Milagros N., Bonn StefanORCID, Huber Tobias B.ORCID, Puelles Victor G.ORCID
Abstract
AbstractExpansion microscopy physically enlarges biological specimens to achieve nanoscale resolution using diffraction-limited microscopy systems1. However, optimal performance is usually reached using laser-based systems (for example, confocal microscopy), restricting its broad applicability in clinical pathology, as most centres have access only to light-emitting diode (LED)-based widefield systems. As a possible alternative, a computational method for image resolution enhancement, namely, super-resolution radial fluctuations (SRRF)2,3, has recently been developed. However, this method has not been explored in pathology specimens to date, because on its own, it does not achieve sufficient resolution for routine clinical use. Here, we report expansion-enhanced super-resolution radial fluctuations (ExSRRF), a simple, robust, scalable and accessible workflow that provides a resolution of up to 25 nm using LED-based widefield microscopy. ExSRRF enables molecular profiling of subcellular structures from archival formalin-fixed paraffin-embedded tissues in complex clinical and experimental specimens, including ischaemic, degenerative, neoplastic, genetic and immune-mediated disorders. Furthermore, as examples of its potential application to experimental and clinical pathology, we show that ExSRRF can be used to identify and quantify classical features of endoplasmic reticulum stress in the murine ischaemic kidney and diagnostic ultrastructural features in human kidney biopsies.
Publisher
Springer Science and Business Media LLC
Subject
Electrical and Electronic Engineering,Condensed Matter Physics,General Materials Science,Biomedical Engineering,Atomic and Molecular Physics, and Optics,Bioengineering
Reference45 articles.
1. Wassie, A. T., Zhao, Y. & Boyden, E. S. Expansion microscopy: principles and uses in biological research. Nat. Methods 16, 33–41 (2019). 2. Gustafsson, N. et al. Fast live-cell conventional fluorophore nanoscopy with ImageJ through super-resolution radial fluctuations. Nat. Commun. 7, 12471 (2016). 3. Culley, S. et al. SRRF: universal live-cell super-resolution microscopy. Int. J. Biochem. Cell Biol. 101, 74–79 (2018). 4. Bond, C. et al. Technological advances in super-resolution microscopy to study cellular processes. Mol. Cell 82, 315–332 (2022). 5. Chen, F., Tillberg, P. W. & Boyden, E. S. Expansion microscopy. Science 347, 543–548 (2015).
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