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Neuroscience
Optische Klärung und Markierung für die Lichtblatt-Fluoreszenzmikroskopie in der großflächigen Bi...
Optische Klärung und Markierung für die Lichtblatt-Fluoreszenzmikroskopie in der großflächigen Bi...
JoVE Journal
Neuroscience
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JoVE Journal Neuroscience
Optical Clearing and Labeling for Light-sheet Fluorescence Microscopy in Large-scale Human Brain Imaging

Optische Klärung und Markierung für die Lichtblatt-Fluoreszenzmikroskopie in der großflächigen Bildgebung des menschlichen Gehirns

Full Text
2,844 Views
06:52 min
January 26, 2024

DOI: 10.3791/65960-v

Danila Di Meo*1, Josephine Ramazzotti*1, Marina Scardigli*1,2, Franco Cheli1, Luca Pesce1,3, Niamh Brady1, Giacomo Mazzamuto1,4,5, Irene Costantini1,4,6, Francesco S. Pavone1,4,5

1European Laboratory for Non-linear Spectroscopy (LENS),University of Florence, 2Division of Physiology, Department of Experimental and Clinical Medicine,University of Florence, 3Department of Physics,University of Pisa, 4National Research Council - National Institute of Optics (CNR-INO), 5Department of Physics and Astronomy,University of Florence, 6Department of Biology,University of Florence

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Overview

This study presents a high-throughput protocol for simultaneous optical clearing, multi-round labeling, and 3D volumetric reconstruction of postmortem human brain sections. By integrating the S WITCH - H 2 O 2 - Antigen R etrieval - 2,2'-thiodiethanol (TDE) SHORT technique with light-sheet fluorescence microscopy, the methodology allows for detailed structural characterization at micrometer resolution.

Key Study Components

Area of Science

  • Neuroscience
  • Histology
  • Immunohistochemistry

Background

  • The human brain is a complex organ requiring intricate examination across varying scales.
  • Challenges include dealing with large brain samples and autofluorescent signals from pigments.
  • The presented protocol addresses shortcomings of existing clearing techniques.

Purpose of Study

  • To develop a streamlined protocol for analyzing the structure of the human brain.
  • To enhance optical clearing efficiency and imaging quality of brain tissue sections.
  • To enable 3D reconstruction with high detail and reliability.

Methods Used

  • The study employs light-sheet fluorescence microscopy.
  • Human brain tissue is used as a biological model, with detailed sectioning and processing steps outlined.
  • Key steps include embedding samples in agarose, processing with TDE, and multi-round immunostaining for various neuronal markers.
  • Incubation times and temperatures are precisely defined to ensure optimal clearing and imaging conditions.

Main Results

  • The protocol leads to effective optical clearing and high-quality imaging of gray and white matter.
  • Multi-round staining allows visualization of distinct neuronal populations in human brain sections.
  • The method demonstrates the ability to capture subcellular detail in 3D reconstructions.

Conclusions

  • This study establishes a method for comprehensive analysis of brain structure at micrometer resolution.
  • The approach highlights the potential for advancing our understanding of brain architecture and its implications for neuronal studies.

Frequently Asked Questions

What are the advantages of the presented protocol?
The protocol enhances the efficiency of optical clearing and allows for simultaneous multi-round labeling, significantly improving throughput and detail in imaging.
How is the biological model implemented in this study?
The study uses postmortem human brain sections as the biological model, which are subjected to various treatments to ensure optimal imaging and analysis.
What types of data or outcomes are obtained from this method?
The method yields high-resolution 3D reconstructions of brain structure, allowing for detailed cellular and molecular analysis of neuronal populations.
How can the method be applied in other studies?
This protocol can be adapted for various neuronal studies, particularly those exploring brain structure, connectivity, and cellular interactions in health and disease.
Are there any limitations to this protocol?
While the protocol provides high-quality results, it requires careful handling of specimens and precise adherence to incubation times and temperatures to ensure efficacy.

Das vorliegende Protokoll bietet ein Schritt-für-Schritt-Verfahren für die schnelle und gleichzeitige optische Reinigung, die Multi-Round-Markierung und die volumetrische 3D-Rekonstruktion von Dutzenden von postmortalen menschlichen Hirnschnitten durch die Kombination der (SWITCH - H2O2 - Antigen Retrieval - 2,2'-thiodiethanol [TDE]) SHORT-Gewebetransformationstechnik mit Lichtblatt-Fluoreszenzmikroskopie-Bildgebung in einem routinemäßigen Hochdurchsatzprotokoll.

Das menschliche Gehirn ist ein komplexes Organ, das verschiedene Fähigkeiten umfasst. Um seine Funktionsweise zu verstehen, ist es wichtig, eine detaillierte Zellsensorik über das gesamte Gehirn hinweg zu konstruieren. Unser routinemäßiges Hochdurchsatzprotokoll ermöglicht die Analyse der 3D-Zytoarchitektur von volumetrischen Bereichen des menschlichen Gehirns mit Mikrometerauflösung und ermöglicht so die strukturelle Charakterisierung.

Die volumetrische Rekonstruktion großer Bereiche des menschlichen Gehirns stellt mehrere experimentelle Herausforderungen dar, die mit den massiven Abmessungen der Gehirnproben, der komplexen biologischen Zusammensetzung, den variablen postmortalen Fixierungs- und Lagerbedingungen und den autofluoreszierenden Signalen von lipofuszinartigen Pigmenten zusammenhängen. All dies kann die optische Reinigungseffizienz und die Demonstrationsqualität beeinträchtigen. Im Vergleich zu anderen Clearing-Techniken kann die Kurzgewebstransformationsmethode in Kombination mit der Lichtblattmikroskopie für die schnelle und gleichzeitige Verarbeitung mehrerer menschlicher Hirnschnitte verwendet werden.

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