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Neuroscience
Pulizia ottica ed etichettatura per la microscopia a fluorescenza a foglio luminoso nell'imaging ...
Pulizia ottica ed etichettatura per la microscopia a fluorescenza a foglio luminoso nell'imaging ...
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

Pulizia ottica ed etichettatura per la microscopia a fluorescenza a foglio luminoso nell'imaging cerebrale umano su larga scala

Full Text
2,856 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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Please note that some of the translations on this page are AI generated. Click here for the English version.

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.

Il presente protocollo fornisce una procedura passo-passo per la clearing ottica rapida e simultanea, la marcatura multi-round e la ricostruzione volumetrica 3D di decine di sezioni di cervello umano post-mortem combinando la tecnica di trasformazione tissutale corta (SWITCH - H2O2 - Antigen Retrieval - 2,2'-tiodiethanol [TDE]) SHORT con l'imaging al microscopio a fluorescenza a foglio luminoso in un protocollo di routine ad alto rendimento.

Il cervello umano è un organo complesso che abbraccia diverse abilità. Per comprenderne la funzionalità, è essenziale costruire un sensore cellulare dettagliato in tutto il cervello. Il nostro protocollo di routine ad alto rendimento consente l'analisi della citoarchitettura 3D di aree volumetriche del cervello umano con risoluzione micrometrica, consentendone la caratterizzazione strutturale.

La ricostruzione volumetrica di vaste aree del cervello umano presenta diverse sfide sperimentali legate alle dimensioni massicce dei campioni cerebrali, alla complessa composizione biologica, alle condizioni variabili di fissazione e conservazione post-mortem e ai segnali di autofluorescenza provenienti da pigmenti di tipo lipofuscina. Tutto ciò può compromettere l'efficienza di pulizia ottica e la dimostrazione della qualità. Rispetto ad altre tecniche di clearing, il metodo di trasformazione dei tessuti corti combinato con l'imaging al microscopio a foglio di luce può essere utilizzato per l'elaborazione rapida e simultanea di più sezioni del cervello umano.

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