High-Resolution Episcopic Microscopy (HREM) using the HistoCore NANOCUT R Rotary Microtome by Leica Biosystems

Histological analyses of biological samples represent the gold standard in terms of resolution, image contrast and sensitivity to describe morphological defects. Although laborious and time consuming, this technique is still applied for a lot of analysis requiring structural description. Over the past decades, there has been development of cutting-edge imaging tools to discover novel structural and functional information and imaging has revolutionized biomedical research.

A major driver for the adoption of novel imaging techniques is the specific and varied requirements of individual research groups. For example, in the field of embryonic phenotyping, abnormal morphogenesis of complex developing structures in a developing embryo can be difficult to visualize by external examination or 2D sections of the embryo. Thus, the ability to record three-dimensional (3D) digital images of mutants at different developmental stages by using medium-to-high throughput technologies adds value to the information provided by histology. It allows automated detection of several defects by comparison with wild-type standards as well as the quantification of morphological changes (Adams et al., 2013). Besides the embryology field, examining organ shapes of adult models in 3D stacks can be advantageous because phenotypes can be easier to detect than in 2-dimensional histological sections, particularly for researchers with little anatomical training.

HREM is an effective and powerful tool for assessing structural abnormalities in embryos or organs ex vivo. Essentially ‘3D histology,’ a series of successive 2D images of the sample block face, is captured during histological sectioning of fixed and embedded tissues, providing structural information at high resolution with details approaching those conventionally obtained using histological analysis. HREM data can be analysed either as 2D image stacks or by 3D rendering and they can reveal alterations in morphology that are impossible to detect using lower resolution techniques such as micro-CT or MRI. The voxel resolution of 3D models is only limited by the thickness of sections successively removed from the block surface. In practice, spatial resolutions of 1µm are standard (Weninger et al., 2006; Weninger and Mohun, 2002).

The accuracy of image alignment critically depends on the block face returning precisely to the same position for photography after each section cycle. This specification is not standard for rotary microtomes, which require modifications to ensure this capability. Some sledge microtomes were engineered to possess suitably precise stopping positions for photography (e.g., Leica SM2500), but they are no longer commercialized. Recently, Leica Biosystems developed a new rotary microtome HistoCore NANOCUT R that can be coupled with the optics and camera.

Principle of the Procedure

Phenotyping mouse embryos or organs using HREM requires the sample to be embedded in resin. Samples are gradually dehydrated in ethanol, before being embedded in JB4 resin to produce a block suitable for cutting. In order to produce contrast, the embedding resin is completed with Eosin B (emits fluorescence when mixed in JB4) and Acridine Orange (absorbs Eosin signal and creates contrast). Eosin staining is well known from histology and Acridine Orange has a strong affinity for nucleus, resulting in a contrast that strongly resemble to a grayscale capture of Hematoxylin & Eosin staining.

The embedded sample are placed on the HREM HistoCore NANOCUT R’s microtome by Leica Biosystems and lit with blue light (450-500 nm range) to acquire an image, then a slice is cut from the block to remove matter and the process is repeated. As the concentration of Eosin in the resin is very high, excitation light is absorbed within a micrometer from the block’s surface. This effect allows you to consider the images obtained from HREM as surface data (the data collected will be restricted to a depth below 1µm, and thus will never exceed the thickness of the section ≥ 1µm). The thickness of the sections will be adjusted to the pixel size of the images in order to obtain isotropic voxels (same size in x, y, z dimensions).

The result is a series of images taken across the sample that can be used to reconstruct image data in 3D, allowing you to examine a slice in any orientation within the stack without loss of quality.

Please note that HREM processing is destructive, the sample being cut into sections, and that one sample can therefore only be imaged once. This makes the initial setup of the sample critical to get optimal images that will serve sample analysis the best.

Materials

• Biological material: Mouse embryos or fetuses, pieces of adult tissues no larger than 20 mm.
• Bouin’s fixative
• JB-4 resin embedding kit (Polysciences, Inc.)
• Eosin B (Sigma-Aldrich)
• Acridine Orange (Sigma-Aldrich)
• Ethanol 100% and a series of 70%, 80%, 90%, 95% in H2O
• Polyethylene embedding molds
• TC-65 Tungsten Carbide blades (Leica Biosystems)

Sample Embedding

This protocol is simplified to illustrate the basics of the procedure. For detailed protocol see https://dmdd.org.uk/hrem/sample-preparation/

• Fix the specimens in Bouin’s fixative
• Wash in graded ethanol solutions: 70%, 80%, 90%, 95%, 100%
• Prepare JB4 resin mixture containing Acridine orange and eosin.
• Incubate in mixed resin/ethanol (1:1)
• Incubate in pure resin mixture
• Prepare fresh activated JB4 resin
• Polymerize a cushion in the bottom of the mould
• Place the sample on the cushion in the mould containing activated resin and polymerize the resin at 4°C overnight. The resin is covered with mineral oil to avoid contact with the air.
• Further harden the block in an oven at 95°C

Locate the sample within the block using an oblique illumination and trim the resin that does not contain the specimen (will permit to adjust at the better magnification)

• Mount the block on the HistoCore NANOCUT R microtome by Leica Biosystems
• Use 3D mode of the microtome
• Trim block until the very beginning of the specimen
• Adjust the focus
• Start the automated sectioning and image capture. Special adapted software modules (MetaMorph® Software or home-made software available upon request) will permit the synchronization of cutting and image capturing.
• Sections can be performed from 2µm to 7µm. As an example, embryos at E15.5 stage are cut at 7µm.
• For data processing, optimize grayscale mapping as desired; scale data and/or subsample as appropriate for 3D rendering software.

A. Prototype Apparatus for Episcopic Imaging

The HREM prototype is composed of a camera SCMOS, a GFP- fluorescence filter, a LED light source, optical device (macroscope), a mirror, the knife holder and the sample mounted on the HistoCore NANOCUT Rotary microtome by Leica Biosystems.

The development of the HistoCore NANOCUT R microtome by Leica Biosystems with a 3D option is of great interest to people who wish to develop HREM technology in their laboratory. Performing automated sections using the Leica HistoCore NANOCUT R microtome led to increased reproducibility of key parameters like the cutting surface and precise positioning of the block leading to perfect alignment of the sections and enhanced quality of 3D reconstructions.

HREM digital images offer several advantages compared to conventional histological sections. Firstly, they do not show distortions introduced by the sectioning, section processing or mounting processes. Furthermore, a series of thousands of images are produced within a few hours in an automated way in contrast to weeks to produce a series of more or less precisely realigned digital images from a thousands of histological sections. HREM volume data can be immediately analysed with orthogonal and oblique virtual re-sectioning tools and appropriate software.

HREM has proved to be an excellent tool in a broad variety of research fields. In addition to the increasing use of HREM for visualizing embryos for screening the phenotype of prenatally lethal E14.5/E15.5 mouse embryos produced for the International Mouse Phenotyping Consortium (IMPC) (Dickinson at al., 2016),it was very recently also employed for visualizing tissue samples of adult biomedical model organisms (Weninger et al., 2013; Geyer et al., 2015), human skin biopsies (Tinhofer et al., 2018) and biological materials used in modern medicine. The highly encouraging results lead us to the conclusion that HREM has the potential to become a valuable tool in various fields of pre- and clinical research within the next decade.

Therefore, HREM offers low-cost and high-quality information using readily available laboratory equipment, which is particularly important for individual researchers.

We thank Dr T. Mohun and W.J. Weninger for a constructive discussion and their help in the initial step of this project. The project was supported by the French state funds through the “Agence Nationale de la Recherche” under the frame programme “Investissements d’Avenir” labelled (ANR-10-IDEX-0002-02, ANR-10-LABX-0030-INRT, ANR-10-INBS-07 PHENOMIN).

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The following research was prepared by an independent third-party on behalf of Leica Biosystems. Leica Biosystems was not involved in preparing this research, which reflects an independent, outside opinion.

Olivia Wendling^1-5, Didier Hentsch^1-4, Fabien Pertuy^1-5, Hugues Jacobs^1-5, Nicolas Lemercier ^1-4, Serge Taubert^{1- 4} Jean-Luc Vonesch^1-4, Patrick Reilly^1-5, Bertrand Séraphin^1-4, and Yann Hérault^1-5

1. Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, France
2. Centre National de la Recherche Scientifique, UMR7104, Illkirch, France
3. Institut National de la Santé et de la Recherche Médicale, U1258, Illkirch, France
4. Université de Strasbourg, Illkirch, France
5. ICS Infrastructure, Illkirch, France