Cryo‐SEM in haematological research

Cryogenic scanning electron microscopy (cryo-SEM) is a powerful imaging technique used in cellular biology, providing high-resolution micrographs that show the complexity and dynamics of biological systems. The use of high-pressure freezing (HPF) for specimen fixation preserves cellular structures in their native, hydrated state, avoiding the artefacts introduced by conventional chemical fixation, while modern microscopes provide high-resolution imaging at low electron acceleration voltage, giving fine structural details. That makes cryo-SEM a unique tool for understanding cellular complexity. However, operating the SEM at cryogenic conditions requires careful optimisation of working parameters to avoid artefacts. In our work, we explore the potential of cryo-SEM for haematology and general cell studies. We discuss the impact of a combination of different signals and work distance on specimen appearance and present examples of studies on healthy human blood cells under physiological conditions. Our findings illustrate the breadth of information that can be obtained from these data, highlighting the technique's capacity to enhance our understanding of cellular biology.

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Publication Details

Journal
Journal of Microscopy
Published
2025-05-09
DOI
https://doi.org/10.1111/jmi.13424
Citations
2
Primary Topic
Advanced Electron Microscopy Techniques and Applications
Type
article
Field-Weighted Citation Impact
5.10
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article

Cryo‐SEM in haematological research

Carina Levin, Yeshayahu Talmon, Irina Davidovich
2 citations
Journal of Microscopy
Advanced Electron Microscopy Techniques and Applications
5.10
article

Cryo‐SEM in haematological research

Carina Levin, Yeshayahu Talmon, Irina Davidovich
article en
2 citations

Abstract

Cryogenic scanning electron microscopy (cryo-SEM) is a powerful imaging technique used in cellular biology, providing high-resolution micrographs that show the complexity and dynamics of biological systems. The use of high-pressure freezing (HPF) for specimen fixation preserves cellular structures in their native, hydrated state, avoiding the artefacts introduced by conventional chemical fixation, while modern microscopes provide high-resolution imaging at low electron acceleration voltage, giving fine structural details. That makes cryo-SEM a unique tool for understanding cellular complexity. However, operating the SEM at cryogenic conditions requires careful optimisation of working parameters to avoid artefacts. In our work, we explore the potential of cryo-SEM for haematology and general cell studies. We discuss the impact of a combination of different signals and work distance on specimen appearance and present examples of studies on healthy human blood cells under physiological conditions. Our findings illustrate the breadth of information that can be obtained from these data, highlighting the technique's capacity to enhance our understanding of cellular biology.

Journal of MicroscopyVol. 299(2)
Technion – Israel Institute of Technology (IL), Emek Medical Center (IL)
Openalex Percentile: Top 6%
Advanced Electron Microscopy Techniques and Applications
5.10
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