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Related Concept Videos

Imaging Biological Samples with Optical Microscopy01:18

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Optical microscopy uses optic principles to provide detailed images of samples. Antonie van Leeuwenhoek designed the first compound optical microscope in the 17th century to visualize blood cells, bacteria, and yeast cells. In 1830, Joseph Jackson Lister created an essentially modern light microscope. The 20th century saw the development of microscopes with enhanced magnification and resolution.
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The wavelengths of visible light ultimately limit the maximum theoretical resolution of images created by light microscopes. Most light microscopes can only magnify 1000X, and a few can magnify up to 1500X. Electrons, like electromagnetic radiation, can behave like waves, but with wavelengths of 0.005 nm, they produce significantly greater resolution up to 0.05 nm as compared to 500 nm for visible light. An electron microscope (EM) can create a sharp image that is magnified up to 2,000,000X.
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Rapid Acquisition of 3D Images Using High-resolution Episcopic Microscopy
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Artefacts in Volume Data Generated with High Resolution Episcopic Microscopy (HREM).

Lukas F Reissig1, Stefan H Geyer1, Julia Rose1

  • 1Division of Anatomy, Center for Anatomy and Cell Biology, Medical University of Vienna, 1090 Vienna, Austria.

Biomedicines
|November 27, 2021
PubMed
Summary
This summary is machine-generated.

High resolution episcopic microscopy (HREM) generates digital embryo data. This study defines HREM artifacts, crucial for accurately diagnosing developmental disorders in mouse models.

Keywords:
HREMartefactsblock face imagingembryogenetically engineeredhistologymouse embryo

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Area of Science:

  • Developmental Biology
  • Microscopy Techniques
  • Bioimaging

Background:

  • High resolution episcopic microscopy (HREM) is a powerful technique for generating 3D digital volume data of biological specimens.
  • Accurate interpretation of HREM data is essential for studying embryonic development and disease models.

Purpose of the Study:

  • To systematically identify and characterize artifacts in HREM data of mouse embryos.
  • To assess the impact of these artifacts on the interpretation of wildtype and mutant phenotypes.
  • To provide guidance for optimizing HREM specimen preparation and data analysis.

Main Methods:

  • Examination of 607 HREM datasets from mouse embryos (E14.5), including wildtypes and mutants.
  • Systematic analysis of digital images (2000-4000 per dataset) with voxel dimensions of 3 × 3 × 3 µm³.
  • Utilized 3D volume models and virtual resections to identify and classify artifacts.

Main Results:

  • A comprehensive spectrum of characteristic HREM artifacts was identified and categorized by causality.
  • Specific artifacts were highlighted for their potential to mimic genuine tissue defects and structural pathologies.
  • Examples were provided to illustrate how artifacts can lead to misinterpretation of embryonic phenotypes.

Conclusions:

  • Understanding HREM artifacts is vital for accurate phenotyping of mouse embryos.
  • Distinguishing artifacts from true pathologies ensures correct diagnosis of developmental disorders.
  • Optimized HREM protocols and data interpretation aid in deciphering mechanisms of developmental disorders.