Artefacts in Volume Data Generated with High Resolution Episcopic Microscopy (HREM)

High resolution episcopic microscopy (HREM) produces digital volume data by physically sectioning histologically processed specimens, while capturing images of the subsequently exposed block faces. Our study aims to systematically define the spectrum of typical artefacts inherent to HREM data and to...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Lukas F. Reissig, Stefan H. Geyer, Julia Rose, Fabrice Prin, Robert Wilson, Dorota Szumska, Antonella Galli, Catherine Tudor, Jacqueline K. White, Tim J. Mohun, Wolfgang J. Weninger
Formato: article
Lenguaje:EN
Publicado: MDPI AG 2021
Materias:
Acceso en línea:https://doaj.org/article/ca09480fece248ccbc47be14e028a050
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:ca09480fece248ccbc47be14e028a050
record_format dspace
spelling oai:doaj.org-article:ca09480fece248ccbc47be14e028a0502021-11-25T16:51:06ZArtefacts in Volume Data Generated with High Resolution Episcopic Microscopy (HREM)10.3390/biomedicines91117112227-9059https://doaj.org/article/ca09480fece248ccbc47be14e028a0502021-11-01T00:00:00Zhttps://www.mdpi.com/2227-9059/9/11/1711https://doaj.org/toc/2227-9059High resolution episcopic microscopy (HREM) produces digital volume data by physically sectioning histologically processed specimens, while capturing images of the subsequently exposed block faces. Our study aims to systematically define the spectrum of typical artefacts inherent to HREM data and to research their effect on the interpretation of the phenotype of wildtype and mutant mouse embryos. A total of 607 (198 wildtypes, 409 mutants) HREM data sets of mouse embryos harvested at embryonic day (E) 14.5 were systematically and comprehensively examined. The specimens had been processed according to essentially identical protocols. Each data set comprised 2000 to 4000 single digital images. Voxel dimensions were 3 × 3 × 3 µm<sup>3</sup>. Using 3D volume models and virtual resections, we identified a number of characteristic artefacts and grouped them according to their most likely causality. Furthermore, we highlight those that affect the interpretation of embryo data and provide examples for artefacts mimicking tissue defects and structural pathologies. Our results aid in optimizing specimen preparation and data generation, are vital for the correct interpretation of HREM data and allow distinguishing tissue defects and pathologies from harmless artificial alterations. In particular, they enable correct diagnosis of pathologies in mouse embryos serving as models for deciphering the mechanisms of developmental disorders.Lukas F. ReissigStefan H. GeyerJulia RoseFabrice PrinRobert WilsonDorota SzumskaAntonella GalliCatherine TudorJacqueline K. WhiteTim J. MohunWolfgang J. WeningerMDPI AGarticleHREMartefactsblock face imaginghistologyembryogenetically engineeredBiology (General)QH301-705.5ENBiomedicines, Vol 9, Iss 1711, p 1711 (2021)
institution DOAJ
collection DOAJ
language EN
topic HREM
artefacts
block face imaging
histology
embryo
genetically engineered
Biology (General)
QH301-705.5
spellingShingle HREM
artefacts
block face imaging
histology
embryo
genetically engineered
Biology (General)
QH301-705.5
Lukas F. Reissig
Stefan H. Geyer
Julia Rose
Fabrice Prin
Robert Wilson
Dorota Szumska
Antonella Galli
Catherine Tudor
Jacqueline K. White
Tim J. Mohun
Wolfgang J. Weninger
Artefacts in Volume Data Generated with High Resolution Episcopic Microscopy (HREM)
description High resolution episcopic microscopy (HREM) produces digital volume data by physically sectioning histologically processed specimens, while capturing images of the subsequently exposed block faces. Our study aims to systematically define the spectrum of typical artefacts inherent to HREM data and to research their effect on the interpretation of the phenotype of wildtype and mutant mouse embryos. A total of 607 (198 wildtypes, 409 mutants) HREM data sets of mouse embryos harvested at embryonic day (E) 14.5 were systematically and comprehensively examined. The specimens had been processed according to essentially identical protocols. Each data set comprised 2000 to 4000 single digital images. Voxel dimensions were 3 × 3 × 3 µm<sup>3</sup>. Using 3D volume models and virtual resections, we identified a number of characteristic artefacts and grouped them according to their most likely causality. Furthermore, we highlight those that affect the interpretation of embryo data and provide examples for artefacts mimicking tissue defects and structural pathologies. Our results aid in optimizing specimen preparation and data generation, are vital for the correct interpretation of HREM data and allow distinguishing tissue defects and pathologies from harmless artificial alterations. In particular, they enable correct diagnosis of pathologies in mouse embryos serving as models for deciphering the mechanisms of developmental disorders.
format article
author Lukas F. Reissig
Stefan H. Geyer
Julia Rose
Fabrice Prin
Robert Wilson
Dorota Szumska
Antonella Galli
Catherine Tudor
Jacqueline K. White
Tim J. Mohun
Wolfgang J. Weninger
author_facet Lukas F. Reissig
Stefan H. Geyer
Julia Rose
Fabrice Prin
Robert Wilson
Dorota Szumska
Antonella Galli
Catherine Tudor
Jacqueline K. White
Tim J. Mohun
Wolfgang J. Weninger
author_sort Lukas F. Reissig
title Artefacts in Volume Data Generated with High Resolution Episcopic Microscopy (HREM)
title_short Artefacts in Volume Data Generated with High Resolution Episcopic Microscopy (HREM)
title_full Artefacts in Volume Data Generated with High Resolution Episcopic Microscopy (HREM)
title_fullStr Artefacts in Volume Data Generated with High Resolution Episcopic Microscopy (HREM)
title_full_unstemmed Artefacts in Volume Data Generated with High Resolution Episcopic Microscopy (HREM)
title_sort artefacts in volume data generated with high resolution episcopic microscopy (hrem)
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/ca09480fece248ccbc47be14e028a050
work_keys_str_mv AT lukasfreissig artefactsinvolumedatageneratedwithhighresolutionepiscopicmicroscopyhrem
AT stefanhgeyer artefactsinvolumedatageneratedwithhighresolutionepiscopicmicroscopyhrem
AT juliarose artefactsinvolumedatageneratedwithhighresolutionepiscopicmicroscopyhrem
AT fabriceprin artefactsinvolumedatageneratedwithhighresolutionepiscopicmicroscopyhrem
AT robertwilson artefactsinvolumedatageneratedwithhighresolutionepiscopicmicroscopyhrem
AT dorotaszumska artefactsinvolumedatageneratedwithhighresolutionepiscopicmicroscopyhrem
AT antonellagalli artefactsinvolumedatageneratedwithhighresolutionepiscopicmicroscopyhrem
AT catherinetudor artefactsinvolumedatageneratedwithhighresolutionepiscopicmicroscopyhrem
AT jacquelinekwhite artefactsinvolumedatageneratedwithhighresolutionepiscopicmicroscopyhrem
AT timjmohun artefactsinvolumedatageneratedwithhighresolutionepiscopicmicroscopyhrem
AT wolfgangjweninger artefactsinvolumedatageneratedwithhighresolutionepiscopicmicroscopyhrem
_version_ 1718412923578089472