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3 dimensional modelling of early human brain development using optical projection tomography

BACKGROUND: As development proceeds the human embryo attains an ever more complex three dimensional (3D) structure. Analyzing the gene expression patterns that underlie these changes and interpreting their significance depends on identifying the anatomical structures to which they map and following...

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Autores principales: Kerwin, Janet, Scott, Mark, Sharpe, James, Puelles, Luis, Robson, Stephen C, Martínez-de-la-Torre, Margaret, Ferran, Jose Luis, Feng, Guangjie, Baldock, Richard, Strachan, Tom, Davidson, Duncan, Lindsay, Susan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC514604/
https://www.ncbi.nlm.nih.gov/pubmed/15298700
http://dx.doi.org/10.1186/1471-2202-5-27
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author Kerwin, Janet
Scott, Mark
Sharpe, James
Puelles, Luis
Robson, Stephen C
Martínez-de-la-Torre, Margaret
Ferran, Jose Luis
Feng, Guangjie
Baldock, Richard
Strachan, Tom
Davidson, Duncan
Lindsay, Susan
author_facet Kerwin, Janet
Scott, Mark
Sharpe, James
Puelles, Luis
Robson, Stephen C
Martínez-de-la-Torre, Margaret
Ferran, Jose Luis
Feng, Guangjie
Baldock, Richard
Strachan, Tom
Davidson, Duncan
Lindsay, Susan
author_sort Kerwin, Janet
collection PubMed
description BACKGROUND: As development proceeds the human embryo attains an ever more complex three dimensional (3D) structure. Analyzing the gene expression patterns that underlie these changes and interpreting their significance depends on identifying the anatomical structures to which they map and following these patterns in developing 3D structures over time. The difficulty of this task greatly increases as more gene expression patterns are added, particularly in organs with complex 3D structures such as the brain. Optical Projection Tomography (OPT) is a new technology which has been developed for rapidly generating digital 3D models of intact specimens. We have assessed the resolution of unstained neuronal structures within a Carnegie Stage (CS)17 OPT model and tested its use as a framework onto which anatomical structures can be defined and gene expression data mapped. RESULTS: Resolution of the OPT models was assessed by comparison of digital sections with physical sections stained, either with haematoxylin and eosin (H&E) or by immunocytochemistry for GAP43 or PAX6, to identify specific anatomical features. Despite the 3D models being of unstained tissue, peripheral nervous system structures from the trigeminal ganglion (~300 μm by ~150 μm) to the rootlets of cranial nerve XII (~20 μm in diameter) were clearly identifiable, as were structures in the developing neural tube such as the zona limitans intrathalamica (core is ~30 μm thick). Fourteen anatomical domains have been identified and visualised within the CS17 model. Two 3D gene expression domains, known to be defined by Pax6 expression in the mouse, were clearly visible when PAX6 data from 2D sections were mapped to the CS17 model. The feasibility of applying the OPT technology to all stages from CS12 to CS23, which encompasses the major period of organogenesis for the human developing central nervous system, was successfully demonstrated. CONCLUSION: In the CS17 model considerable detail is visible within the developing nervous system at a minimum resolution of ~20 μm and 3D anatomical and gene expression domains can be defined and visualised successfully. The OPT models and accompanying technologies for manipulating them provide a powerful approach to visualising and analysing gene expression and morphology during early human brain development.
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spelling pubmed-5146042004-08-28 3 dimensional modelling of early human brain development using optical projection tomography Kerwin, Janet Scott, Mark Sharpe, James Puelles, Luis Robson, Stephen C Martínez-de-la-Torre, Margaret Ferran, Jose Luis Feng, Guangjie Baldock, Richard Strachan, Tom Davidson, Duncan Lindsay, Susan BMC Neurosci Research Article BACKGROUND: As development proceeds the human embryo attains an ever more complex three dimensional (3D) structure. Analyzing the gene expression patterns that underlie these changes and interpreting their significance depends on identifying the anatomical structures to which they map and following these patterns in developing 3D structures over time. The difficulty of this task greatly increases as more gene expression patterns are added, particularly in organs with complex 3D structures such as the brain. Optical Projection Tomography (OPT) is a new technology which has been developed for rapidly generating digital 3D models of intact specimens. We have assessed the resolution of unstained neuronal structures within a Carnegie Stage (CS)17 OPT model and tested its use as a framework onto which anatomical structures can be defined and gene expression data mapped. RESULTS: Resolution of the OPT models was assessed by comparison of digital sections with physical sections stained, either with haematoxylin and eosin (H&E) or by immunocytochemistry for GAP43 or PAX6, to identify specific anatomical features. Despite the 3D models being of unstained tissue, peripheral nervous system structures from the trigeminal ganglion (~300 μm by ~150 μm) to the rootlets of cranial nerve XII (~20 μm in diameter) were clearly identifiable, as were structures in the developing neural tube such as the zona limitans intrathalamica (core is ~30 μm thick). Fourteen anatomical domains have been identified and visualised within the CS17 model. Two 3D gene expression domains, known to be defined by Pax6 expression in the mouse, were clearly visible when PAX6 data from 2D sections were mapped to the CS17 model. The feasibility of applying the OPT technology to all stages from CS12 to CS23, which encompasses the major period of organogenesis for the human developing central nervous system, was successfully demonstrated. CONCLUSION: In the CS17 model considerable detail is visible within the developing nervous system at a minimum resolution of ~20 μm and 3D anatomical and gene expression domains can be defined and visualised successfully. The OPT models and accompanying technologies for manipulating them provide a powerful approach to visualising and analysing gene expression and morphology during early human brain development. BioMed Central 2004-08-06 /pmc/articles/PMC514604/ /pubmed/15298700 http://dx.doi.org/10.1186/1471-2202-5-27 Text en Copyright © 2004 Kerwin et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kerwin, Janet
Scott, Mark
Sharpe, James
Puelles, Luis
Robson, Stephen C
Martínez-de-la-Torre, Margaret
Ferran, Jose Luis
Feng, Guangjie
Baldock, Richard
Strachan, Tom
Davidson, Duncan
Lindsay, Susan
3 dimensional modelling of early human brain development using optical projection tomography
title 3 dimensional modelling of early human brain development using optical projection tomography
title_full 3 dimensional modelling of early human brain development using optical projection tomography
title_fullStr 3 dimensional modelling of early human brain development using optical projection tomography
title_full_unstemmed 3 dimensional modelling of early human brain development using optical projection tomography
title_short 3 dimensional modelling of early human brain development using optical projection tomography
title_sort 3 dimensional modelling of early human brain development using optical projection tomography
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC514604/
https://www.ncbi.nlm.nih.gov/pubmed/15298700
http://dx.doi.org/10.1186/1471-2202-5-27
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