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Advanced optical imaging in living embryos

Developmental biology investigations have evolved from static studies of embryo anatomy and into dynamic studies of the genetic and cellular mechanisms responsible for shaping the embryo anatomy. With the advancement of fluorescent protein fusions, the ability to visualize and comprehend how thousan...

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Detalles Bibliográficos
Autores principales: Canaria, Christie A., Lansford, Rusty
Formato: Texto
Lenguaje:English
Publicado: SP Birkhäuser Verlag Basel 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2943067/
https://www.ncbi.nlm.nih.gov/pubmed/20614161
http://dx.doi.org/10.1007/s00018-010-0440-5
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author Canaria, Christie A.
Lansford, Rusty
author_facet Canaria, Christie A.
Lansford, Rusty
author_sort Canaria, Christie A.
collection PubMed
description Developmental biology investigations have evolved from static studies of embryo anatomy and into dynamic studies of the genetic and cellular mechanisms responsible for shaping the embryo anatomy. With the advancement of fluorescent protein fusions, the ability to visualize and comprehend how thousands to millions of cells interact with one another to form tissues and organs in three dimensions (xyz) over time (t) is just beginning to be realized and exploited. In this review, we explore recent advances utilizing confocal and multi-photon time-lapse microscopy to capture gene expression, cell behavior, and embryo development. From choosing the appropriate fluorophore, to labeling strategy, to experimental set-up, and data pipeline handling, this review covers the various aspects related to acquiring and analyzing multi-dimensional data sets. These innovative techniques in multi-dimensional imaging and analysis can be applied across a number of fields in time and space including protein dynamics to cell biology to morphogenesis.
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spelling pubmed-29430672010-10-12 Advanced optical imaging in living embryos Canaria, Christie A. Lansford, Rusty Cell Mol Life Sci Review Developmental biology investigations have evolved from static studies of embryo anatomy and into dynamic studies of the genetic and cellular mechanisms responsible for shaping the embryo anatomy. With the advancement of fluorescent protein fusions, the ability to visualize and comprehend how thousands to millions of cells interact with one another to form tissues and organs in three dimensions (xyz) over time (t) is just beginning to be realized and exploited. In this review, we explore recent advances utilizing confocal and multi-photon time-lapse microscopy to capture gene expression, cell behavior, and embryo development. From choosing the appropriate fluorophore, to labeling strategy, to experimental set-up, and data pipeline handling, this review covers the various aspects related to acquiring and analyzing multi-dimensional data sets. These innovative techniques in multi-dimensional imaging and analysis can be applied across a number of fields in time and space including protein dynamics to cell biology to morphogenesis. SP Birkhäuser Verlag Basel 2010-07-08 2010 /pmc/articles/PMC2943067/ /pubmed/20614161 http://dx.doi.org/10.1007/s00018-010-0440-5 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Review
Canaria, Christie A.
Lansford, Rusty
Advanced optical imaging in living embryos
title Advanced optical imaging in living embryos
title_full Advanced optical imaging in living embryos
title_fullStr Advanced optical imaging in living embryos
title_full_unstemmed Advanced optical imaging in living embryos
title_short Advanced optical imaging in living embryos
title_sort advanced optical imaging in living embryos
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2943067/
https://www.ncbi.nlm.nih.gov/pubmed/20614161
http://dx.doi.org/10.1007/s00018-010-0440-5
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