Abstract
Imaging is a method of choice to investigate the complex spatio-temporal cellular dynamics and the signalling pathways that control them during development. The ability to tag many proteins in vivo makes it possible to analyse the detailed dynamics of these interactions ranging over several orders of magnitude; from the study of single molecule events on the millisecond and nanometre scale up to the complex three-dimensional behaviour of cells in tissues on the millimetre scale over time periods of hours to days. Great advances are being made in the detailed study of molecular processes using high resolution imaging techniques in transparent samples close to the surface of cells or tissues, where light scattering is minimal. The major challenge is to translate some of these methods to the study of cells and tissues in their native 3D environment. These imaging methods require novel and innovative analysis methods to fully exploit the information available in these data. We will illustrate some of these points in the investigation of the development of the cellular slime mould Dictyostelium discoideum and the study of cell behaviours during gastrulation in the chick embryo. Crown Copyright (C) 2009 Published by Elsevier Ltd. All rights reserved.
Original language | English |
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Pages (from-to) | 947-955 |
Number of pages | 9 |
Journal | Seminars in Cell & Developmental Biology |
Volume | 20 |
Issue number | 8 |
DOIs | |
Publication status | Published - Oct 2009 |
Keywords
- Dictyostelium
- Signalling
- Cell movement
- Chemotaxis
- Gastrulation
- Imaging
- Primitive streak form
- Single molecule analysis
- Dictostelium discoideum
- Chick embryo
- In vivo
- Simultaneous quantification
- Nuclear translocation
- STAT protein
- Motile cells
- Tissue flow