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Abstract
Tight junctions (TJs) function as a physiological barrier between epithelial and endothelial sheets by restricting the diffusion of fluid through the intercellular space. Recent morphological studies associated with TJs have revealed that the TJ is a dynamic rather than a static structure; indeed, several in vitro studies indicate that proper TJ function requires dynamic TJ behavior. Direct observation of the dynamic behavior of TJs is necessary to understand the essential roles of TJs in physiological contexts, such as during embryogenesis and metastasis. Here we describe a protocol for the generation of transgenic medaka (Oryzias latipes) that express claudin–EGFP. This fluorescent fusion protein enables real-time imaging of TJs in the living embryo. Claudin–EGFP transgenic medaka will be a useful tool to screen for mutations and for small molecules affecting cell–cell adhesion.
Original language | English |
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Title of host publication | Claudins |
Subtitle of host publication | Methods in Molecular Biology |
Editors | Turksen Kursad |
Place of Publication | New York |
Publisher | Humana Press |
Pages | 171-178 |
Number of pages | 8 |
Volume | 762 |
ISBN (Print) | 9781617791857 |
DOIs | |
Publication status | Published - 2011 |
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Dive into the research topics of 'In vivo imaging of tight junctions using claudin-EGFP transgenic medaka'. Together they form a unique fingerprint.Projects
- 1 Finished
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CELLULAR AND GENETIC ANALYSIS OF LIVER DISEASE AND REGENERAT ION MODELS IN FISH
Furutani-Seiki, M. (PI)
30/03/07 → 29/03/12
Project: Research council