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Diversity in cell motility reveals the dynamic nature of the formation of zebrafish taste sensory organs.

Identifieur interne : 001D24 ( PubMed/Corpus ); précédent : 001D23; suivant : 001D25

Diversity in cell motility reveals the dynamic nature of the formation of zebrafish taste sensory organs.

Auteurs : Marina Soulika ; Anna-Lila Kaushik ; Benjamin Mathieu ; Raquel Lourenço ; Anna Z. Komisarczuk ; Sebastian Alejo Romano ; Adrien Jouary ; Alicia Lardennois ; Nicolas Tissot ; Shinji Okada ; Keiko Abe ; Thomas S. Becker ; Marika Kapsimali

Source :

RBID : pubmed:27122167

English descriptors

Abstract

Taste buds are sensory organs in jawed vertebrates, composed of distinct cell types that detect and transduce specific taste qualities. Taste bud cells differentiate from oropharyngeal epithelial progenitors, which are localized mainly in proximity to the forming organs. Despite recent progress in elucidating the molecular interactions required for taste bud cell development and function, the cell behavior underlying the organ assembly is poorly defined. Here, we used time-lapse imaging to observe the formation of taste buds in live zebrafish larvae. We found that tg(fgf8a.dr17)-expressing cells form taste buds and get rearranged within the forming organs. In addition, differentiating cells move from the epithelium to the forming organs and can be displaced between developing organs. During organ formation, tg(fgf8a.dr17) and type II taste bud cells are displaced in random, directed or confined mode relative to the taste bud they join or by which they are maintained. Finally, ascl1a activity in the 5-HT/type III cell is required to direct and maintain tg(fgf8a.dr17)-expressing cells into the taste bud. We propose that diversity in displacement modes of differentiating cells acts as a key mechanism for the highly dynamic process of taste bud assembly.

DOI: 10.1242/dev.134817
PubMed: 27122167

Links to Exploration step

pubmed:27122167

Le document en format XML

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<div type="abstract" xml:lang="en">Taste buds are sensory organs in jawed vertebrates, composed of distinct cell types that detect and transduce specific taste qualities. Taste bud cells differentiate from oropharyngeal epithelial progenitors, which are localized mainly in proximity to the forming organs. Despite recent progress in elucidating the molecular interactions required for taste bud cell development and function, the cell behavior underlying the organ assembly is poorly defined. Here, we used time-lapse imaging to observe the formation of taste buds in live zebrafish larvae. We found that tg(fgf8a.dr17)-expressing cells form taste buds and get rearranged within the forming organs. In addition, differentiating cells move from the epithelium to the forming organs and can be displaced between developing organs. During organ formation, tg(fgf8a.dr17) and type II taste bud cells are displaced in random, directed or confined mode relative to the taste bud they join or by which they are maintained. Finally, ascl1a activity in the 5-HT/type III cell is required to direct and maintain tg(fgf8a.dr17)-expressing cells into the taste bud. We propose that diversity in displacement modes of differentiating cells acts as a key mechanism for the highly dynamic process of taste bud assembly.</div>
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<Keyword MajorTopicYN="N">Ascl1a</Keyword>
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<Keyword MajorTopicYN="N">Taste bud</Keyword>
<Keyword MajorTopicYN="N">Taste receptor cell</Keyword>
<Keyword MajorTopicYN="N">Time-lapse</Keyword>
<Keyword MajorTopicYN="N">fgf8a</Keyword>
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<Year>2016</Year>
<Month>04</Month>
<Day>12</Day>
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<Year>2017</Year>
<Month>9</Month>
<Day>2</Day>
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