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Bone Morphogenetic Protein Signaling Restricts Proximodistal Extension of the Ventral Fin Fold
Unpaired fins, which are the most ancient form of locomotory appendages in chordates, had emerged at least 500 million years ago. While it has been suggested that unpaired fins and paired fins share structural similarities, cellular and molecular mechanisms that regulate the outgrowth of the former...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734333/ https://www.ncbi.nlm.nih.gov/pubmed/33330499 http://dx.doi.org/10.3389/fcell.2020.603306 |
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author | Ka, Jun Kim, Jun-Dae Pak, Boryeong Han, Orjin Choi, Woosoung Kim, Hwan Jin, Suk-Won |
author_facet | Ka, Jun Kim, Jun-Dae Pak, Boryeong Han, Orjin Choi, Woosoung Kim, Hwan Jin, Suk-Won |
author_sort | Ka, Jun |
collection | PubMed |
description | Unpaired fins, which are the most ancient form of locomotory appendages in chordates, had emerged at least 500 million years ago. While it has been suggested that unpaired fins and paired fins share structural similarities, cellular and molecular mechanisms that regulate the outgrowth of the former have not been fully elucidated yet. Using the ventral fin fold in zebrafish as a model, here, we investigate how the outgrowth of the unpaired fin is modulated. We show that Bone Morphogenetic Protein (BMP) signaling restricts extension of the ventral fin fold along the proximodistal axis by modulating diverse aspects of cellular behaviors. We find that lack of BMP signaling, either caused by genetic or chemical manipulation, prolongs the proliferative capacity of epithelial cells and substantially increases the number of cells within the ventral fin fold. In addition, inhibition of BMP signaling attenuates the innate propensity of cell division along the anteroposterior axis and shifts the orientation of cell division toward the proximodistal axis. Moreover, abrogating BMP signaling appears to induce excessive distal migration of cells within the ventral fin fold, and therefore precipitates extension along the proximodistal axis. Taken together, our data suggest that BMP signaling restricts the outgrowth of the ventral fin fold during zebrafish development. |
format | Online Article Text |
id | pubmed-7734333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77343332020-12-15 Bone Morphogenetic Protein Signaling Restricts Proximodistal Extension of the Ventral Fin Fold Ka, Jun Kim, Jun-Dae Pak, Boryeong Han, Orjin Choi, Woosoung Kim, Hwan Jin, Suk-Won Front Cell Dev Biol Cell and Developmental Biology Unpaired fins, which are the most ancient form of locomotory appendages in chordates, had emerged at least 500 million years ago. While it has been suggested that unpaired fins and paired fins share structural similarities, cellular and molecular mechanisms that regulate the outgrowth of the former have not been fully elucidated yet. Using the ventral fin fold in zebrafish as a model, here, we investigate how the outgrowth of the unpaired fin is modulated. We show that Bone Morphogenetic Protein (BMP) signaling restricts extension of the ventral fin fold along the proximodistal axis by modulating diverse aspects of cellular behaviors. We find that lack of BMP signaling, either caused by genetic or chemical manipulation, prolongs the proliferative capacity of epithelial cells and substantially increases the number of cells within the ventral fin fold. In addition, inhibition of BMP signaling attenuates the innate propensity of cell division along the anteroposterior axis and shifts the orientation of cell division toward the proximodistal axis. Moreover, abrogating BMP signaling appears to induce excessive distal migration of cells within the ventral fin fold, and therefore precipitates extension along the proximodistal axis. Taken together, our data suggest that BMP signaling restricts the outgrowth of the ventral fin fold during zebrafish development. Frontiers Media S.A. 2020-11-30 /pmc/articles/PMC7734333/ /pubmed/33330499 http://dx.doi.org/10.3389/fcell.2020.603306 Text en Copyright © 2020 Ka, Kim, Pak, Han, Choi, Kim and Jin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Ka, Jun Kim, Jun-Dae Pak, Boryeong Han, Orjin Choi, Woosoung Kim, Hwan Jin, Suk-Won Bone Morphogenetic Protein Signaling Restricts Proximodistal Extension of the Ventral Fin Fold |
title | Bone Morphogenetic Protein Signaling Restricts Proximodistal Extension of the Ventral Fin Fold |
title_full | Bone Morphogenetic Protein Signaling Restricts Proximodistal Extension of the Ventral Fin Fold |
title_fullStr | Bone Morphogenetic Protein Signaling Restricts Proximodistal Extension of the Ventral Fin Fold |
title_full_unstemmed | Bone Morphogenetic Protein Signaling Restricts Proximodistal Extension of the Ventral Fin Fold |
title_short | Bone Morphogenetic Protein Signaling Restricts Proximodistal Extension of the Ventral Fin Fold |
title_sort | bone morphogenetic protein signaling restricts proximodistal extension of the ventral fin fold |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734333/ https://www.ncbi.nlm.nih.gov/pubmed/33330499 http://dx.doi.org/10.3389/fcell.2020.603306 |
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