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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...

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Autores principales: Ka, Jun, Kim, Jun-Dae, Pak, Boryeong, Han, Orjin, Choi, Woosoung, Kim, Hwan, Jin, Suk-Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
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.
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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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