Bone Morphogenetic Protein Signaling Restricts Proximodistal Extension of the Ventral Fin Fold.

Jun Ka, Jun-Dae Kim, Boryeong Pak, Orjin Han, Woosoung Choi, Hwan Kim, Suk-Won Jin
Author Information
  1. Jun Ka: School of Life Sciences, Cell Logistics Research Center, Gwangju Institute of Science and Technology, Gwangju, South Korea.
  2. Jun-Dae Kim: Yale Cardiovascular Research Center, Section of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, United States.
  3. Boryeong Pak: School of Life Sciences, Cell Logistics Research Center, Gwangju Institute of Science and Technology, Gwangju, South Korea.
  4. Orjin Han: School of Life Sciences, Cell Logistics Research Center, Gwangju Institute of Science and Technology, Gwangju, South Korea.
  5. Woosoung Choi: School of Life Sciences, Cell Logistics Research Center, Gwangju Institute of Science and Technology, Gwangju, South Korea.
  6. Hwan Kim: Gwangju Institute of Science and Technology, Central Research Facilities, Gwangju, South Korea.
  7. Suk-Won Jin: School of Life Sciences, Cell Logistics Research Center, Gwangju Institute of Science and Technology, Gwangju, South Korea.

Abstract

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.

Keywords

References

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