PUBLICATION

Corpuscles of Stannius development requires FGF signaling

Authors
Klingbeil, K., Nguyen, T., Fahrner, A., Guthmann, C., Wang, H., Schoels, M., Lilienkamp, M., Franz, H., Eckert, P., Walz, G., Yakulov, T.A.
ID
ZDB-PUB-211022-40
Date
2021
Source
Developmental Biology   481: 160-171 (Journal)
Registered Authors
Keywords
Corpuscles of Stannius, Cpe, Development, Fibroblast growth factor (FGF), Kidney, Pronephros, Wnt signaling, Zebrafish
MeSH Terms
  • Animals
  • Cell Differentiation*
  • Endocrine Glands/embryology*
  • Fibroblast Growth Factors*/genetics
  • Fibroblast Growth Factors*/metabolism
  • Glycoproteins/genetics
  • Glycoproteins/metabolism
  • Pronephros/embryology*
  • Wnt Signaling Pathway*
  • Zebrafish*/embryology
  • Zebrafish*/genetics
  • Zebrafish Proteins*/genetics
  • Zebrafish Proteins*/metabolism
PubMed
34666023 Full text @ Dev. Biol.
Abstract
The corpuscles of Stannius (CS) represent a unique endocrine organ of teleostean fish that secrets stanniocalcin-1 (Stc1) to maintain calcium homeostasis. Appearing at 20-25 somite stage in the distal zebrafish pronephros, stc1-expressing cells undergo apical constriction, and are subsequently extruded to form a distinct gland on top of the distal pronephric tubules at 50 h post fertilization (hpf). Several transcription factors (e.g. Hnf1b, Irx3b, Tbx2a/b) and signaling pathways (e.g. Notch) control CS development. We report now that Fgf signaling is required to commit tubular epithelial cells to differentiate into stc1-expressing CS cells. Inhibition of Fgf signaling by SU5402, dominant-negative Fgfr1, or depletion of fgf8a prevented CS formation and stc1 expression. Ablation experiments revealed that CS have the ability to partially regenerate via active cell migration involving extensive filopodia and lamellipodia formation. Activation of Wnt signaling curtailed stc1 expression, but had no effect on CS formation. Thus, our observations identify Fgf signaling as a crucial component of CS cell fate commitment.
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Human Disease / Model
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Mapping