Interactions between mural cells and endothelial cells stabilize the developing zebrafish dorsal aorta

Amber N. Stratman, Sofia A. Pezoa, Olivia M. Farrelly, Daniel Castranova, Louis E. Dye, Matthew G. Butler, Harwin Sidik, William S. Talbot, Brant M. Weinstein

Research output: Contribution to journalArticle

26 Scopus citations

Abstract

Mural cells (vascular smooth muscle cells and pericytes) play an essential role in the development of the vasculature, promoting vascular quiescence and long-term vessel stabilization through their interactions with endothelial cells. However, the mechanistic details of how mural cells stabilize vessels are not fully understood.We have examined the emergence and functional role of mural cells investing the dorsal aorta during early development using the zebrafish. Consistent with previous literature, our data suggest that cells ensheathing the dorsal aorta emerge from a sub-population of cells in the adjacent sclerotome. Inhibition of mural cell recruitment to the dorsal aorta through disruption of pdgfr signaling leads to a reduced vascular basement membrane, which in turn results in enhanced dorsal aorta vessel elasticity and failure to restrict aortic diameter. Our results provide direct in vivo evidence for a functional role for mural cells in patterning and stabilization of the early vasculature through production and maintenance of the vascular basement membrane to prevent abnormal aortic expansion and elasticity.

Original languageEnglish
Pages (from-to)115-127
Number of pages13
JournalDevelopment (Cambridge)
Volume144
Issue number1
DOIs
StatePublished - Jan 1 2017
Externally publishedYes

Keywords

  • PDGFR signaling
  • Pericyte
  • Vascular basement membrane
  • Vascular smooth muscle
  • Zebrafish

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    Stratman, A. N., Pezoa, S. A., Farrelly, O. M., Castranova, D., Dye, L. E., Butler, M. G., Sidik, H., Talbot, W. S., & Weinstein, B. M. (2017). Interactions between mural cells and endothelial cells stabilize the developing zebrafish dorsal aorta. Development (Cambridge), 144(1), 115-127. https://doi.org/10.1242/dev.143131