BMP signaling restricts hemato-vascular development from lateral mesoderm during somitogenesis

Development. 2006 Jun;133(11):2177-87. doi: 10.1242/dev.02386. Epub 2006 May 3.

Abstract

The bone morphogenetic protein (BMP) signaling pathway is essential during gastrulation for the generation of ventral mesoderm, which makes it a challenge to define functions for this pathway at later stages of development. We have established an approach to disrupt BMP signaling specifically in lateral mesoderm during somitogenesis, by targeting a dominant-negative BMP receptor to Lmo2+ cells in developing zebrafish embryos. This results in expansion of hematopoietic and endothelial cells, while restricting the expression domain of the pronephric marker pax2.1. Expression of a constitutively active receptor and transplantation experiments were used to confirm that BMP signaling in lateral mesoderm restricts subsequent hemato-vascular development. The results show that the BMP signaling pathway continues to function after cells are committed to a lateral mesoderm fate, and influences subsequent lineage decisions by restricting hemato-vascular fate in favor of pronephric development.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Biomarkers
  • Bone Morphogenetic Protein Receptors / genetics
  • Bone Morphogenetic Protein Receptors / metabolism
  • Bone Morphogenetic Proteins / metabolism*
  • Deoxyribonucleases, Type II Site-Specific / genetics
  • Deoxyribonucleases, Type II Site-Specific / metabolism
  • Gene Expression Regulation, Developmental
  • Hematopoiesis*
  • Kidney / blood supply
  • Kidney / embryology
  • Kidney / metabolism
  • Mesoderm / metabolism*
  • PAX2 Transcription Factor / metabolism
  • Saccharomyces cerevisiae Proteins
  • Signal Transduction*
  • Somites / metabolism*
  • Stem Cells / metabolism
  • Time Factors
  • Zebrafish / embryology
  • Zebrafish / genetics
  • Zebrafish / metabolism
  • Zebrafish Proteins / metabolism

Substances

  • Biomarkers
  • Bone Morphogenetic Proteins
  • PAX2 Transcription Factor
  • Saccharomyces cerevisiae Proteins
  • Zebrafish Proteins
  • pax2a protein, zebrafish
  • Bone Morphogenetic Protein Receptors
  • SCEI protein, S cerevisiae
  • Deoxyribonucleases, Type II Site-Specific