Distinct mesoderm migration phenotypes in extra-embryonic and embryonic regions of the early mouse embryo.
Bechara SaykaliNavrita MathiahWallis NahabooMarie-Lucie RacuLatifa HammouMatthieu DefranceIsabelle MigeottePublished in: eLife (2019)
In mouse embryo gastrulation, epiblast cells delaminate at the primitive streak to form mesoderm and definitive endoderm, through an epithelial-mesenchymal transition. Mosaic expression of a membrane reporter in nascent mesoderm enabled recording cell shape and trajectory through live imaging. Upon leaving the streak, cells changed shape and extended protrusions of distinct size and abundance depending on the neighboring germ layer, as well as the region of the embryo. Embryonic trajectories were meandrous but directional, while extra-embryonic mesoderm cells showed little net displacement. Embryonic and extra-embryonic mesoderm transcriptomes highlighted distinct guidance, cytoskeleton, adhesion, and extracellular matrix signatures. Specifically, intermediate filaments were highly expressed in extra-embryonic mesoderm, while live imaging for F-actin showed abundance of actin filaments in embryonic mesoderm only. Accordingly, Rhoa or Rac1 conditional deletion in mesoderm inhibited embryonic, but not extra-embryonic mesoderm migration. Overall, this indicates separate cytoskeleton regulation coordinating the morphology and migration of mesoderm subpopulations.
Keyphrases
- pluripotent stem cells
- induced apoptosis
- epithelial mesenchymal transition
- extracellular matrix
- high resolution
- stem cells
- signaling pathway
- oxidative stress
- poor prognosis
- escherichia coli
- cell migration
- cystic fibrosis
- endoplasmic reticulum stress
- mass spectrometry
- dna methylation
- photodynamic therapy
- microbial community
- rectal cancer