4.6 Article

Molecular characteristics of the edge cells responsible for expansion of the chick embryo on the vitelline membrane

Journal

OPEN BIOLOGY
Volume 12, Issue 9, Pages -

Publisher

ROYAL SOC
DOI: 10.1098/rsob.220147

Keywords

cell polarity; epithelial sheet fusion; epithelial-mesenchymal transition (EMT); mesenchyme-epithelial transition (MET)

Funding

  1. Wellcome Trust Investigator Award [107055/Z/15/Z]
  2. Wellcome Trust award
  3. National Research Foundation of Korea(NRF) - Ministry of Education [2014R1A6A3A03053468]
  4. Ministry of Education of Saudi Arabia [SE-12267]
  5. National Research Foundation of Korea [2014R1A6A3A03053468] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  6. Wellcome Trust [107055/Z/15/Z] Funding Source: Wellcome Trust

Ask authors/readers for more resources

During avian development, the edge cells play a crucial role in blastoderm expansion. This study explores the morphology and molecular properties of the edge cells in chick embryos and uncovers distinct sub-regions within the edge. Live imaging reveals dynamic cellular activity at the leading edge of the outermost cells. The findings suggest that edge cells could serve as a valuable model system for studying wound healing and closure events in epithelial cell sheets.
During early avian development, only a narrow band of cells (the edge cells, also called 'margin of overgrowth') at the rim of the embryo is responsible for blastoderm expansion by crawling over the vitelline membrane (VM) to cover the whole egg yolk in just 4 days (a process called epiboly). Surprisingly, this has not yet been studied in detail. Here we explore the edge cells of the chick embryo using in situ hybridization, immunohistochemistry and live imaging. Morphological and molecular properties reveal that the edge has a distinctive structure, being subdivided into sub-regions, including at least four distinct zones (which we name as leading, trailing, deep and stalk zones). This allows us to study reorganization of the edge region that accompanies reattachment of an explanted blastoderm to the VM. Immunohistochemistry uncovers distinct polarized cellular features resembling the process of collective cell migration described in other systems. Live imaging reveals dynamic lamellipodial and filopodial activity at the leading edge of the outermost cells. Our data provide evidence that edge cells are a distinct tissue. We propose that edge cells may be a useful model system for the study of wound healing and other closure events in epithelial cell sheets.

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