Lifelong haematopoiesis is established by hundreds of precursors throughout mammalian ontogeny

Nat Cell Biol. 2017 Oct;19(10):1153-1163. doi: 10.1038/ncb3607. Epub 2017 Sep 18.

Abstract

Current dogma asserts that mammalian lifelong blood production is established by a small number of blood progenitors. However, this model is based on assays that require the disruption, transplantation and/or culture of embryonic tissues. Here, we used the sample-to-sample variance of a multicoloured lineage trace reporter to assess the frequency of emerging lifelong blood progenitors while avoiding the disruption, culture or transplantation of embryos. We find that approximately 719 Flk1+ mesodermal precursors, 633 VE-cadherin+ endothelial precursors and 545 Vav1+ nascent blood stem and progenitor cells emerge to establish the haematopoietic system at embryonic days (E)7-E8.5, E8.5-E11.5 and E11.5-E14.5, respectively. We also determined that the spatio-temporal recruitment of endothelial blood precursors begins at E8.5 and ends by E10.5, and that many c-Kit+ clusters of newly specified blood progenitors in the aorta are polyclonal in origin. Our work illuminates the dynamics of the developing mammalian blood system during homeostasis.

MeSH terms

  • Animals
  • Antigens, CD / genetics
  • Antigens, CD / metabolism
  • Cadherins / genetics
  • Cadherins / metabolism
  • Cell Differentiation
  • Cell Lineage
  • Cell Tracking / methods
  • Cells, Cultured
  • Coculture Techniques
  • Endothelial Cells / metabolism*
  • Endothelial Cells / transplantation
  • Gene Expression Regulation, Developmental
  • Genotype
  • Gestational Age
  • Hematopoiesis*
  • Hematopoietic Stem Cell Transplantation
  • Hematopoietic Stem Cells / metabolism*
  • Integrases / genetics
  • Integrases / metabolism
  • Linear Models
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Microscopy, Fluorescence
  • Models, Biological
  • Phenotype
  • Proto-Oncogene Proteins c-kit / genetics
  • Proto-Oncogene Proteins c-kit / metabolism
  • Proto-Oncogene Proteins c-vav / genetics
  • Proto-Oncogene Proteins c-vav / metabolism
  • RNA, Untranslated / genetics
  • RNA, Untranslated / metabolism
  • Signal Transduction
  • Time Factors
  • Vascular Endothelial Growth Factor Receptor-2 / genetics
  • Vascular Endothelial Growth Factor Receptor-2 / metabolism

Substances

  • Antigens, CD
  • Cadherins
  • Gt(ROSA)26Sor non-coding RNA, mouse
  • Luminescent Proteins
  • Proto-Oncogene Proteins c-vav
  • RNA, Untranslated
  • Vav1 protein, mouse
  • cadherin 5
  • Kdr protein, mouse
  • Proto-Oncogene Proteins c-kit
  • Vascular Endothelial Growth Factor Receptor-2
  • Cre recombinase
  • Integrases