Transcriptional control of blood cell emergence

FEBS Lett. 2019 Dec;593(23):3304-3315. doi: 10.1002/1873-3468.13585. Epub 2019 Aug 31.

Abstract

The haematopoietic system is established during embryonic life through a series of developmental steps that culminates with the generation of haematopoietic stem cells. Characterisation of the transcriptional network that regulates blood cell emergence has led to the identification of transcription factors essential for this process. Among the many factors wired within this complex regulatory network, ETV2, SCL and RUNX1 are the central components. All three factors are absolutely required for blood cell generation, each one controlling a precise step of specification from the mesoderm germ layer to fully functional blood progenitors. Insight into the transcriptional control of blood cell emergence has been used for devising protocols to generate blood cells de novo, either through reprogramming of somatic cells or through forward programming of pluripotent stem cells. Interestingly, the physiological process of blood cell generation and its laboratory-engineered counterpart have very little in common.

Keywords: embryonic haematopoiesis; haemogenic endothelium; transcription network.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Blood Cells / cytology
  • Blood Cells / metabolism*
  • Cell Differentiation / genetics
  • Cellular Reprogramming / genetics
  • Core Binding Factor Alpha 2 Subunit / genetics*
  • Hematopoietic Stem Cells
  • Humans
  • Mesoderm / growth & development
  • Mesoderm / metabolism
  • Pluripotent Stem Cells / cytology
  • Pluripotent Stem Cells / metabolism
  • T-Cell Acute Lymphocytic Leukemia Protein 1 / genetics*
  • Transcription Factors / genetics*
  • Transcriptional Activation

Substances

  • Core Binding Factor Alpha 2 Subunit
  • ETV2 protein, human
  • RUNX1 protein, human
  • T-Cell Acute Lymphocytic Leukemia Protein 1
  • Transcription Factors
  • TAL1 protein, human