PUBLICATION

Endothelial-to-hematopoietic transition: Notch-ing vessels into blood

Authors
Kanz, D., Konantz, M., Alghisi, E., North, T.E., Lengerke, C.
ID
ZDB-PUB-160326-1
Date
2016
Source
Annals of the New York Academy of Sciences   1370(1): 97-108 (Review)
Registered Authors
Alghisi, Elisa, Konantz, Martina, Lengerke, Claudia, North, Trista
Keywords
GPR56, Notch, endothelial-to-hematopoietic transition, hematopoiesis, hematopoietic stem cells
MeSH Terms
  • Animals
  • Cell Differentiation/physiology
  • Cell Lineage
  • Endothelial Cells/cytology*
  • Endothelial Cells/metabolism
  • Hematopoiesis/physiology
  • Hematopoietic Stem Cells/cytology*
  • Hematopoietic Stem Cells/metabolism
  • Humans
  • Receptors, Notch/metabolism*
  • Signal Transduction/physiology*
  • Zebrafish
  • Zebrafish Proteins/metabolism
PubMed
27015586 Full text @ Ann N Y Acad Sci
Abstract
During development, hematopoietic stem cells (HSCs) are formed in a temporally and spatially restricted manner, arising from specialized endothelial cells (ECs) in the ventral wall of the dorsal aorta within the evolutionary conserved aorta-gonad-mesonephros region. Our understanding of the processes regulating the birth of HSCs from ECs has been recently advanced by comprehensive molecular analyses of developing murine hematopoietic cell populations complemented by studies in the zebrafish model, with the latter offering unique advantages for genetic studies and direct in vivo visualization of HSC emergence. Here, we provide a concise review of the current knowledge and recent advances regarding the cellular origin and molecular regulation of HSC development, with particular focus on the process of endothelial-to-hematopoietic transition and its primary regulator, the Notch signaling pathway.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping