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Review
. 2013 Feb;1830(2):2395-403.
doi: 10.1016/j.bbagen.2012.10.004. Epub 2012 Oct 12.

The biochemistry of hematopoietic stem cell development

Affiliations
Review

The biochemistry of hematopoietic stem cell development

P Kaimakis et al. Biochim Biophys Acta. 2013 Feb.

Abstract

Background: The cornerstone of the adult hematopoietic system and clinical treatments for blood-related disease is the cohort of hematopoietic stem cells (HSC) that is harbored in the adult bone marrow microenvironment. Interestingly, this cohort of HSCs is generated only during a short window of developmental time. In mammalian embryos, hematopoietic progenitor and HSC generation occurs within several extra- and intraembryonic microenvironments, most notably from 'hemogenic' endothelial cells lining the major vasculature. HSCs are made through a remarkable transdifferentiation of endothelial cells to a hematopoietic fate that is long-lived and self-renewable. Recent studies are beginning to provide an understanding of the biochemical signaling pathways and transcription factors/complexes that promote their generation.

Scope of review: The focus of this review is on the biochemistry behind the generation of these potent long-lived self-renewing stem cells of the blood system. Both the intrinsic (master transcription factors) and extrinsic regulators (morphogens and growth factors) that affect the generation, maintenance and expansion of HSCs in the embryo will be discussed.

Major conclusions: The generation of HSCs is a stepwise process involving many developmental signaling pathways, morphogens and cytokines. Pivotal hematopoietic transcription factors are required for their generation. Interestingly, whereas these factors are necessary for HSC generation, their expression in adult bone marrow HSCs is oftentimes not required. Thus, the biochemistry and molecular regulation of HSC development in the embryo are overlapping, but differ significantly from the regulation of HSCs in the adult.

General significance: HSC numbers for clinical use are limiting, and despite much research into the molecular basis of HSC regulation in the adult bone marrow, no panel of growth factors, interleukins and/or morphogens has been found to sufficiently increase the number of these important stem cells. An understanding of the biochemistry of HSC generation in the developing embryo provides important new knowledge on how these complex stem cells are made, sustained and expanded in the embryo to give rise to the complete adult hematopoietic system, thus stimulating novel strategies for producing increased numbers of clinically useful HSCs. This article is part of a Special Issue entitled Biochemistry of Stem Cells.

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Figures

Figure 1
Figure 1
Hematopoietic stem cell development in the mouse embryo. A) Depiction of a mouse embryo at day 10.5 at the time when the first hematopoietic stem cells are generated in the aorta. Sites harboring (and/or generating) hematopoietic cells are shown: the extraembryonic yolk sac and placenta, the intraembryonic aorta and liver, and the umbilical and vitelline vessels that respectively connect the placenta and yolk sac to the aorta. The dotted line through the trunk of the embryo indicates the transverse section shown in panel B. B) Depiction of a transverse section through an E10.5 mouse embryo with the AGM (aorta-gonad-mesonephros/ aorta and urogenital ridges) region in the red rectangle. The AGM is flanked on the dorsal side by the neural tube and the somites, and on the ventral side by the gut and peritoneum. A hematopoietic cluster is indicated on the ventral wall of the dorsal aorta. Hematopoietic stem cells are localized in the clusters. C) A close up of the ventral wall of the aorta showing cluster formation. A hemogenic endothelial cell is undergoing the transition from endothelial cell to a hematopoietic cell.
Figure 2
Figure 2
De novo generation of hematopoietic cells begins shortly after mesoderm formation and continues through mouse midgestation. Extrinsic factors that include morphogens such as FGF, Hh and BMPs produced in surrounding microenvironment affect mesodermal cells in hematopoietic fate choice and differentiation. These signaling pathways, as well as the Notch and VEGF pathways, impact directly or indirectly on the expression of several hematopoietic transcription factors in the presumptive hematopoietic cells in different hematopoietic sites and stages of development. The transcription factors directing hematopoietic fate and blood cell production include SCL, Gata2 and Runx1, amongst others. The specific temporal and spatial sequence of extrinsic signals, the combination and/or the levels of extrinsic signals play a role in the differential transcription factor expression and production of the distinct waves of hematopoietic cells in the developing embryo.

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