- Open Access
Endothelio-hematopoietic relationship: getting closer to the beginnings
© Gordon-Keylock and Medvinsky; licensee BioMed Central Ltd. 2011
- Received: 15 December 2011
- Accepted: 28 December 2011
- Published: 28 December 2011
The close association between hematopoietic and endothelial cells during embryonic development led to the proposal that they may originate from a common ancestor - the hemangioblast. Due to a lack of unique specific markers for in vivo cell fate tracking studies, evidence supporting this theory derives mainly from in vitro differentiation studies. Teixeira and colleagues describe a novel enhancer that drives specific eGFP expression in blood islands of the electroporated chick embryo, thereby presenting a tool potentially suitable for analysis of hemangioblast differentiation and development of blood islands.
See research article: http://www.biomedcentral.com/1471-213X/11/76
- Hematopoietic Cell
- Primitive Streak
- Dorsal Aorta
- Blood Island
- Hematopoietic Development
What experimental confirmation is there of the existence of the hemangioblast? Due to the relative simplicity of manipulations and the ability to track cell populations of interest, pluripotent embryonic stem (ES) cells became broadly used to model hematopoietic development in vitro. The first evidence pointing to the existence of the bipotent hemangioblast was obtained when mouse ES cell-derived progenitors were shown to be capable of producing in vitro 'blast' colonies (BL-CFC), comprising both hematopoietic and vascular endothelial cells, in response to growth factors [6, 7]. ES cell differentiation has been extensively used to model the stepwise transition of the bipotent hemangioblast to the blood and endothelial lineages, shedding light on surface markers expressed at each stage as well as genetic regulation of this process [4, 5, 8] (Figure 1A). During hematopoietic differentiation, mouse ES cells first generate the primitive streak mesoderm marked by brachyury expression, followed by quick upregulation of Flk1, which marks the formation of extraembryonic mesoderm and the onset of endothelial specification. A fraction of hematogenic endothelial cells subsequently generates CD41+ and CD45+ hematopoietic cells, which critically depends on the transcription factor Runx1. It is broadly accepted that ES cell hematopoietic differentiation replicates yolk sac hematopoiesis; however, both yolk sac and intraembryonic hematopoietic compartments are believed to originate through an endothelial-hematopoietic transition.
Due to limitations in embryonic material and technical approaches, including lack of unique markers, in vivo studies of the endothelial-hematopoietic relationship in the early embryo are less abundant. Paradoxically, yolk sac blood islands, which prompted the concept of the hemangioblast in the first place, were for a long time a source of controversy. Initial attempts to identify bipotent cells capable of generating both endothelial and hematopoietic cells failed in both chicken and mouse embryos. Only later was evidence presented that hemangioblasts are transient cells localized to the posterior primitive streak and that by the time of migration to the yolk sac, hematopoietic and endothelial lineages are already segregated  (Figure 1B). Interestingly, while in the mouse the blood island appears as a single belt-like structure encompassing the yolk sac , blood islands in the chick represent multiple more distinct clusters of cells. One of the most interesting observations made by Teixeira et al. using live imaging is that blood island formation in the chick yolk sac involves very dynamic aggregation and recruitment of GFP+ cells during migration from the primitive streak. Thus, despite the morphological appearance of blood islands as individual clones in the chick, their clonal origin seems to be unlikely, as was proposed for the mouse . However, distinct multiple blood islands and availability of genetic markers such as that described by Teixeira et al. make the chick embryo a highly attractive model for studying hemangioblast biology and mechanisms underlying the segregation of endothelial and blood lineages.
Although in vitro hematopoietic cells can be generated from the hemangioblast through a hematogenic endothelium intermediate, exact details of this process in vivo remain obscure. For example, how and where exactly in the embryo do hematopoietic cells transit through an endothelial stage? Do all hematopoietic cells pass through an endothelial stage during embryonic development? In addition, some data indicate that hemangioblasts can generate smooth muscle cells, whereas other reports argue against this [6–10]. The full potency of these cells awaits further elucidation.
The relationship between hematopoietic cells and the endothelium is not limited to yolk sac blood islands. It is broadly thought that the best morphological demonstration of blood cell production by the endothelium is displayed in the midgestational dorsal aorta, umbilical cord and vitelline vessels connecting the embryo proper with the placenta and the yolk sac  (Figure 1C). Hematopoietic cells emerging in intra-aortic clusters show distinct morphological features and express markers common to both endothelial and hematopoietic cells, suggesting they are in transition from the underlying endothelium toward a blood cell fate. Individual cells with early hematopoietic markers such as c-kit, CD41 and CD45 can be detected prior to cluster formation in the endothelial layer of the dorsal aorta. Analysis of cultured thick sections of the mouse aorta-gonad-mesonephros region, an area containing intra-aortic hematopietic clusters, have shown that individual cells within the endothelial layer of the dorsal aorta can leave it and migrate inside the aortic lumen . Interestingly, live imaging of zebrafish embryos showed that during an endothelial-hematopoietic transition, cells leave the endothelial lining of the dorsal aorta in the opposite direction to that observed in mouse, and move away from the lumen before entering circulation through the cardinal vein below [13, 14].
The importance of finding novel specific markers for hemangioblasts and hematogenic endothelium in higher vertebrates cannot be overestimated. Such specific markers can significantly enhance in vitro clonal analysis of endothelial-hematopoietic differentiation and facilitate our understanding of hematopoietic development in vivo. Now that a methodology for generating transgenic chickens has become available , it is likely that the availability of useful markers and the accessibility of chick embryos for live imaging will significantly increase the use of avian models and will boost research in this area.
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