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Blood, 1 January 2008, Vol. 111, No. 1, pp. 4-5.
A photographic fishing expedition with granieMORGAN STANLEY CHILDREN'S HOSPITAL OF NEWYORK-PRESBYTERIAN, COLUMBIA UNIVERSITY
In this issue of Blood, Le Guyader and colleagues use a variety of elegant techniques during zebrafish development to identify a unique population of neutrophils derived from myeloid progenitors originating from primitive embryonic macrophages.
Hematopoiesis was originally thought to arise only from the intermediate cell mass (ICM) or caudal hematopoietic tissue (CHT) located in the posterior region between the notochord endoderm in primitive zebrafish. However, researchers have recently identified a second site of embryonic "primitive" hematopoiesis that originates in the anterior-lateral mesoderm (rostral blood island [RBI]) and eventually migrates to the kidney, which serves as the location of "definitive" hematopoiesis during the remainder of the zebrafish's development and lifespan.1,2 In contrast, in mammals, primitive hematopoiesis originates from mesoderm outside the embryo that migrates onto the embryonic yolk sac to develop blood islands; during the course of further development, it migrates to the aorta-gonad-mesonephros (AGM) region, fetal liver, and finally the bone marrow for "definitive" hematopoiesis.1–3 Macrophages have been identified as the first leukocytes to be derived during developmental myelopoiesis in vertebrate embryos, originate from the RBI, before dispersing throughout the embryonic mesenchyme prior to blood circulation in the developing zebrafish. Neutrophilic granulocytes appear next in primitive hematopoiesis and are identified in blood circulation and connective tissue (mesenchyme) by 48 hours after fertilization (hpf). Neutrophil development during mammalian hematopoiesis was thought to originate from primitive hematopoietic cells similar to macrophages but not from macrophages themselves. In this issue, Le Guyader and coworkers have identified a unique subset of neutrophilic granulocytes that originate from primitive macrophages from the RBI giving rise to precursor primitive myeloid progenitor cells. Furthermore, these neutrophilic granulocytes arising from primitive macrophages have unique properties, including expression of PU.1 and L-plastin, migrating toward invading microbes without phagocytosis, and are dispersed into mesenchyme and epidermis but not the blood circulation. Using a fluorescein dye to detect peroxidase activity of activated granulocytes by an ultraviolet laser, Le Guyader et al show, through cell tracing of sudan black (SB)–stained granulocytes, a population of neutrophilic granulocytes that were derived from myeloid progenitors originating from primitive macrophages of the RBI (see figure).
These novel findings of a unique population of neutrophils derived from primitive macrophages are contrary to the dogma of mammalian myelopoiesis and provide direction for future critical investigations. Does this unique population exist in the human neonate, providing a partial source for their immaturity in phagocytic immunity?4 What are the molecular mechanisms regulating this developmental process, and can they be exploited for ex vivo human myelopoiesis? What, if any, is the role of this population of neutrophils in tissue injury, repair, and defense in humans? Le Guyader et al have shed a new light on the origin and regulation of developmental vertebrate myelopoiesis.
Footnotes
Conflict-of-interest disclosure: The author declares no competing financial interests.
REFERENCES
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| Copyright © 2008 by American Society of Hematology Online ISSN: 1528-0020 | |||||||||
