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Hematopoietic stem cell‐independent hematopoiesis: emergence of erythroid, megakaryocyte, and myeloid potential in the mammalian embryo
Author(s) -
Palis James
Publication year - 2016
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1002/1873-3468.12459
Subject(s) - yolk sac , haematopoiesis , biology , megakaryocyte , progenitor cell , microbiology and biotechnology , stem cell , hemangioblast , myeloid , embryonic stem cell , immunology , blood cell , embryo , genetics , gene
Steady‐state production of all circulating blood cells in the adult ultimately depends on hematopoietic stem cells ( HSC s), which first arise in small numbers beginning at embryonic day (E) 10.5 in large arterial vessels of the murine embryo. However, blood cell synthesis first begins in the yolk sac beginning at E7.25 and consists of two waves of hematopoietic progenitors. The first wave consists of primitive erythroid, megakaryocyte, and macrophage progenitors that rapidly give rise to maturing blood cells of all three lineages. This ‘primitive’ wave of progenitors is followed by a partially overlapping wave of ‘erythro‐myeloid progenitors’, which contain definitive erythroid, megakaryocyte, macrophage, neutrophil, and mast cell progenitors that seed the fetal liver and jump‐start hematopoiesis before the engraftment and expansion of HSC s. These two waves of progenitors that arise in the yolk sac are necessary and even sufficient to sustain the survival of the mouse embryo until birth in the absence of HSC s. They provide key signals to support HSC emergence. Finally, HSC ‐independent hematopoiesis also provides long‐lived tissue‐resident macrophage populations that function in multiple adult organs.