Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2093815 | Stem Cell Reports | 2014 | 16 Pages |
•A multipotency assay reveals eight hematopoietic lineages from a single cell•The first embryonic multipotent cells are defined as CD11A− KIT+ SCA-1+ (CD11A− KLS)•Transplanted CD11A− KLS cells give rise to robust hematopoiesis in newborn mice•The early yolk sac is implicated as the major source of CD11A− KLS cells
SummaryHematopoiesis in the embryo proceeds in a series of waves, with primitive erythroid-biased waves succeeded by definitive waves, within which the properties of hematopoietic stem cells (multilineage potential, self-renewal, and engraftability) gradually arise. Whereas self-renewal and engraftability have previously been examined in the embryo, multipotency has not been thoroughly addressed, especially at the single-cell level or within well-defined populations. To identify when and where clonal multilineage potential arises during embryogenesis, we developed a single-cell multipotency assay. We find that, during the initiation of definitive hematopoiesis in the embryo, a defined population of multipotent, engraftable progenitors emerges that is much more abundant within the yolk sac (YS) than the aorta-gonad-mesonephros (AGM) or fetal liver. These experiments indicate that multipotent cells appear in concert within both the YS and AGM and strongly implicate YS-derived progenitors as contributors to definitive hematopoiesis.