Flk-2 is a marker in hematopoietic stem cell differentiation: A simple method to isolate long-term stem cells

Clonogenic multipotent mouse hematopoietic stem cells (HSCs) and progenitor cells are contained within the c-kit(+) (K) lineage(-/lo) (L) Sca-1(+) (S) population of hematopoietic cells; long-term (LT) and short-term (ST) HSCs are Thy-1.1(lo). c-kit is a member of the receptor tyrosine kinase family, a class of receptors that are important in the proliferation and different iation of hematopoietic cells. To establish whether the Flk-2/'Flt3 recepto r tyrosine kinase was expressed on the most primitive LT-HSCs, we sorted hi ghly purified multipotent stem and progenitor cells on the basis of Flk-2 s urface expression and used them in competitive reconstitution assays. Low n umbers of Flk-2(-) HSCs gave rise to long-term multilineage reconstitution in the majority of recipients, whereas the transfer of Flk-2(+) multipotent cells resulted in mostly short-term multilineage reconstitution. The KLS s ubset of adult mouse bone marrow was analyzed for Flk-2 and Thy-1.1 express ion. Three phenotypically and functionally distinct populations were isolat ed: Thy(lo) Flk-2(LT-HSCs), Thy(lo) Flk-2(+) (ST-HSCs), and Thy(-) Flk-2(+) multipotent progenitors. The loss of Thy-1.1 and gain of Flk-2 expression marks the loss of self-renewal in HSC maturation. The addition of Flk-2 ant ibody to the lineage mix allows direct isolation of LT-HSC from adult bone marrow as c-kit(+) lin(-) Sca-1+ Flk-2- from many strains of mice. Fetal li ver HSCs are contained within Flk-2(-) and Flk-2(+) KTLS cells.