期刊名称：Proceedings of the National Academy of Sciences
印刷版ISSN：0027-8424
电子版ISSN：1091-6490
出版年度：2001
卷号：98
期号：25
页码：14541-14546
DOI：10.1073/pnas.261562798
语种：English
出版社：The National Academy of Sciences of the United States of America
摘要：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-1.1lo. c-kit is a member of the receptor tyrosine kinase family, a class of receptors that are important in the proliferation and differentiation of hematopoietic cells. To establish whether the Flk-2/Flt3 receptor tyrosine kinase was expressed on the most primitive LT-HSCs, we sorted highly purified multipotent stem and progenitor cells on the basis of Flk-2 surface expression and used them in competitive reconstitution assays. Low numbers 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 subset of adult mouse bone marrow was analyzed for Flk-2 and Thy-1.1 expression. Three phenotypically and functionally distinct populations were isolated: Thylo Flk-2- (LT-HSCs), Thylo 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 antibody 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 liver HSCs are contained within Flk-2- and Flk-2+ KTLS cells.
