The kinetics of blood and organ engraftment following transplants of d
efined populations of hematopoietic stem/progenitor cells were investi
gated utilizing cell populations defined by surface antigen and rhodam
ine-123 staining, While long-term repopulating stem cells, short-term
multipotent progenitors and committed progenitors all reconstituted pe
ripheral blood red cells and splenic cellularity, only the population
of cells that includes highly enriched long-term repopulating stem cel
ls (Thy-1.1(low)Lin(neg)Sca-1(+)Rh123(low)) reconstituted marrow cellu
larity. In addition, peripheral blood platelet and nucleated cell coun
t increased only after transplant of the long-term repopulating popula
tion. These results argue that the major cell population that function
s to reconstitute hematopoiesis after bone marrow transplantation is a
primitive, marrow-homing stem cell, Transplantation of highly enriche
d multipotent progenitors that lack long-term reconstituting potential
had no impact on hematopoietic recovery, apart from a transient incre
ase in circulating erythrocytes. These results suggest that the primar
y cell population that functions to reconstitute hematopoiesis in a tr
ansplant setting is the long-term repopulating stem cell. This observa
tion is discussed in the contest of the normal hematopoietic process.