Peripheral blood stem cells (PBSCs) were mobilized in mice by treatmen
t with cytosine-arabinoside on day 0, followed by the administration b
y injection of granulocyte colony-stimulating factor for 4 days. There
were remarkable increases in the numbers of cells with lineage-negati
ve (Lin(-)) c-kit(+) markers, cells with colony-forming unit-cell (CFU
-C) and colony-forming unit-spleen (CFU-S) activities, and cells with
marrow-repopulating ability (MRA) in the extramedullary sites (the spl
een, peripheral blood, and liver) on day 5, whereas the number of thes
e immature hematopoietic cells decreased in the bone marrow (PM) on da
y 5, This finding suggests the mobilization of immature hematopoietic
cells from the BM to the extramedullary sites, Three-color flow cytome
tric analyses showed that CD4 antigen was not expressed on the Lin(-)S
ca-1(+) cells in the mobilized PB cells (PBCs), although CD4(lo) cells
were found in those of normal BM cells, Lin(-)c-kit(+) cells in the m
obilized PBCs contained more cells with immature phenotypes (Sca-1(+)
Thy1.2(lo), CD71(-), and Rh123(dull)) than in normal BMCs, indicating
an alteration of the hierarchical composition of the Lin(-)c-kit(+) ce
lls, The Lin(-)c-kit(+)Sca-1(+) cells in the mobilized PBCs had simila
r CFU-C and CFU-S activities to those in normal BMCs, Electron microsc
opic studies of these cells in the mobilized PBCs showed that only 10%
to 20% of these cells had a thin rim of cytoplasm with poorly develop
ed organelles. Allogeneic transplantation [B6-->C3H] of PBSCs showed l
ong-term reconstituting activity across the major histocompatibility c
omplex barrier 24 weeks after transplantation, although longer observa
tion is necessary. (C) 1996 by The American Society of Hematology.