Table 1.

Origin of hematopoietic cells and CFU-S12 in ossicle marrow

OssicleOrigin of marrow cells from renal ossicles
Hematopoietic cellsCFU-S12population
Donor (Ly-5.1)Host (Ly-5.1+)Donor
(zfy-1/neo+)
Host
(zfy-1+/neo)
Endogenous
(zfy-1/neo/M-CSF+)
77d-N2 3.5% 96.5% 19/28 (67.86%) 9/28 (32.14%) 0/28 
133d-N1 ND ND 14/15 (93.33%) 1/15 (6.67%) 0/15 
136d-N1 30.4% 69.6% 61/74 (83.56%) 12/74 (16.44%) 1/74 
281d-N2 16.4% 83.4% 4/27 (16%) 21/27 (84%) 2/27 
OssicleOrigin of marrow cells from renal ossicles
Hematopoietic cellsCFU-S12population
Donor (Ly-5.1)Host (Ly-5.1+)Donor
(zfy-1/neo+)
Host
(zfy-1+/neo)
Endogenous
(zfy-1/neo/M-CSF+)
77d-N2 3.5% 96.5% 19/28 (67.86%) 9/28 (32.14%) 0/28 
133d-N1 ND ND 14/15 (93.33%) 1/15 (6.67%) 0/15 
136d-N1 30.4% 69.6% 61/74 (83.56%) 12/74 (16.44%) 1/74 
281d-N2 16.4% 83.4% 4/27 (16%) 21/27 (84%) 2/27 

The contribution of BM-donor–derived (Ly-5.1) and ossicle-host–derived (Ly-5.1+) hematopoietic cells was quantified in the bulk of the ossicle marrow by flow cytometry. The origin of the CFU-S12 population was determined on individually excised colonies by DNA hybridization with aneor gene probe (1200-bp EcoRI/SalI fragment from pXT1 plasmid DNA)15 and a male probe from thezfy-1 gene (1400-bp EcoRI/SalI fragment from pY2 plasmid).16 A probe for the single copy M-CSFgene (1100-bp EcoRI/HindIII fragment of plasmid pSPmM1)17was used as a DNA load control. Data are presented as the ratio of colonies of the respective origin versus the total number of CFU-S12 analyzed per ossicle. The percentage of donor and host-derived colonies with respect to the total number of exogenous colonies is shown in brackets.

CFU-S indicates spleen colony-forming unit; ND, not determined.

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