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. 2005 Nov 8;107(5):2180–2183. doi: 10.1182/blood-2005-05-1922

Table 1.

Chimerism in primary sheep that received transplants of hESC-derived HSCs

Chimerism in BM by PCR, %*(time, mo)
Chimerism by FACS, % (time, mo)
Animal no. No. H1 passages Cell type No. cells BM PB
1748 56 CD34+/Lin- 140 000 0.05 (39) 0.1 (10) 0.1 (10)
1749 56 CD34+/Lin- 140 000 0 (39) 0.1 (10) 0.1 (10)
1757 56 CD34+/Lin- 100 000 + (6) 0 (5) 0.1 (5)
1838 35 CD34+/CD38- 95 000 0.04 (35) 0 (7) 0 (7)
1871 45 CD34+/CD38- 26 500 0 (34) 0 (6) 0 (6)
1885 48 CD34+/CD38- 63 000 0.09 (33) 0.1 (17) 0.2 (17)
1886 49 CD34+/CD38- 70 000 0.001 (33) 0.1 (17) 0.1 (17)
1887 49 CD34+/CD38- 70 000 0.001 (33) 0 (17) 0.1 (17)

FACS indicates fluorescence-activated cell sorter.

*

Real-time quantitative PCR was carried out for human microsatellite DNA (Supplemental Methods) on BM samples at various periods after transplantation. PCR data for PB samples at the matching time points were all negative. Analyses were repeated at least once to confirm data reported. Minimal detection limit = 0.0001%

Flow cytometry analyses for human CD34 or CD45 was carried out at various periods after transplantation. Twenty thousand to 50 000 events were acquired for a single analysis per animal at the noted time point

Animal no. 1757 was analyzed by PCR for human GAPDH (Figure S1)