Table 1.

Epitope profile of CR cells and BM cells




CR cells

BM cells
CD10   21 ± 23   9.9 ± 10  
CD31   0.8 ± 0.5   0.6 ± 0.3  
CD34   0.6 ± 0.2   0.4 ± 0.5  
CD44   93 ± 5.4   74 ± 30  
CD45   0.6 ± 0.4   0.7 ± 0.5  
CD54*  48 ± 2.0   15 ± 9.8  
CD90   99 ± 1.0   92 ± 13  
CD105   95 ± 6.0   74 ± 41  
CD106*  50 ± 21   15 ± 3.9  
CD117   0.8 ± 0.1   0.7 ± 0.3  
CD147   99 ± 1.0   95 ± 6.7  
CD166   74 ± 32   68 ± 45  
Flk-1   1.3 ± 0.4   1.2 ± 0.4  
NGFR
 
14 ± 19
 
6.9 ± 7.6
 



CR cells

BM cells
CD10   21 ± 23   9.9 ± 10  
CD31   0.8 ± 0.5   0.6 ± 0.3  
CD34   0.6 ± 0.2   0.4 ± 0.5  
CD44   93 ± 5.4   74 ± 30  
CD45   0.6 ± 0.4   0.7 ± 0.5  
CD54*  48 ± 2.0   15 ± 9.8  
CD90   99 ± 1.0   92 ± 13  
CD105   95 ± 6.0   74 ± 41  
CD106*  50 ± 21   15 ± 3.9  
CD117   0.8 ± 0.1   0.7 ± 0.3  
CD147   99 ± 1.0   95 ± 6.7  
CD166   74 ± 32   68 ± 45  
Flk-1   1.3 ± 0.4   1.2 ± 0.4  
NGFR
 
14 ± 19
 
6.9 ± 7.6
 

The CR cells and BM cells at Passage 0 were harvested 14 days after plating and labeled with antibodies against human antigens CD10, CD31, CD34, CD44, CD45, CD54 (ICAM-1), CD90 (Thy-1), CD105 (endogrin, SH2), CD117 (c-kit), CD147, CD166 (ALCAM, SB-10), Flk-1 (VEGF receptor 2), and NGFR (nerve growth factor receptor) and analyzed by flow cytometry. Positive expression was defined as the level of fluorescence greater than 99% of the corresponding isotype-matched control antibodies. All analyses were performed on 5 donors. Positive expression rates (%) are displayed as mean ± SD.

*

CR cells had a higher expression than the BM cells for CD54 and CD106 (P < .05; 2-factor ANOVA).

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