Table 1.

Effects of Oligonucleotides on CFU-GM Staining for Unspecific Esterase

Additive Positive Mixed Positive Mixed NegativeNegative
Oligo buffer  3 ± 0.6  39 ± 4 23 ± 2  33 ± 6  
AS1 2.5 μmol/L  0 ± 0.0 20 ± 4  40 ± 4  44 ± 6  
AS1 5.0 μmol/L 0 ± 0.0  20 ± 1  31 ± 6  48 ± 5  
AS1 10.0 μmol/L  0 ± 0.0  26 ± 1  26 ± 5 47 ± 6  
CO 2.5 μmol/L  2 ± 0.5  44 ± 2 19 ± 2  44 ± 6  
CO 5.0 μmol/L  0 ± 0.0 49 ± 3  22 ± 3  33 ± 3  
CO 10.0 μmol/L 3 ± 0.7  48 ± 2  19 ± 1  30 ± 2 
Additive Positive Mixed Positive Mixed NegativeNegative
Oligo buffer  3 ± 0.6  39 ± 4 23 ± 2  33 ± 6  
AS1 2.5 μmol/L  0 ± 0.0 20 ± 4  40 ± 4  44 ± 6  
AS1 5.0 μmol/L 0 ± 0.0  20 ± 1  31 ± 6  48 ± 5  
AS1 10.0 μmol/L  0 ± 0.0  26 ± 1  26 ± 5 47 ± 6  
CO 2.5 μmol/L  2 ± 0.5  44 ± 2 19 ± 2  44 ± 6  
CO 5.0 μmol/L  0 ± 0.0 49 ± 3  22 ± 3  33 ± 3  
CO 10.0 μmol/L 3 ± 0.7  48 ± 2  19 ± 1  30 ± 2 

Mononuclear bone marrow cells were obtained by gradient centrifugation and cultured in agar for 14 days. At days 0 and 7, antisense RB oligonucleotides (AS1) or control oligonucleotides (CO), respectively, were added at the indicated concentrations. At day 14, agar dishes were fixated and stained for unspecific esterase as a marker of monocytic differentiation. A colony (>40 cells) was defined as positive if all of its cells stained and mixed positive if a majority but not all of its cells stained. A colony was defined as negative if none of its cells stained and mixed negative if a minority of its cells stained. Values shown are percentages of colonies. Results shown represent the mean values from 3 separate experiments ± SEM.

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