Table 4.

Epo, SCF, and Dex in the regulation of the erythroid gene expression program



Down-regulation

Up-regulation

Fold change less than -2
Fold change -2.0 to -1.75
Fold change -1.75 to -1.50
Fold change 1.50 to 1.75
Fold change 1.75 to 2.0
Fold change 2.0 to 2.5
Fold change more than 2.5
Epo, ‰ 0.9 4.8 10.2 12.7 4.2 1.8 1.2 
Dex, ‰   0.2   1.1   3.6   1.8   0.9   0.4   0.1  
SCF, ‰ 1.2 3.9 8.9 14.1 4.1 2.1 1.1 
Ratio ESD/ESZK, ‰
 
0.2
 
1.2
 
4.1
 
5.9
 
1.8
 
0.8
 
0.3
 


Down-regulation

Up-regulation

Fold change less than -2
Fold change -2.0 to -1.75
Fold change -1.75 to -1.50
Fold change 1.50 to 1.75
Fold change 1.75 to 2.0
Fold change 2.0 to 2.5
Fold change more than 2.5
Epo, ‰ 0.9 4.8 10.2 12.7 4.2 1.8 1.2 
Dex, ‰   0.2   1.1   3.6   1.8   0.9   0.4   0.1  
SCF, ‰ 1.2 3.9 8.9 14.1 4.1 2.1 1.1 
Ratio ESD/ESZK, ‰
 
0.2
 
1.2
 
4.1
 
5.9
 
1.8
 
0.8
 
0.3
 

Erythroid progenitors were factor deprived and restimulated with Epo, Dex, SCF, Epo/SCF, Epo/SCF/Dex, or Epo/SCF/ZK. Cy5-labeled cDNA synthesized from mRNA of restimulated cells was hybridized in parallel with Cy3-labeled cDNA synthesized from factor-deprived cells to the hematopoietic and the 17K EST arrays. Values in table represent the fraction (given in permillage [‰]) of cDNAs present on the microarrays that shows a certain fold change of expression in stimulated versus unstimulated cells.

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