Table 1.

Contribution of Notch1-deficient and wild-type cells to definitive hematopoiesis in chimeric mice


Chimera age

Organ assayed

Notch1 genotype

No. of chimeras analyzed

No. of different ES lines

Percent LacZ+ CFU

Range
9.5 to 10.5   YS   +/+   1   1   29   
   -/-   6   3   35 ± 19   15-66  
11.5 to 12.5   YS   +/+   1   1   33   
   -/-   8   2   4 ± 5   0-14  
13.5 to 14.5   FL   +/+   1   1   51   
   -/-   2   1   4.5   4-5  
15.5 to postnatal   FL/BM   +/+   5   2   40 ± 17   25-68  

 

 
-/-
 
10
 
3
 
0
 
0
 

Chimera age

Organ assayed

Notch1 genotype

No. of chimeras analyzed

No. of different ES lines

Percent LacZ+ CFU

Range
9.5 to 10.5   YS   +/+   1   1   29   
   -/-   6   3   35 ± 19   15-66  
11.5 to 12.5   YS   +/+   1   1   33   
   -/-   8   2   4 ± 5   0-14  
13.5 to 14.5   FL   +/+   1   1   51   
   -/-   2   1   4.5   4-5  
15.5 to postnatal   FL/BM   +/+   5   2   40 ± 17   25-68  

 

 
-/-
 
10
 
3
 
0
 
0
 

Contribution of Notch1-deficient (Notch1Δ1 allele) ES cells (-/-) and control wild-type (+/+) ES cells to definitive hematopoietic CFU progenitors in yolk sac (YS), fetal liver (FL), and bone marrow (BM) of high-percentage chimeras at various stages of development. Colonies were stained with X-gal stain to determine the percentages of overall colonies obtained from ES-derived (LacZ+) and embryo-derived (LacZ-) progenitors. We did not observe any bias in the distribution of erythroid, myeloid (macrophage or monocyte/granulocyte), or mixed colonies in the LacZ+ and LacZ- populations (not shown). For each age range, the number of chimera analyzed and the number of different ES lines used to generate these chimeras are indicated, as well as the average, standard deviation, and range of percent contribution of LacZ+ CFUs.

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