Table 3.

In vivo labeling kinetics of CD34+ cells during [2H2]-glucose infusion


Donor ID

% newly produced cells, “f” × 100*

Fractional replacement rates, klabeling/d*

Replacement t1/2labeling, d*

Replacement t1/2delabeling, d
D06   45.8   0.312   2.2   6.2  
D08   50.1   0.617   1.4   9.2  
D10   40.7   0.405   1.7   3.8  
D16   40.6   0.264   2.6   3.0  
D20   29.2   0.182   3.8   ND  
D21   28.5   0.168   4.1   ND  
D22
 
41.1
 
0.281
 
2.5
 
ND
 

Donor ID

% newly produced cells, “f” × 100*

Fractional replacement rates, klabeling/d*

Replacement t1/2labeling, d*

Replacement t1/2delabeling, d
D06   45.8   0.312   2.2   6.2  
D08   50.1   0.617   1.4   9.2  
D10   40.7   0.405   1.7   3.8  
D16   40.6   0.264   2.6   3.0  
D20   29.2   0.182   3.8   ND  
D21   28.5   0.168   4.1   ND  
D22
 
41.1
 
0.281
 
2.5
 
ND
 

Marrow aspirates were obtained within 2 hours (day 0) after the end of the continuous [2H2]-glucose infusion period. CD34+ cells were selected from low-density marrow cells and processed as described in “Patients, materials, and methods”. ND indicates not determined.

*

Values were calculated as described in “Patients, materials, and methods” and calculations for % newly produced cells (that is, one new cell added per cell division) take into consideration the mean plasma glucose enrichment. Calculations for fractional replacement rates (klabeling/day) and replacement rate t1/2labeling also take into account the number of hours of continuous [2H2]-glucose infusion.

Replacement t1/2delabeling values were estimated from the decrease in %[2H2] dA enrichment observed at week 2. Estimates of t1/2delabeling determined from the decrease [2H2] dA enrichment between week 2 and week 4 were 82 days (D08) and 17.2 days (D10) and 6 to 7 days for 3 other donors who did not have day 0 marrows evaluated.

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