Table 1.

Extended growth of AML 1-ETO-expressing cells


Culture

Source

Weeks of proliferation

Growth medium
AE.1   CB   25   ML  
AE.2   CB   22   ML  
AE.4   PBPC   20   ML  
AE.5   CB   17   ML  
AE.6.3   PBPC   25   ML  
AE.6.5   PBPC   17   ML  
AE.6.8   PBPC   17   ML  
AE.6.9   PBPC   17   ML  
AE.6.10   PBPC   17   ML  
AE.6.11   PBPC   17   ML  
AE.6.12   PBPC   20   ML  
AE.9   CB   30   ML and SF  
AE.11   CB   32   ML and SF  
AE.11.1   CB   29   ML  
AE.11.2   CB   22   ML  
AE.11.3   CB   21   SF  
AE.11.4   CB   23   SF  
AE.11.5
 
CB
 
21
 
SF
 

Culture

Source

Weeks of proliferation

Growth medium
AE.1   CB   25   ML  
AE.2   CB   22   ML  
AE.4   PBPC   20   ML  
AE.5   CB   17   ML  
AE.6.3   PBPC   25   ML  
AE.6.5   PBPC   17   ML  
AE.6.8   PBPC   17   ML  
AE.6.9   PBPC   17   ML  
AE.6.10   PBPC   17   ML  
AE.6.11   PBPC   17   ML  
AE.6.12   PBPC   20   ML  
AE.9   CB   30   ML and SF  
AE.11   CB   32   ML and SF  
AE.11.1   CB   29   ML  
AE.11.2   CB   22   ML  
AE.11.3   CB   21   SF  
AE.11.4   CB   23   SF  
AE.11.5
 
CB
 
21
 
SF
 

Summary of 7 independent experiments, performed essentially as described in Figure 1. Growth media consisted of IMDM with 20% FBS and 7 cytokines (ML) or 5 cytokines in a serum-free media (SF). Experiments 6 and 11 (using PBPCs or cord blood [CB], respectively) involved splitting cultures into subcultures.

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