Table 1

Expansion of MSCs in culture

Days in cultureDonor 1, ×1000 cells/cm2Donor 3, ×1000 cells/cm2Donor 4, ×1000 cells/cm2Donor 5, ×1000 cells/cm2
3.4 ± 0.5 3.6 ± 1.1 4.6 ± 0.6 6.2 ± 0.5* 
6.4 ± 0.8 5.7 ± 0.5 10.3 ± 1.6 15.1 ± 2.1 
15.6 ± 2.2 16.2 ± 3.6 20.1 ± 1.6 30.2 ± 7.9 
30.5 ± 5.6 > 19.0 > 42.0 42.9 ± 5.7 
> 50.0 > 26.0 > 52.0 > 57.0 
Days in cultureDonor 1, ×1000 cells/cm2Donor 3, ×1000 cells/cm2Donor 4, ×1000 cells/cm2Donor 5, ×1000 cells/cm2
3.4 ± 0.5 3.6 ± 1.1 4.6 ± 0.6 6.2 ± 0.5* 
6.4 ± 0.8 5.7 ± 0.5 10.3 ± 1.6 15.1 ± 2.1 
15.6 ± 2.2 16.2 ± 3.6 20.1 ± 1.6 30.2 ± 7.9 
30.5 ± 5.6 > 19.0 > 42.0 42.9 ± 5.7 
> 50.0 > 26.0 > 52.0 > 57.0 

Frozen vials containing approximately 106 passage 1 MSCs from 5 donors were thawed, plated in 174-cm2 dishes, incubated for 1 day, replated at 100 cells/cm2 on the next day, and cultured for 5 to 9 days. Confluency was estimated by phase microscopy of the cultures and cell density by counting with a hemocytometer of cultures lifted with trypsin/EDTA.

EDTA indicates ethylenediaminetetraacetic acid; and MSC, multipotent stromal cells.

*

Values are mean plus or minus SD (n = 5).

Cells aggregated.

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