Table 2.
Plating efficiency (%) | Types of colonies (%) | |||
---|---|---|---|---|
All neurons | Some neurons | No neurons | ||
No add | ||||
20% O2 | 22.7 ± 8.5 | 0.0 ± 0.0 | 0.0 ± 0.0 | 100.0 ± 0.0 |
∼5% O2 | 33.4 ± 7.3* | 0.0 ± 0.0 | 0.4 ± 0.9 | 99.6 ± 0.9 |
+BMP2 | ||||
20% O2 | 26.8 ± 8.9 | 31.5 ± 17.9 | 52.5 ± 18.9 | 15.9 ± 5.7 |
∼5% O2 | 43.4 ± 11.5* | 59.5 ± 10.8* | 35.0 ± 11.1 | 5.5 ± 1.4* |
p75+P0− cells were sorted into cultures at clonal density and cultured for 5 or 6 d, followed by staining for peripherin, a marker of peripheral neurons. Plating efficiency indicates the percentage of cells initially sorted into culture that went on to form colonies. Data are presented as mean ± SD for five independent experiments. Results at different oxygen concentrations (within no add or +BMP2 treatments) were compared byt tests, and significantly different statistics are noted by asterisks (p < 0.05). Decreased oxygen culture significantly increased plating efficiency in both treatments and neuronal differentiation in the presence of BMP2.