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. 1999 Aug 15;19(16):7077–7088. doi: 10.1523/JNEUROSCI.19-16-07077.1999

Table 1.

Clonal analysis of E16 cortical cells grown in FGF2 alone or with BMP2

FGF2 FGF2 + BMP2
Fate of individual cells: n = 663 n = 816
 Nonviable 276 (41.6) 378 (46.3)
 Single cells 252 (38) 252 (30.9)
  Neurons 224 (88.9) 240 (95.2)
 Clones containing 2–4 cells 39 (5.9) 36 (4.4)
  with neurons 26 (66.7) 32 (88.9)
 Clones containing >4 cells 96 (14.5) 150 (18.4)
  with neurons 9 (10.7) 109 (72.7)
  with neurons and OLs 41 (42.7) 0 (0)
  with OLs 37 (38.5) 0 (0)
  without neurons or OLs 9 (10.7) 41 (27.3)
Cellular composition within clones:
 2–4 Cell clones with neurons, % neurons 100 96.9
 >4 Cell clones with neurons, % neurons   3.6 ± 1.2 20.5 ± 3.4**
 >4 Cell clones with OLs, % OLs  16.4 ± 2.8 1-a
Viability within clones
 Average # of viable cells per >4 cell clone 102.9 ± 11.9 70.3 ± 10.8
 Average # of nonviable cells per >4 cell clone  14.4 ± 2.0 18.2 ± 2.0

Clonal analysis of E16 cortical cells grown in FGF2 alone or FGF2 plus 1 ng/ml BMP2. Fate of individual cells, Each absolute value is followed by a percentage in parentheses, which reflects the percentage of all cells in that particular category. Cellular composition within clones, Viability within clones, Each value represents the mean ± SEM. Neurons and oligodendroglia were identified by β tubulin III and O4 expression, respectively. Cells expressing the astrocytic marker GFAP were not included because they were never seen as single cells or in small clones and were present in <1% of clones of more than four cells.

F1-a

No clones containing oligodendroglia were seen with BMP2 treatment.

*p < 0.05; **p < 0.01.