(Downloading may take up to 30 seconds.
If the slide opens in your browser, select File -> Save As to save it.)

Click on image to view larger version.



Fig. 1. Immunomicrograph showing the CNS potential of E14 rat dorsal spinal cord-derived clones. (A) A single clone can generate ß-tubulin+ neurones, O4+ oligodendrocytes and GFAP+ astrocytes. (B) Hedgehog signalling is not necessary for the generation of oligodendrocytes from FGF2-treated E14 rat dorsal cultures. Addition of cyclopamine or KAAD during the 7 day exposure to FGF2 does not significantly reduce numbers of oligodendrocytes generated upon mitogen withdrawal, plating and subsequent differentiation for a further 7 days (P>0.05). (C) Immunofluorescent micrograph showing representative labelling of differentiating cultures for O4-, GC- and MBP-positive cells from E14 dorsal-derived cultures following treatment with FGF2 in the presence of cyclopamine (1 µM).