spacer gif spacer gif spacer gif spacer gif ARCHIVE ANNOUNCEMENT! spacer gif
 QUICK SEARCH:   [advanced]


spacer gif
     Home     Help     Feedback     Subscriptions     Archive     Search     Table of Contents    


Right arrow Help viewing high resolution images
Right arrow Return to article
(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. 4. Dorsal-to-ventral migration within the basal telencephalon. (A) A grafting experiment performed at E13.5, in which ventrally migrating cells are analysed. The box delineates the area shown in C-E''. (B) Example of a graft in which GFP-positive cells have reached the POa. Arrows in C show co-localization of COUP-TFI (red) with GFP (green), whereas no co-labelling with COUP-TFII (red) has been identified (D) within the migratory cells. (E-E'') Arrows in (E'') indicate that migrating cells are neurons by double labelling of GFP (green) with Tuj1 (red). (E'') is a merge of panels (E) and (E'). (F) Double immunofluorescence of COUP-TFI (green) and GABA (red) shows that some COUP-TFI-positive cells (arrows) are GABAergic in the ventral migratory stream. (G) By electroporation of a GFP-expressing construct into the MLGE region, GFP-positive cells migrate ventrally, and these cells express COUP-TFI (arrows in H). Similarly, by inserting a DiI crystal into the MLGE region, fluorescent cells are detected ventrally, in the POa/hypothalamic region (I). These cells co-express COUP-TFI (J). The arrow indicates a leading process. Note that the diffuse red signal in J is the result of the DiI signal after fixation.





Right arrow Return to article