spacer gif spacer gif spacer gif spacer gif 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.


Figure 8


Fig. 8. Gata2-deficient ENC complemented with Gata2 exhibit much more active cyclin D1 and cyclin D2 transcription, while Gata2 transient overexpression blocks the proliferation of mouse neuroblastoma cells. (A-D) Gata2–/– ENC were transfected either with pAdRSV-GATA2HA and pAdRSV-ßGal plasmids (A,C) or with pAdRSV-ßGal alone, then treated for X-Gal colouration and in situ hybridisation with cyclin D1 (A,B) or cyclin D2 (C,D) antisense RNA probes. (E-J) NB2a mouse neuroblastoma cells, either control (E-G) or transiently transfected with pAdRSV-GATA2HA (H-J). BrdU was added in the culture medium 30 hours after transfection, cells were recovered 15 hours later, processed for BrdU staining (F,I) and further HA-immunostained (I, red); nuclei were stained with DAPI (E,H) before mounting. (G,J) Superimpositions of E,F (G) and H,I (J). In the control culture (E-G), cells have not stopped growing and are all BrdU positive; whereas in transfected cultures (H-J), cells have not reached the same density and, especially GATA2-HA expressing cells, have not incorporated BrdU (J). Scale bar: 45 µm in A-D; 15 µm in E-J.





Right arrow Return to article