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.



Fig. 2. p63–/– prostate lacks basal cells. Both p63+/+ (A) and p63–/– (B) urogenital sinus (UGS) formed prostate when grafted into intact male hosts. When p63–/– UGS was grafted into castrated male hosts, the UGS developed into a large cyst without ducts (C). The prostatic ducts were surrounded by smooth muscle cells expressing smooth muscle actin (SMA) (D,E). Morphologically definable basal cells (black arrow in F,H) were not observed in p63–/– prostate (G,I). p63–/– prostate contained goblet cells (G,I, white arrows) (see also Fig. 3). Elongated/flat nuclei of stromal cells should not be confused with basal cells. Expression of basal cell markers was examined in p63+/+ (J,L,N,P) and p63–/– (K,M,O,Q) prostates. p63 (J,K), K14 (L,M), transglutaminase II (TGII,N,O) and maspin (P,Q) were detected only in p63+/+ prostate. All basal cell markers were absent in p63–/– prostate (K,M,O,Q). RT-PCR for K14 (R) confirmed results of IHC. K14 mRNA was detected in host prostate (coagulating gland + ventral prostate + dorsolateral prostate, lane 1) and three p63+/+ prostatic grafts (lanes 2-4) but not in p63–/– prostates (lanes 5 and 6). ß-actin was used for control.





Right arrow Return to article