AJP - GI Email Content Delivery
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Gastrointest Liver Physiol 292: G1403-G1410, 2007; doi:10.1152/ajpgi.00478.2005
Right arrow Help viewing high resolution images
Right arrow Return to article
pripka{at}the-aps.org

(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 6


Fig. 6. Disruption of subapical F-actin is unaffected by 8-Br-cAMP or Epac. A and D: pancreatic acini were stimulated with either carbachol or caerulein with or without 8-Br-cAMP (100 µM) or the Epac agonist 8-pCPT-2'-O-Me-cAMP (100 µM). Cells were fixed and stained with rhodamine-phalloidin (red) for F-actin and TOPRO-3 (blue) for nuclei. Representative images from 3 independent experiments are shown. B and E: apical intensities were measured for each sample and expressed relative to unstimulated cells. C and F: ratio of fluorescence intensities of the apical to basolateral regions were determined for each condition. Unstim., unstimulated; Carb, carbachol. Seven cells were analyzed per condition and expressed as means ± SE. *,#,{blacklozenge}P < 0.05 for either carbachol (1 mM) alone, with 8-Br-cAMP, or with 8-pCPT-2'-O-Me-cAMP compared with unstimulated, respectively.





Right arrow Return to article


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2007 by the American Physiological Society.