AJP - Renal Ad Instruments
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Renal Physiol 295: F688-F697, 2008. First published July 16, 2008; doi:10.1152/ajprenal.00133.2008 Free Article
0363-6127/08 $8.00
This Article
Free upon publication Free Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
295/3/F688    most recent
00133.2008v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Web of Science (1)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sui, G.-P.
Right arrow Articles by Fry, C. H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sui, G.-P.
Right arrow Articles by Fry, C. H.

Modulation of bladder myofibroblast activity: implications for bladder function

Gui-Ping Sui,1 Changhao Wu,2 Alexander Roosen,1 Youko Ikeda,3 Anthony J. Kanai,3 and Christopher H. Fry1

1Institute of Urology and 2Department of Medicine, University College London, London, United Kingdom; and 3Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania

Submitted 13 March 2008 ; accepted in final form 10 July 2008

Bladder suburothelial myofibroblasts may modulate both sensory responses from the bladder wall and spontaneous activity. This study aimed to characterize further these cells in their response to exogenous agents implicated in mediating the above activity. Detrusor strips, with or without mucosa, and isolated suburothelial myofibroblasts were prepared from guinea pig bladders. Isometric tension, intracellular Ca2+, and membrane current were recorded. Cell pairs were formed by pushing two cells together. Tension, intracellular Ca2+, and membrane potential were also recorded from bladder sheets using normal or spinal cord-transected (SCT) rats. Spontaneous contractions were greater in detrusor strips with an intact mucosa and were augmented by 10 µM UTP. ATP, UTP, or reduced extracellular pH elicited Ca2+ transients and inward currents (Erev –30 mV) in isolated cells. Capsaicin (5–30 µM) reduced membrane current (37 ± 12% of control) with minor effects on Ca2+ transients: sodium nitroprusside reduced membrane currents (40 ± 21% of control). Cell pair formation, without an increase in cell capacitance, augmented ATP and pH responses (180 ± 58% of control) and reduced the threshold to ATP and acidosis. Glivec (20–50 µM) reversibly blocked the augmentation and also reduced spontaneous activity in bladder sheets from SCT, but not normal, rats. Glivec also disrupted the spread of Ca2+ waves in SCT sheets, generating patterns similar to normal bladders. Suburothelial myofibroblasts respond to exogenous agents implicated in modulating bladder sensory responses; responses augmented by physical intercellular contact. The action of glivec and its selective suppression of spontaneous activity in SCT rats identifies a possible pathway to attenuate bladder overactivity.

suburothelium; spontaneous activity; purinergic signaling



Address for reprint requests and other correspondence: C. H. Fry, Postgraduate Medical School, Faculty of Health and Medical Sciences, Univ. of Surrey, Guildford GU2 7WG, UK (e-mail: c.h.fry{at}surrey.ac.uk)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2008 by the American Physiological Society.