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


     


This Article
Right arrow Full Text Free
Right arrow Full Text (PDF) Free
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kuc, R. E.
Right arrow Articles by Davenport, A. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kuc, R. E.
Right arrow Articles by Davenport, A. P.
Experimental Biology and Medicine 231:741-745 (2006)
© 2006 Society for Experimental Biology and Medicine


BASIC BIOLOGY

Quantification of Endothelin Receptor Subtypes in Peripheral Tissues Reveals Downregulation of ETA Receptors in ETB-Deficient Mice

Rhoda E. Kuc1, Janet J. Maguire and Anthony P. Davenport

Clinical Pharmacology Unit, University of Cambridge, Level 6, Addenbrooke’s Centre for Clinical Investigation, Addenbrooke’s Hospital, Cambridge CB2 2QQ, United Kingdom

To whom requests for reprints should be addressed at 1 Clinical Pharmacology Unit, University of Cambridge, Level 6, Addenbrooke’s Centre for Clinical Investigation, Box 110, Addenbrooke’s Hospital, Cambridge CB2 2QQ, UK. E-mail: rek22{at}medschl.cam.ac.uk

Abstract

We have previously shown that in homozygous endothelin (ET)B /– deficient mice, ETA receptor density is significantly downregulated in the brain by 45%. In these mice, plasma ET-1 levels are elevated. Our aim was to use quantitative autoradiography to establish the distribution of ET receptor subtypes in peripheral tissues from wild-type mice and to measure the density of the ETA subtype in ETB– /– knockout animals. Our second aim was to test whether deletion of ETB receptors, which is associated with elevated plasma levels of ET-1, would also reduce ETA expression in the periphery. In longitudinal sections from wild-type mice, the highest densities of ETA receptors localized to major organs including the ventricle of the heart, lung, and liver parenchyma. High densities of ETA receptors were detected in the smooth muscle layer of the vasculature such as intrarenal vessels as well as the smooth muscle layer and epithelial cells of the gastrointestinal tract. In these tissues, the ETA subtype was more abundant, representing between 60% and 100% of the ET receptors. ETB receptors predominated in the medulla of kidney, with high densities also localizing to glomeruli within the cortex and to the sinusoids from the liver. Lower densities of ETB receptors were also present in the lung, heart, liver, and the smooth muscle layer of the gastrointestinal tract. In ETB– /– knockout mice, ETB receptors were not detected as expected by either ligand binding or immunocytochemistry. The pattern of ETA receptor distribution in the ETB– /– knockout mice was similar to the controls, but the density of ETA receptors was significantly reduced in the lung by 39%. Diminished responses to the endogenous agonist after repeated stimulation are an important feature of G-protein signaling, preventing potential damage to the overstimulated cell, and it is likely that downregulation occurs in response to higher circulating levels of ET-1.

Key Words: image analysis • knockout mouse • quantitative autoradiography • radioligand binding




This article has been cited by other articles:


Home page
Am. J. Physiol. Gastrointest. Liver Physiol.Home page
J. Zhang, Y. Ling, L. Tang, B. Luo, D. M. Pollock, and M. B. Fallon
Attenuation of experimental hepatopulmonary syndrome in endothelin B receptor-deficient rats
Am J Physiol Gastrointest Liver Physiol, April 1, 2009; 296(4): G704 - G708.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2006 by the Society for Experimental Biology and Medicine.