Advertisement
JBC

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
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
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Leitman, D. C.
Right arrow Articles by Murad, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Leitman, D. C.
Right arrow Articles by Murad, F.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

J. Biol. Chem., Vol. 261, Issue 25, 11650-11655, 09, 1986

Identification of multiple binding sites for atrial natriuretic factor by affinity cross-linking in cultured endothelial cells

DC Leitman, JW Andresen, T Kuno, Y Kamisaki, JK Chang and F Murad

In a previous study, we found that atriopeptin I was much weaker (EC50 greater than 500 nM) than atrial natriuretic factor (ANF-(8-33)) (EC50 = 0.3 nM) at increasing cyclic GMP in cultured endothelial cells. In this study, we used the cross-linking reagent disuccinimidyl suberate to investigate whether the differences in activity were due to the presence of multiple ANF receptors. When 98% of the ANF-binding sites on endothelial cells were occupied by tyrosine-atriopeptin I after cross-linking, there was no difference in the concentration-response curve to ANF-(8-33) with regard to cyclic GMP accumulation. In contrast, when 96% of the binding sites were occupied by cross-linked ANF-(8-33), a 60% decrease in the maximal cyclic GMP response was observed after the readdition of ANF-(8-33). These results suggest that ANF-(8-33) is binding to an additional site that atriopeptin I does not effectively bind. Affinity cross-linking of 125I-ANF to intact endothelial cells resulted in the labeling of two sites of Mr approximately 66,000 and approximately 130,000. Approximately 94% of the 125I-ANF binding sites had an Mr approximately 66,000. Labeling of this site was inhibited by both tyrosine-atriopeptin I (KI = 0.9 nM) and ANF-(8-33) (KI = 0.09 nM). Although 0.1 microM tyrosine-atriopeptin (AP I) inhibited labeling of the 66,000-dalton site to nearly the same degree as ANF-(8-33), it produced only a 4-fold increase in cyclic GMP compared to a 400-fold increase with ANF-(8-33). These results suggest that the 66,000-dalton site is not coupled to guanylate cyclase and cyclic GMP formation. Tyrosine-AP I (KI greater than 10 nM) was much weaker at competing for the 130,000-dalton site than ANF-(8-33) (KI = 0.075 nM). Because the EC50 for cyclic GMP stimulation for tyrosine-AP I (greater than 100 nM) and ANF-(8-33) (0.4 nM) is closer to the KI values for the 130,000-dalton protein, this site probably mediates the marked stimulation of cyclic GMP. Our results demonstrate that endothelial cells contain two binding sites for ANF-(8-33) and suggest that only the less abundant site (Mr approximately 130,000) is the receptor coupled to the activation of guanylate cyclase.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
EndocrinologyHome page
B. Schreier, S. Borner, K. Volker, S. Gambaryan, S. C. Schafer, P. Kuhlencordt, B. Gassner, and M. Kuhn
The Heart Communicates with the Endothelium through the Guanylyl Cyclase-A Receptor: Acute Handling of Intravascular Volume in Response to Volume Expansion
Endocrinology, August 1, 2008; 149(8): 4193 - 4199.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
K. Sabrane, S. Gambaryan, R. P. Brandes, R. Holtwick, M. Voss, and M. Kuhn
Increased Sensitivity to Endothelial Nitric Oxide (NO) Contributes to Arterial Normotension in Mice with Vascular Smooth Muscle-selective Deletion of the Atrial Natriuretic Peptide (ANP) Receptor
J. Biol. Chem., May 9, 2003; 278(20): 17963 - 17968.
[Abstract] [Full Text] [PDF]


Home page
Cardiovasc ResHome page
F. Brunner and G. Wolkart
Relaxant effect of C-type natriuretic peptide involves endothelium and nitric oxide-cGMP system in rat coronary microvasculature
Cardiovasc Res, August 15, 2001; 51(3): 577 - 584.
[Abstract] [Full Text] [PDF]


Home page
Physiol. GenomicsHome page
L. G. MELO, M. E. STEINHELPER, S. C. PANG, Y. TSE, and U. ACKERMANN
ANP in regulation of arterial pressure and fluid-electrolyte balance: lessons from genetic mouse models
Physiol Genomics, June 29, 2000; 3(1): 45 - 58.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
L. G. Melo, A. T. Veress, U. Ackermann, and H. Sonnenberg
Chronic regulation of arterial blood pressure by ANP: role of endogenous vasoactive endothelial factors
Am J Physiol Heart Circ Physiol, November 1, 1998; 275(5): H1826 - H1833.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
K. Fujishige, N. Yanaka, H. Akatsuka, and K. Omori
Localization of clearance receptor in rat lung and trachea: association with chondrogenic differentiation
Am J Physiol Lung Cell Mol Physiol, March 1, 1998; 274(3): L425 - L431.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
J.-P. Valentin, W.-Z. Ying, W. G. Couser, and M. H. Humphreys
Extrarenal resistance to atrial natriuretic peptide in rats with experimental nephrotic syndrome
Am J Physiol Renal Physiol, March 1, 1998; 274(3): F556 - F563.
[Abstract] [Full Text] [PDF]


Home page
HypertensionHome page
D. W. Zlock, L. Cao, J. Wu, and D. G. Gardner
Thrombin Inhibits Atrial Natriuretic Peptide Receptor Activity in Cultured Bovine Endothelial Cells
Hypertension, January 1, 1997; 29(1): 83 - 90.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
T. Abe, Y. Arakawa, A. K. Rajasekaran, T.-H. Yu, and O. Wada
Interaction of Atrial Natriuretic Peptide with Its Receptors in Bovine Lung Membranes
J. Biol. Chem., March 31, 1995; 270(13): 7672 - 7678.
[Abstract] [Full Text] [PDF]


Home page
Cold Spring Harb Symp Quant BiolHome page
F. Murad, D. Leitman, S. Waldman, C.-H. Chang, M. Hirata, and K. Kohse
Effects of Nitrovasodilators, Endothelium-dependent Vasodilators, and Atrial Peptides on cGMP
Cold Spring Harb Symp Quant Biol, January 1, 1988; 53(0): 1005 - 1009.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Molecular and Cellular Proteomics 
 Journal of Lipid Research   ASBMB Today 
Copyright © 1986 by the American Society for Biochemistry and Molecular Biology.
Advertisement
spacer
Advertisement
Advertisement