|
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.

CiteULike Complore Connotea Del.icio.us Digg Reddit Technorati What's this?
This article has been cited by other articles:

|
 |

|
 |
 
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]
|
 |
|

|
 |

|
 |
 
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]
|
 |
|

|
 |

|
 |
 
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]
|
 |
|

|
 |

|
 |
 
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]
|
 |
|

|
 |

|
 |
 
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]
|
 |
|

|
 |

|
 |
 
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]
|
 |
|

|
 |

|
 |
 
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]
|
 |
|

|
 |

|
 |
 
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]
|
 |
|

|
 |

|
 |
 
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]
|
 |
|

|
 |

|
 |
 
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]
|
 |
|
Copyright © 1986 by the American Society for Biochemistry and Molecular Biology.
|
Advertisement
Advertisement
|