Selective Activation of the B Natriuretic Peptide Receptor by C-Type Natriuretic Peptide (CNP)

The natriuretic peptides are hormones that can stimulate natriuretic, diuretic, and vasorelaxant activity in vivo, presumably through the activation of two known cell surface receptor guanylyl cyclases (ANPR-A and ANPR-B). Although atrial natriuretic peptide (ANP) and, to a lesser extent, brain natr...

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Published inScience (American Association for the Advancement of Science) Vol. 252; no. 5002; pp. 120 - 123
Main Authors Koller, Kerry J., Lowe, David G., Bennett, Gregory L., Minamino, Naoto, Kangawa, Kenji, Matsuo, Hisayuki, Goeddel, David V.
Format Journal Article
LanguageEnglish
Published Washington, DC American Society for the Advancement of Science 05.04.1991
American Association for the Advancement of Science
The American Association for the Advancement of Science
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Summary:The natriuretic peptides are hormones that can stimulate natriuretic, diuretic, and vasorelaxant activity in vivo, presumably through the activation of two known cell surface receptor guanylyl cyclases (ANPR-A and ANPR-B). Although atrial natriuretic peptide (ANP) and, to a lesser extent, brain natriuretic peptide (BNP) are efficient activators of the ANPR-A guanylyl cyclase, neither hormone can significantly stimulate ANPR-B. A member of this hormone family, C-type natriuretic peptide (CNP), potently and selectively activated the human ANPR-B guanylyl cyclase. CNP does not increase guanosine 3′,5′-monophosphate accumulation in cells expressing human ANPR-A. The affinity of CNP for ANPR-B is 50- or 500-fold higher than ANP or BNP, respectively. This ligand-receptor pair may be involved in the regulation of fluid homeostasis by the central nervous system.
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ISSN:0036-8075
1095-9203
DOI:10.1126/science.1672777