Natriuretic peptide receptor-C signaling and regulation

被引:201
作者
Anand-Srivastava, MB
机构
[1] Univ Montreal, Fac Med, Dept Physiol, Montreal, PQ H3C 3J7, Canada
[2] Univ Montreal, Grp Rech Syst Nerveux Autonome, Fac Med, Montreal, PQ H3C 3J7, Canada
基金
加拿大健康研究院;
关键词
natriuretic peptides; NPR-C receptor; adenylyl cyclase; PI turnover;
D O I
10.1016/j.peptides.2004.09.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The natriuretic peptides (NP) are a family of three polypeptide hormones termed atrial natriuretic peptide (ANP). brain natriuretic peptide (BNP), and C-type natriuretic peptide (CNP). ANP regulates a variety of physiological parameters by interacting with its receptors present on the plasma membrane. These are of three subtypes NPR-A, NPR-B, and NPR-C. NPR-A and NPR-B are guanylyl cyclase receptors, whereas NPR-C is non-guanylyl cyclase receptor and is coupled to adenylyl cyclase inhibition or phospholipase C activation through inhibitory guanine nucleotide regulatory protein (Gi). ANP, BNP, CNP. as well as C-ANP(4) (23). a ring deleted peptide that specifically interacts with NPR-C receptor inhibit adenylyl cyclase activity through Gi protein. Unlike other G-protein-coupled receptors. NPR-C receptors have a single transmembrane domain and a short cytoplasmic domain of 37 amino acids, which has a structural specificity like those of other single transmembrane domain receptors. A 37 amino acid cytoplasmic peptide is sufficient to inhibit adenylyl cyclase activity with art apparent Ki similar to that of ANP(99, 126) or C-ANP(4-23). In addition, C-ANP(4-23) also stimulates phosphatidyl inositol (PI) turnover in vascular smooth muscle cells (VSMC) which is attenuated by dbcAMP and cAMP-stimulatory agonists, suggesting that NPR-C receptor-mediated inhibition of adenylyl cyclase and resultant decreased levels of cAMP may be responsible for NPR-C-mediated stimulation of PI turnover. Furthermore, the activation of NPR-C receptor by C-ANP4-23 and CNP inhibits the mitogen-activated protein kinase activity stimulated by endothelin-3, platelet-derived growth factor, phorbol-12 myristate 13-acetate. suggesting that NPR-C receptor might also be coupled to other signal transduction system or that there may be an interaction of the NPR-C receptor and some other signaling pathways, In this review article. NPR-C receptor coupling to different signaling pathways and their regulation will be discussed. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1044 / 1059
页数:16
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