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利钠肽信号传导:生长调节的分子和细胞途径

Natriuretic peptide signalling: molecular and cellular pathways to growth regulation.

作者信息

Silberbach M, Roberts C T

机构信息

Division of Pediatric Cardiology, Department of Pediatrics, Doernbecher Children's Hospital, UHN-60, 3181 SW Sam Jackson Park Road, 97201, Portland, OR, USA.

出版信息

Cell Signal. 2001 Apr;13(4):221-31. doi: 10.1016/s0898-6568(01)00139-5.

Abstract

The natriuretic peptides (NPs) constitute a family of polypeptide hormones that regulate mammalian blood volume and blood pressure. The ability of the NPs to modulate cardiac hypertrophy and cell proliferation as well is now beginning to be recognized. The NPs interact with three membrane-bound receptors, all of which contain a well-characterized extracellular ligand-binding domain. The R1 subclass of NP receptors (NPR-A and NPR-B) contains a C-terminal guanylyl cyclase domain and is responsible for most of the NPs downstream actions through their ability to generate cGMP. The R2 subclass lacks an obvious catalytic domain and functions primarily as a clearance receptor. This review focuses on the signal transduction pathways initiated by ligand binding and other factors that help to determine signalling specificities, including allosteric factors modulating cGMP generation, receptor desensitization, the activation and function of cGMP-dependent protein kinase (PKG), and identification of potential nuclear or cytoplasmic targets such as the mitogen-activated protein kinase signalling (MAPK) cascade. The inhibition of cardiac growth and hypertrophy may be an important but underappreciated action of the NP signalling system.

摘要

利钠肽(NPs)构成了一类调节哺乳动物血容量和血压的多肽激素家族。现在人们也开始认识到NPs调节心脏肥大和细胞增殖的能力。NPs与三种膜结合受体相互作用,所有这些受体都含有一个特征明确的细胞外配体结合结构域。NP受体的R1亚类(NPR - A和NPR - B)含有一个C末端鸟苷酸环化酶结构域,并通过其产生cGMP的能力负责NPs的大部分下游作用。R2亚类缺乏明显的催化结构域,主要作为清除受体发挥作用。本综述重点关注由配体结合引发的信号转导途径以及有助于确定信号特异性的其他因素,包括调节cGMP生成的变构因子、受体脱敏、cGMP依赖性蛋白激酶(PKG)的激活和功能,以及识别潜在的核或细胞质靶点,如丝裂原活化蛋白激酶信号(MAPK)级联反应。抑制心脏生长和肥大可能是NP信号系统的一个重要但未得到充分认识的作用。

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