Nelson Laura E, Sheridan Mark A
Department of Biological Sciences, North Dakota State University, Fargo, ND 58105, USA.
Gen Comp Endocrinol. 2005 May 15;142(1-2):117-33. doi: 10.1016/j.ygcen.2004.12.002. Epub 2005 Feb 1.
The multifunctional nature of the somatostatin (SS) family of peptides results from a multifaceted signaling system consisting of many forms of SS peptides that bind to a variety of receptor (SSTR) subtypes. Research in fish has contributed important information about the components, function, evolution, and regulation of this system. Somatostatins or mRNAs encoding SSs have been isolated from over 20 species of fish. Peptides and deduced peptides differ in their amino acid chain length and/or composition, and most species of fish possess more than one form of SS. The structural heterogeneity of SSs results from differential processing of the hormone precursor, preprosomatostatin (PPSS), and from the existence of multiple genes that give rise to multiple PPSSs. The PPSS genes appear to have arisen through a series of gene duplication events over the course of vertebrate evolution. The numerous PPSSs of fish are differentially expressed, both in terms of the distribution among tissues and in terms of the relative abundance within a tissue. Accumulated evidence suggests that nutritional state, season/stage of sexual maturation, and many hormones [insulin (INS), glucagon, growth hormone (GH), insulin-like growth factor-I (IGF-I), and 17beta-estradiol (E2)] regulate the synthesis and release of particular SSs. Fish and mammals possess multiple SSTRs; four different SSTRs have been described in fish and several of these occur as isoforms. SSTRs are also wide spread and are differentially expressed, both in terms of distribution of tissues as well as in terms of relative abundance within tissues. The pattern of distribution of SSTRs may underlie tissue-specific responses of SSs. The synthesis of SSTR mRNA and SS-binding capacity are regulated by nutritional state and numerous hormones (INS, GH, IGF-I, and E2). Accumulated evidence suggests the possibility of both tissue- and subtype-specific mechanisms of regulation. In many instances, there appears to be coordinate regulation of PPSS and of SSTR; such regulation may prove important for many processes, including nutrient homeostasis and growth control.
生长抑素(SS)肽家族的多功能特性源于一个多方面的信号系统,该系统由多种形式的SS肽组成,这些肽可与多种受体(SSTR)亚型结合。鱼类研究为该系统的组成、功能、进化和调节提供了重要信息。已从20多种鱼类中分离出生长抑素或编码SS的mRNA。肽和推导的肽在氨基酸链长度和/或组成上有所不同,大多数鱼类物种拥有不止一种形式的SS。SS的结构异质性源于激素前体前生长抑素(PPSS)的差异加工,以及产生多个PPSS的多个基因的存在。PPSS基因似乎是在脊椎动物进化过程中通过一系列基因复制事件产生的。鱼类众多的PPSS在组织分布和组织内相对丰度方面均有差异表达。积累的证据表明,营养状态、性成熟的季节/阶段以及许多激素[胰岛素(INS)、胰高血糖素、生长激素(GH)、胰岛素样生长因子-I(IGF-I)和17β-雌二醇(E2)]调节特定SS的合成和释放。鱼类和哺乳动物都拥有多种SSTR;在鱼类中已描述了四种不同的SSTR,其中几种以异构体形式存在。SSTR也广泛分布且差异表达,无论是在组织分布还是组织内相对丰度方面。SSTR的分布模式可能是SS组织特异性反应的基础。SSTR mRNA的合成和SS结合能力受营养状态和多种激素(INS、GH、IGF-I和E2)调节。积累的证据表明存在组织特异性和亚型特异性调节机制的可能性。在许多情况下,PPSS和SSTR似乎存在协同调节;这种调节可能对许多过程(包括营养稳态和生长控制)很重要。