Lu Weiqun, Greenwood Michael, Dow Louise, Yuill Janette, Worthington Jonathan, Brierley Matthew J, McCrohan Catherine R, Riccardi Daniela, Balment Richard J
Faculty of Life Sciences, University of Manchester, Manchester M13 9PT, United Kingdom.
Endocrinology. 2006 Aug;147(8):3692-708. doi: 10.1210/en.2005-1457. Epub 2006 May 4.
Urotensin II (UII) is a potent vasoconstrictor in mammals, but the source of circulating UII remains unclear. Investigations of the caudal neurosecretory system (CNSS), considered the major source of UII in fish, alongside target tissue expression of UII receptor (UT), can provide valuable insights into this highly conserved regulatory system. We report UII gene characterization, expression of the first fish UT, and responses to salinity challenge in flounder. The 12-aa UII peptide shares 73% sequence identity with pig and human UII. Flounder UT receptor shares 56.7% identity with rat. Although the CNSS is the major site of UII expression, RT-PCR revealed expression of UII and UT in all tissues tested. Around 30-40% of large CNSS Dahlgren cells expressed UII, alone or in combination with urotensin I and/or corticotrophin releasing hormone. Immunolocalization of UT in osmoregulatory tissues (gill, kidney) was associated with vascular elements. There were no consistent differences in CNSS UII expression or plasma UII between seawater (SW)- and freshwater (FW)-adapted fish, although gill and kidney UT expression was lower in FW animals. After acute transfer from SW to FW, plasma UII and kidney and gill UT expression were reduced, whereas UT expression in kidney was increased after reverse transfer. UII appears to be more important to combat dehydration and salt-loading in SW than the hemodilution faced in FW. Potentially, altered target tissue sensitivity through changes in UT expression, is an important physiological controlling mechanism, not only relevant for migratory fish but also likely conserved in mammals.
尾加压素II(UII)是哺乳动物中一种强效的血管收缩剂,但循环中UII的来源仍不清楚。对被认为是鱼类UII主要来源的尾神经分泌系统(CNSS)进行研究,同时结合UII受体(UT)在靶组织中的表达情况,可为这个高度保守的调节系统提供有价值的见解。我们报告了比目鱼UII基因的特征、首个鱼类UT的表达以及对比目鱼盐度挑战的反应。12个氨基酸的UII肽与猪和人类的UII有73%的序列同一性。比目鱼UT受体与大鼠的受体有56.7%的同一性。尽管CNSS是UII表达的主要部位,但逆转录聚合酶链反应(RT-PCR)显示在所有测试组织中都有UII和UT的表达。大约30%-40%的大型CNSS达尔格伦细胞单独或与尾加压素I和/或促肾上腺皮质激素释放激素联合表达UII。UT在渗透调节组织(鳃、肾)中的免疫定位与血管成分有关。在适应海水(SW)和淡水(FW)的鱼类之间,CNSS中UII的表达或血浆UII没有一致的差异,尽管FW动物鳃和肾中的UT表达较低。从SW急性转移到FW后,血浆UII以及肾和鳃中的UT表达降低,而反向转移后肾中的UT表达增加。UII在对抗SW中的脱水和盐分负荷方面似乎比FW中面临的血液稀释更为重要。潜在地,通过UT表达的变化改变靶组织敏感性是一种重要的生理控制机制,不仅与洄游鱼类有关,而且可能在哺乳动物中也保守存在。