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鉴定尾加压素II相关肽为大鼠脑中尾加压素II免疫反应性分子。

Identification of urotensin II-related peptide as the urotensin II-immunoreactive molecule in the rat brain.

作者信息

Sugo Tsukasa, Murakami Yuko, Shimomura Yukio, Harada Mioko, Abe Michiko, Ishibashi Yoshihiro, Kitada Chieko, Miyajima Nobuyuki, Suzuki Nobuhiro, Mori Masaaki, Fujino Masahiko

机构信息

Discovery Research Laboratories, Pharmaceutical Research Division, Takeda Chemical Industries, Ltd., Tsukuba, Ibaraki, Japan.

出版信息

Biochem Biophys Res Commun. 2003 Oct 24;310(3):860-8. doi: 10.1016/j.bbrc.2003.09.102.

Abstract

Urotensin II (UII) has been reported as the most potent known vasoconstrictor. While rat and mouse orthologs of UII precursor protein have been reported, only the tentative structures of UII peptides of these animals have been demonstrated, since prepro-UII proteins lack typical processing sites for their mature peptides. In the present study, we isolated a novel peptide, UII-related peptide (URP), from the extract of the rat brain as the sole immunoreactive substance to anti-UII antibody; the amino acid sequence of the peptide was determined as ACFWKYCV. cDNAs encoding rat, mouse, and human precursor proteins for URP were cloned and revealed that the sequences of mouse and human URP peptides are the same as that for rat URP. Prepro-URP gene is expressed in several rat tissues such as those of the thymus, spleen, testis, and spinal cord, although with lower levels than the prepro-UII gene. In the human, the prepro-URP gene is expressed comparably to prepro-UII in several tissues except the spinal cord. URP was found to bind and activate the human or rat UII receptors (GPR14) and showed a hypotensive effect when administered to anesthetized rats. These results suggest that URP is the endogenous and functional ligand for UII receptor in the rat and mouse, and possibly in the human. We also describe the preparation of specific monoclonal antibodies raised against UII peptide and the establishment of a highly sensitive enzyme immunoassay system for UII peptides.

摘要

尾加压素II(UII)据报道是已知最强效的血管收缩剂。虽然已报道了UII前体蛋白的大鼠和小鼠直系同源物,但由于前UII蛋白缺乏成熟肽的典型加工位点,这些动物的UII肽的结构仅为初步确定。在本研究中,我们从大鼠脑提取物中分离出一种新型肽,即UII相关肽(URP),它是抗UII抗体的唯一免疫反应性物质;该肽的氨基酸序列确定为ACFWKYCV。克隆了编码大鼠、小鼠和人前体蛋白的URP的cDNA,结果显示小鼠和人URP肽的序列与大鼠URP相同。前URP基因在大鼠的多个组织中表达,如胸腺、脾脏、睾丸和脊髓,但表达水平低于前UII基因。在人类中,除脊髓外,前URP基因在多个组织中的表达水平与前UII相当。发现URP可结合并激活人或大鼠的UII受体(GPR14),并在麻醉大鼠给药时显示出降压作用。这些结果表明,URP是大鼠和小鼠以及可能在人类中UII受体的内源性和功能性配体。我们还描述了针对UII肽产生的特异性单克隆抗体的制备以及UII肽高灵敏度酶免疫分析系统的建立。

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