Gonzalez R, Unniappan S
Department of Biology, York University, Toronto, ON, Canada.
Laboratory of Integrative Neuroendocrinology, Department of Veterinary Biomedical Sciences, Western College of Veterinary Medicine, University of Saskatchewan, Saskatoon, SK, S7N 5B4, Canada.
Fish Physiol Biochem. 2016 Jun;42(3):831-44. doi: 10.1007/s10695-015-0178-y. Epub 2015 Dec 16.
Dipeptidyl peptidase-4 (DPP4) is a serine protease of great interest because it has been shown to modulate the activity of several peptidergic factors including peptide YY (PYY) and glucagon-like peptide-1/2. While PYY(1-36) is orexigenic in mammals, PYY(3-36) recently garnered interest as a potent anorexigen. In silico phylogenetic analysis found that the DPP4 cleavage sites are absent in fish PYY sequences. However, no studies were conducted to show that indeed PYY(3-36) is not produced by DPP4 in fish. If DPP4 does not cleave PYY(1-36), is PYY(3-36) an anorexigen in fish? The objectives of this research were to (1) test whether DPP4 cleaves goldfish PYY(1-36) and (2) determine whether PYY(3-36) is an anorexigen in goldfish. First, we identified the highly conserved catalytic region of DPP4 in goldfish. Abundant expression of DPP4 mRNA was found within the gastrointestinal tract. We also report the first MALDI-MS cleavage analysis of DPP4 effects on PYY(1-36) in a non-mammalian vertebrate. Our novel results indicate that DPP4 is unable to cleave goldfish PYY(1-36) to PYY(3-36) in vitro. It also confirms a previously held hypothesis that DPP4 is unable to cleave fish PYY(1-36) that contains N-terminal proline-proline residues. PYY(3-36) had no effects on food intake of goldfish. The appetite inhibitory effects of intraperitoneal and intracerebroventricular injections of 10 ng/g body weight gfPYY(1-36) were abolished by coinjections of BIBP3226, a Y1 receptor antagonist. These results are significant because it shows the lack of generation of endogenous PYY(3-36) and its anorectic effects in goldfish.
二肽基肽酶-4(DPP4)是一种备受关注的丝氨酸蛋白酶,因为它已被证明可调节多种肽能因子的活性,包括肽YY(PYY)和胰高血糖素样肽-1/2。虽然PYY(1-36)在哺乳动物中具有促食欲作用,但PYY(3-36)最近作为一种强效的食欲抑制剂引起了人们的兴趣。在计算机系统发育分析中发现,鱼类PYY序列中不存在DPP4切割位点。然而,尚未有研究表明鱼类中的DPP4确实不会产生PYY(3-36)。如果DPP4不切割PYY(1-36),那么PYY(3-36)在鱼类中是一种食欲抑制剂吗?本研究的目的是:(1)测试DPP4是否切割金鱼的PYY(1-36);(2)确定PYY(3-36)在金鱼中是否为食欲抑制剂。首先,我们鉴定了金鱼中DPP4高度保守的催化区域。在胃肠道中发现了丰富的DPP4 mRNA表达。我们还首次报道了在非哺乳动物脊椎动物中对DPP4对PYY(1-36)作用的基质辅助激光解吸电离质谱(MALDI-MS)切割分析。我们的新结果表明,DPP4在体外无法将金鱼的PYY(1-36)切割为PYY(3-36)。这也证实了之前的一个假设,即DPP4无法切割含有N端脯氨酸-脯氨酸残基的鱼类PYY(1-36)。PYY(3-36)对金鱼的食物摄入量没有影响。腹腔和脑室内注射10 ng/g体重的金鱼PYY(1-36)的食欲抑制作用被共同注射的Y1受体拮抗剂BIBP3226消除。这些结果具有重要意义,因为它们表明金鱼中缺乏内源性PYY(3-36)的产生及其食欲抑制作用。