脊椎动物在鸟类大脑中古老视蛋白的光探测假说。

IF 4.1 4区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Tyler J. Stevenson, Timothy A. Liddle, Simone L. Meddle, Jonathan H. Pérez, Stuart N. Peirson, Russell G. Foster, Gaurav Majumdar
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引用次数: 0

摘要

视网膜外的光接受在鱼类和鸟类中很常见。在鸟类中,下丘脑含有非视觉光感受器,可以探测光线并调节多种内分泌系统。迄今为止,季节性繁殖的光依赖控制是研究得最充分的系统之一,它需要大脑深层光接收。然而,检测光的精确光感受器以及视蛋白表达细胞和促性腺激素释放激素-1 (GnRH1)系统之间的神经内分泌联系仍然不清楚。在过去的几十年里,人们提出了两种视蛋白分子将鸟类的光探测与季节性繁殖联系起来:神经视蛋白(Opn5)和脊椎动物古代视蛋白(VA opsin)。只有VA视蛋白在GnRH1细胞中表达,其吸收光谱与鸟类光周期生殖反应的作用光谱相匹配。这一观点描述了白昼长度的年度变化(称为光周期)如何调节季节性生殖的神经内分泌控制。然后概述了视蛋白基因,并描述了细胞光导级联,突出了响应光刺激的超极化的共同特征。然后,我们讨论了使用短发夹RNA暂时敲低VA视蛋白和Opn5参与生殖神经内分泌调节转录本的最新证据。基于新出现的数据,我们概述了VA视蛋白可能调节鸟类GnRH1合成和释放的三种理论情景。提出的模型提供了一系列可测试的假设,可用于提高我们对VA视蛋白或大脑中其他表达视蛋白的细胞对鸟类光的检测的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hypotheses in light detection by vertebrate ancient opsin in the bird brain

Hypotheses in light detection by vertebrate ancient opsin in the bird brain

Extra-retinal photoreception is common across fish and avian species. In birds, the hypothalamus contains non-visual photoreceptors that detect light and regulate multiple endocrine systems. To date, light-dependent control of seasonal reproduction is one of the most well-studied systems that require deep brain photoreception. However, the precise photoreceptor(s) that detect light and the neuroendocrine connection between opsin-expressing cells and the gonadotropin-releasing hormone-1 (GnRH1) system remain poorly defined. In the past couple of decades, two opsin molecules have been proposed to link light detection with seasonal reproduction in birds: neuropsin (Opn5) and vertebrate ancient opsin (VA opsin). Only VA opsin is expressed in GnRH1 cells and has an absorption spectrum that matches the action spectrum of the avian photoperiodic reproductive response. This perspective describes how the annual change in daylength, referred to as photoperiod, regulates the neuroendocrine control of seasonal reproduction. The opsin genes are then outlined, and the cellular phototransduction cascade is described, highlighting the common feature of hyperpolarization in response to light stimulation. We then discuss the latest evidence using short-hairpin RNA to temporarily knock down VA opsin and Opn5 on transcripts involved in the neuroendocrine regulation of reproduction. Based on emerging data, we outline three theoretical scenarios in which VA opsin might regulate GnRH1 synthesis and release in birds. The models proposed provide a series of testable hypotheses that can be used to improve our understanding of avian light detection by VA opsin or other opsin-expressing cells in the brain.

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来源期刊
Journal of Neuroendocrinology
Journal of Neuroendocrinology 医学-内分泌学与代谢
CiteScore
6.40
自引率
6.20%
发文量
137
审稿时长
4-8 weeks
期刊介绍: Journal of Neuroendocrinology provides the principal international focus for the newest ideas in classical neuroendocrinology and its expanding interface with the regulation of behavioural, cognitive, developmental, degenerative and metabolic processes. Through the rapid publication of original manuscripts and provocative review articles, it provides essential reading for basic scientists and clinicians researching in this rapidly expanding field. In determining content, the primary considerations are excellence, relevance and novelty. While Journal of Neuroendocrinology reflects the broad scientific and clinical interests of the BSN membership, the editorial team, led by Professor Julian Mercer, ensures that the journal’s ethos, authorship, content and purpose are those expected of a leading international publication.
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