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长期研究中光敏感离子通道重复激活的考量:果蝇模型中的通道视紫红质

Considerations in repetitive activation of light sensitive ion channels for long-term studies: Channel rhodopsin in the Drosophila model.

作者信息

Higgins Jake, Hermanns Christina, Malloy Cole, Cooper Robin L

机构信息

University of Kentucky College of Nursing, University of Kentucky, Lexington, KY 40536, USA; Department of Biology and Center for Muscle Biology, University of Kentucky, Lexington, KY 40506, USA.

Department of Biology and Center for Muscle Biology, University of Kentucky, Lexington, KY 40506, USA.

出版信息

Neurosci Res. 2017 Dec;125:1-10. doi: 10.1016/j.neures.2017.07.001. Epub 2017 Jul 17.

Abstract

Optogenetics is a technique used in various animal models and holds a potential for therapeutic possibilities in mammals. There are technical issues with the use of light sensitive ion channels: reproducible effects over time, controlling where the non-native proteins are targeted within the cell and changes in the biophysical properties of the cells they are expressed in. We used a variant of channel rhodopsin (ChR2-XXL) and targeted expression in neurons of larval Drosophila to investigate the acute and chronic activation, with light pulses, of the channels on synaptic function. The rhodopsin channel modifier all trans retinal (ATR) also plays a role in the sensitivity of the channel to light. Periods of acute, repetitive, and pulsatile blue light exposure over larval development produced attenuated responses. These blue light sensitive ion channels, with ATR, show accommodation and produce an electrical refractory period in inducing synaptic responses. The biological significance and aim of this study is to demonstrate that in controlling particular neurons or neuronal circuits with optogenetics, over time and throughout development, one will have to understand the dynamic nature of activating and silencing the light sensitive channels as well as the biophysical effects on neuronal activity.

摘要

光遗传学是一种应用于多种动物模型的技术,在哺乳动物中具有治疗潜力。使用光敏离子通道存在技术问题:随着时间推移的可重复效应、控制非天然蛋白质在细胞内的靶向位置以及它们所表达细胞的生物物理特性变化。我们使用了一种通道视紫红质变体(ChR2 - XXL),并将其靶向表达于幼虫果蝇的神经元中,以研究光脉冲对通道的急性和慢性激活对突触功能的影响。视紫红质通道调节剂全反式视黄醛(ATR)也在通道对光的敏感性中起作用。在幼虫发育过程中,急性、重复性和脉冲性蓝光暴露会导致反应减弱。这些带有ATR的蓝光敏感离子通道表现出适应性,并在诱导突触反应时产生电不应期。本研究的生物学意义和目的是证明,在通过光遗传学控制特定神经元或神经回路时,随着时间推移和整个发育过程,必须了解激活和沉默光敏通道的动态性质以及对神经元活动的生物物理影响。

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