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生物发光作为一种用于可视化和控制神经元活动的功能性工具。

Bioluminescence as a functional tool for visualizing and controlling neuronal activity .

作者信息

Porta-de-la-Riva Montserrat, Morales-Curiel Luis-Felipe, Carolina Gonzalez Adriana, Krieg Michael

机构信息

ICFO-Institut de Ciències Fotòniques, The Barcelona Institute of Science and Technology, Castelldefels, Barcelona, Spain.

出版信息

Neurophotonics. 2024 Apr;11(2):024203. doi: 10.1117/1.NPh.11.2.024203. Epub 2024 Feb 12.

DOI:10.1117/1.NPh.11.2.024203
PMID:38348359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10861157/
Abstract

The use of bioluminescence as a reporter for physiology in neuroscience is as old as the discovery of the calcium-dependent photon emission of aequorin. Over the years, luciferases have been largely replaced by fluorescent reporters, but recently, the field has seen a renaissance of bioluminescent probes, catalyzed by unique developments in imaging technology, bioengineering, and biochemistry to produce luciferases with previously unseen colors and intensity. This is not surprising as the advantages of bioluminescence make luciferases very attractive for noninvasive, longitudinal observations without the need of an excitation light source. Here, we review how the development of dedicated and specific sensor-luciferases afforded, among others, transcranial imaging of calcium and neurotransmitters, or cellular metabolites and physical quantities such as forces and membrane voltage. Further, the increased versatility and light output of luciferases have paved the way for a new field of functional bioluminescence optogenetics, in which the photon emission of the luciferase is coupled to the gating of a photosensor, e.g., a channelrhodopsin and we review how they have been successfully used to engineer synthetic neuronal connections. Finally, we provide a primer to consider important factors in setting up functional bioluminescence experiments, with a particular focus on the genetic model , and discuss the leading challenges that the field needs to overcome to regain a competitive advantage over fluorescence modalities. Together, our paper caters to experienced users of bioluminescence as well as novices who would like to experience the advantages of luciferases in their own hand.

摘要

在神经科学中,将生物发光用作生理学报告分子的历史与水母发光蛋白钙依赖性光子发射的发现一样悠久。多年来,荧光素酶在很大程度上已被荧光报告分子所取代,但最近,由于成像技术、生物工程和生物化学方面的独特发展,能够产生具有前所未有的颜色和强度的荧光素酶,该领域见证了生物发光探针的复兴。这并不奇怪,因为生物发光的优势使荧光素酶对于无需激发光源的非侵入性纵向观察非常有吸引力。在这里,我们回顾了专用和特定的传感器荧光素酶的发展如何实现了钙、神经递质、细胞代谢物以及诸如力和膜电压等物理量的经颅成像。此外,荧光素酶增加的多功能性和光输出为功能性生物发光光遗传学的新领域铺平了道路,其中荧光素酶的光子发射与光传感器(例如,通道视紫红质)的门控相耦合,我们回顾了它们如何成功用于构建合成神经元连接。最后,我们提供了一个入门指南,以考虑在设置功能性生物发光实验时的重要因素,特别关注遗传模型,并讨论该领域为重新获得相对于荧光模式的竞争优势而需要克服的主要挑战。我们的论文共同面向生物发光的有经验用户以及希望亲身体验荧光素酶优势的新手。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce54/10861157/4e20c16c16f5/NPh-011-024203-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce54/10861157/d2e577c3e9a1/NPh-011-024203-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce54/10861157/7ef2b905ae7b/NPh-011-024203-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce54/10861157/7278cc25d52f/NPh-011-024203-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce54/10861157/2475d4dc53bc/NPh-011-024203-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce54/10861157/4e20c16c16f5/NPh-011-024203-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce54/10861157/d2e577c3e9a1/NPh-011-024203-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce54/10861157/7ef2b905ae7b/NPh-011-024203-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce54/10861157/7278cc25d52f/NPh-011-024203-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce54/10861157/2475d4dc53bc/NPh-011-024203-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce54/10861157/4e20c16c16f5/NPh-011-024203-g005.jpg

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本文引用的文献

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