Label-free imaging of neurotransmitters in live brain tissue by multi-photon ultraviolet microscopy.

Q4 Neuroscience Neuronal signaling Pub Date : 2018-12-03 eCollection Date: 2018-12-01 DOI:10.1042/NS20180132
Barun Kumar Maity, Sudipta Maiti
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引用次数: 10

Abstract

Visualizing small biomolecules in living cells remains a difficult challenge. Neurotransmitters provide one of the most frustrating examples of this difficulty, as our understanding of signaling in the brain critically depends on our ability to follow the neurotransmitter traffic. Last two decades have seen considerable progress in probing some of the neurotransmitters, e.g. by using false neurotransmitter mimics, chemical labeling techniques, or direct fluorescence imaging. Direct imaging harnesses the weak UV fluorescence of monoamines, which are some of the most important neurotransmitters controlling mood, memory, appetite, and learning. Here we describe the progress in imaging of these molecules using the least toxic direct excitation route found so far, namely multi-photon (MP) imaging. MP imaging of serotonin, and more recently that of dopamine, has allowed researchers to determine the location of the vesicles, follow their intracellular dynamics, probe their content, and monitor their release. Recent developments have even allowed ratiometric quantitation of the vesicular content. This review shows that MP ultraviolet (MP-UV) microscopy is an effective but underutilized method for imaging monoamine neurotransmitters in neurones and brain tissue.

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多光子紫外显微镜下活体脑组织中神经递质的无标记成像。
可视化活细胞中的小生物分子仍然是一个困难的挑战。神经递质是这一难题中最令人沮丧的例子之一,因为我们对大脑信号的理解严重依赖于我们追踪神经递质交通的能力。过去二十年来,在探测某些神经递质方面取得了相当大的进展,例如使用假神经递质模拟、化学标记技术或直接荧光成像。直接成像利用单胺的弱紫外荧光,单胺是控制情绪、记忆、食欲和学习的一些最重要的神经递质。在这里,我们描述了利用迄今为止发现的毒性最小的直接激发途径,即多光子(MP)成像这些分子的进展。血清素的MP成像,以及最近的多巴胺成像,使研究人员能够确定囊泡的位置,跟踪它们的细胞内动力学,探测它们的含量,并监测它们的释放。最近的发展甚至允许对囊泡含量进行比例定量。这一综述表明,MP- uv显微镜是一种有效但未充分利用的成像神经元和脑组织中单胺类神经递质的方法。
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来源期刊
CiteScore
4.60
自引率
0.00%
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0
审稿时长
14 weeks
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