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多光子显微镜用于周围神经的无标记多色成像。

Multiphoton microscopy for label-free multicolor imaging of peripheral nerve.

机构信息

Boston University, Department of Electrical and Computer Engineering, Boston, Massachusetts, United States.

Technical University of Denmark, DTU Fotonik, Kgs. Lyngby, Denmark.

出版信息

J Biomed Opt. 2022 May;27(5). doi: 10.1117/1.JBO.27.5.056501.

DOI:10.1117/1.JBO.27.5.056501
PMID:35568795
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9109936/
Abstract

SIGNIFICANCE

Means for quantitation of myelinated fibers in peripheral nerve may guide diagnosis and clinical decision making in management of peripheral nerve disorders. Multiphoton microscopy techniques such as the third-harmonic generation enable label-free in vivo imaging of peripheral nerves.

AIM

Develop a multiphoton microscope based on a custom high-power infrared fiber laser for label-free imaging of peripheral nerve.

APPROACH

A cost-effective multiphoton microscope employing a single fiber laser source at 1300 nm was designed and used for stain-free multicolor imaging of murine and human peripheral nerve.

RESULTS

Second-harmonic generation signal from collagen centered about 650-nm delineated neural connective tissue, whereas third-harmonic general signal centered about 433-nm delineated myelin and other lipids. In sciatic nerve from transgenic reporter mice expressing yellow fluorescent protein within peripheral neurons, three-photon-excitation with emission peak at 527-nm delineated axoplasm. The signal obtained from unlabeled axially sectioned samples was adequate for segmentation of myelinated fibers using commercial image processing software. In unlabeled whole mount specimens, imaging depths over 100-μm were achieved.

CONCLUSIONS

A multiphoton microscope powered by a fiber laser enables stain-free histomorphometry of mammalian peripheral nerve. The simplicity of the microscope design carries potential for clinical translation to inform decision making in peripheral nerve disorders.

摘要

意义

用于量化周围神经髓鞘纤维的方法可以指导周围神经疾病管理中诊断和临床决策的制定。多光子显微镜技术,如三次谐波产生,可实现周围神经的无标记体内成像。

目的

开发一种基于定制高功率红外光纤激光器的多光子显微镜,用于无标记成像周围神经。

方法

设计了一种具有成本效益的多光子显微镜,采用 1300nm 处的单个光纤激光源,用于对鼠和人周围神经进行无染色多色成像。

结果

胶原的二次谐波产生信号集中在 650nm 左右,描绘了神经结缔组织,而集中在 433nm 左右的三次谐波产生信号描绘了髓鞘和其他脂质。在表达黄色荧光蛋白的转基因报告小鼠的坐骨神经中,使用发射峰在 527nm 的三光子激发描绘了轴浆。使用商业图像处理软件对标记的轴向切片样本进行分割,获得的信号足以对有髓纤维进行分割。在未标记的整个安装标本中,实现了超过 100μm 的成像深度。

结论

由光纤激光器供电的多光子显微镜可实现哺乳动物周围神经的无染色组织形态计量学。该显微镜设计的简单性具有临床转化的潜力,可为周围神经疾病的决策提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a039/9109936/a5820b52c1fc/JBO-027-056501-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a039/9109936/2c9e9430f1e0/JBO-027-056501-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a039/9109936/d35a6129734a/JBO-027-056501-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a039/9109936/fbd1214178a1/JBO-027-056501-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a039/9109936/2291ab484251/JBO-027-056501-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a039/9109936/88b3b8f9a338/JBO-027-056501-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a039/9109936/b15de597e2b1/JBO-027-056501-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a039/9109936/a5820b52c1fc/JBO-027-056501-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a039/9109936/2c9e9430f1e0/JBO-027-056501-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a039/9109936/d35a6129734a/JBO-027-056501-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a039/9109936/fbd1214178a1/JBO-027-056501-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a039/9109936/2291ab484251/JBO-027-056501-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a039/9109936/88b3b8f9a338/JBO-027-056501-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a039/9109936/b15de597e2b1/JBO-027-056501-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a039/9109936/a5820b52c1fc/JBO-027-056501-g007.jpg

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