{"title":"Wide-field fluorescence navigation system for efficient miniature multiphoton imaging in freely behaving animals.","authors":"Runlong Wu, Yukun Sun, Zeyu Hao, Chunzhu Zhao, Lishuang Feng, Aimin Wang, Heping Cheng","doi":"10.1117/1.NPh.12.2.025018","DOIUrl":null,"url":null,"abstract":"<p><strong>Significance: </strong>Miniature multiphoton microscopy has revolutionized neuronal imaging in freely behaving animals. However, its shallow depth of field-a result of high axial resolution-combined with a limited field of view (FOV), makes it challenging for researchers to identify regions of interest in three-dimensional space across multimillimeter cranial windows, thereby reducing the system's ease of use.</p><p><strong>Aim: </strong>We aimed to develop a multimodal imaging platform with enhanced guidance and a standardized workflow tailored for efficient imaging of freely behaving animals.</p><p><strong>Approach: </strong>We present a wide-field fluorescence navigation system (WF-Nav) featuring a 90-mm working distance, a 4-mm FOV, and single-cell resolution, enabling rapid and precise localization of designated regions. By seamlessly integrating this navigation system with our prior miniature multiphoton microscopes, we established a multimodal platform that supports versatile imaging modalities and seamless transitions to two- or three-photon imaging. Building on this integration, we developed a streamlined workflow for efficient, user-friendly imaging in freely behaving mice.</p><p><strong>Results: </strong>We validated the system through large-FOV imaging (4 mm), dual-color imaging (920 and 1030 nm), and deep-brain neuronal imaging (up to 1 mm) in either awake mice or freely moving mice. The entire experimental procedure was completed in <math><mrow><mo>∼</mo> <mn>20</mn> <mtext> </mtext> <mi>min</mi></mrow> </math> , achieving a 100% success rate ( <math><mrow><mi>n</mi> <mo>=</mo> <mn>15</mn></mrow> </math> ).</p><p><strong>Conclusions: </strong>We have developed a comprehensive imaging platform that integrates a single-photon wide-field navigation system with miniature two-photon and three-photon microscopy, leveraging the strengths of each modality. Building on this platform, we established a streamlined workflow tailored for imaging freely behaving animals, markedly expanding its applicability and improving efficiency.</p>","PeriodicalId":54335,"journal":{"name":"Neurophotonics","volume":"12 2","pages":"025018"},"PeriodicalIF":4.8000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12204226/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurophotonics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1117/1.NPh.12.2.025018","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/27 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Significance: Miniature multiphoton microscopy has revolutionized neuronal imaging in freely behaving animals. However, its shallow depth of field-a result of high axial resolution-combined with a limited field of view (FOV), makes it challenging for researchers to identify regions of interest in three-dimensional space across multimillimeter cranial windows, thereby reducing the system's ease of use.
Aim: We aimed to develop a multimodal imaging platform with enhanced guidance and a standardized workflow tailored for efficient imaging of freely behaving animals.
Approach: We present a wide-field fluorescence navigation system (WF-Nav) featuring a 90-mm working distance, a 4-mm FOV, and single-cell resolution, enabling rapid and precise localization of designated regions. By seamlessly integrating this navigation system with our prior miniature multiphoton microscopes, we established a multimodal platform that supports versatile imaging modalities and seamless transitions to two- or three-photon imaging. Building on this integration, we developed a streamlined workflow for efficient, user-friendly imaging in freely behaving mice.
Results: We validated the system through large-FOV imaging (4 mm), dual-color imaging (920 and 1030 nm), and deep-brain neuronal imaging (up to 1 mm) in either awake mice or freely moving mice. The entire experimental procedure was completed in , achieving a 100% success rate ( ).
Conclusions: We have developed a comprehensive imaging platform that integrates a single-photon wide-field navigation system with miniature two-photon and three-photon microscopy, leveraging the strengths of each modality. Building on this platform, we established a streamlined workflow tailored for imaging freely behaving animals, markedly expanding its applicability and improving efficiency.
期刊介绍:
At the interface of optics and neuroscience, Neurophotonics is a peer-reviewed journal that covers advances in optical technology applicable to study of the brain and their impact on the basic and clinical neuroscience applications.