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Wide-field fluorescence navigation system for efficient miniature multiphoton imaging in freely behaving animals

  • Runlong Wu*
  • , Yukun Sun
  • , Zeyu Hao
  • , Chunzhu Zhao
  • , Lishuang Feng
  • , Aimin Wang
  • , Heping Cheng
  • *Corresponding author for this work
  • Beijing Information Science & Technology University
  • Beijing Laboratory of Biomedical Imaging
  • Beihang University
  • Peking University

Research output: Contribution to journalArticlepeer-review

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 ∼20 min, achieving a 100% success rate (n ¼ 15). 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.

Original languageEnglish
Article number025018
JournalNeurophotonics
Volume12
Issue number2
DOIs
StatePublished - 1 Apr 2025

Keywords

  • freely behaving animals
  • miniature three-photon microscope
  • miniature two-photon microscope
  • neuronal imaging
  • neurophotonics
  • wide-field fluorescence microscope

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