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Double-helix optical point spread function enables real-time mesoscopic 3D functional microangiography in the living mouse brain and skull

  • Baoyuan Zhang
  • , Shiyao Guo
  • , Lin Tang
  • , Yi Chen
  • , Lukas Glandorf
  • , Etienne Jessen
  • , Xuyang Chang
  • , Tian Jin
  • , Michael Reiss
  • , Shuxin Lyu
  • , Qiang Fu
  • , Hadi Amata
  • , Wolfgang Heidrich
  • , Chaim Glück
  • , Dominik Schillinger
  • , Bruno Weber
  • , Xosé Luís Deán-Ben
  • , Weibo Wang*
  • , Xiong Dun*
  • , Daniel Razansky*
  • Zhenyue Chen*, Quanyu Zhou*
*Corresponding author for this work
  • University of Zurich
  • Harbin Institute of Technology
  • Tongji University
  • Technische Universität Darmstadt
  • King Abdullah University of Science and Technology

Research output: Contribution to journalArticlepeer-review

Abstract

Quantitative, volumetric imaging of cerebrovascular networks and microcirculation is essential for understanding brain function. However, rapid mesoscopic 3D imaging remains challenging because of fundamental trade-offs between spatiotemporal resolution, field of view, and sensitivity to functional parameters. Here we present a mesoscopic fluorescence imaging platform featuring a double-helix phase mask for real-time, depth-resolved measurements through the intact mouse skull. The compact phase-mask design is compatible with both laser-scanning and widefield microscopy. Using multifocal laser scanning, we demonstrate real-time volumetric in vivo imaging while discriminating calvarial from cerebral vasculature across 6.6×6.6×0.8 mm3 volume. Beyond high-resolution structural imaging, perfusion time-to-peak values are extracted from the laser-scanning configuration while accurate flow velocity/direction information is provided via widefield tracking of fluorescently labeled cells. We demonstrate the platform’s capabilities by analyzing brain-layer-specific perfusion dynamics and vascular topology in glioma-bearing mouse brains, offering unprecedented views for probing cerebrovascular alterations in both physiological and pathological contexts.

Original languageEnglish
Article number5167
JournalNature Communications
Volume17
Issue number1
DOIs
StatePublished - Dec 2026

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