110 μm thin endo-microscope for deep-brain in vivo observations of neuronal connectivity, activity and blood flow dynamics

被引:66
作者
Stiburek, Miroslav [1 ]
Ondrackova, Petra [1 ]
Tuckova, Tereza [1 ]
Turtaev, Sergey [2 ]
Siler, Martin [1 ]
Pikalek, Tomas [1 ]
Jakl, Petr [1 ]
Gomes, Andre [2 ]
Krejci, Jana [3 ]
Kolbabkova, Petra [1 ]
Uhlirova, Hana [1 ]
Cizmar, Tomas [1 ,2 ,4 ]
机构
[1] Czech Acad Sci, Inst Sci Instruments, Kralovopolska 147, Brno 61264, Czech Republic
[2] Leibniz Inst Photon Technol, Albert Einstein Str 9, D-07745 Jena, Germany
[3] Czech Acad Sci, Inst Biophys, Kralovopolska 135, Brno 61265, Czech Republic
[4] Friedrich Schiller Univ Jena, Inst Appl Opt, Frobelstieg 1, D-07743 Jena, Germany
基金
欧盟地平线“2020”; 欧洲研究理事会;
关键词
HIGH-RESOLUTION; FOCUSING LIGHT; MULTIMODE; FLUCTUATIONS; TISSUE;
D O I
10.1038/s41467-023-36889-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Controlled light transport through multimode fibres has recently emerged as uniquely atraumatic prospect to study deep brain structures. Here, authors present hair-thin endoscope providing detailed view through the whole depth of living animal brain. Light-based in-vivo brain imaging relies on light transport over large distances of highly scattering tissues. Scattering gradually reduces imaging contrast and resolution, making it difficult to reach structures at greater depths even with the use of multiphoton techniques. To reach deeper, minimally invasive endo-microscopy techniques have been established. These most commonly exploit graded-index rod lenses and enable a variety of modalities in head-fixed and freely moving animals. A recently proposed alternative is the use of holographic control of light transport through multimode optical fibres promising much less traumatic application and superior imaging performance. We present a 110 mu m thin laser-scanning endo-microscope based on this prospect, enabling in-vivo volumetric imaging throughout the whole depth of the mouse brain. The instrument is equipped with multi-wavelength detection and three-dimensional random access options, and it performs at lateral resolution below 1 mu m. We showcase various modes of its application through the observations of fluorescently labelled neurones, their processes and blood vessels. Finally, we demonstrate how to exploit the instrument to monitor calcium signalling of neurones and to measure blood flow velocity in individual vessels at high speeds.
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页数:9
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