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Isotropic, aberration-corrected light sheet microscopy for rapid high-resolution imaging of cleared tissue

Mostafa Aakhte*, Gesine F. Müller, Lennart Roos, Joe Li, Torben Göpel, Kurt R. Weiss, Aleyna M. Diniz, Jan Wenzel, Markus Schwaninger, Tobias Moser, Jan Huisken*

*Korrespondierende/r Autor/-in für diese Arbeit

Abstract

Light-sheet microscopy is ideal for imaging large and cleared tissues, but achieving a high isotropic resolution for a centimeter-sized sample is limited by slow and often aberrated, axially scanned light sheets. Here, we introduce a compact, high-speed light-sheet fluorescence microscope achieving 850 nm isotropic resolution across cleared samples up to 1 cm³ and refractive indices ranging from 1.33 to 1.56. Using off-the-shelf optics, we combine an air objective and a meniscus lens with an axially swept light sheet to achieve diffraction-limited resolution and aberration correction. The effective field of view is increased by twofold by correcting the field curvature of the light sheet using a concave mirror in the remote focusing unit. Adapting the light sheet’s motion with a closed-loop feedback enhances the imaging speed by tenfold, reaching 100 frames per second while maintaining resolution and field of view. We benchmark the system performance across scales, from subcellular structure up to centimeter scale, using various clearing methods.

OriginalspracheEnglisch
ZeitschriftNature Biotechnology
ISSN1087-0156
DOIs
PublikationsstatusAngenommen/Im Druck - 2025

Fördermittel

We thank C. Schmidt and his team at the central mechanical workshop of the Department of Physics at the University of Göttingen for their invaluable assistance in creating mechanical components. We also acknowledge K. Adner for several electronic components, P. Maier for his constructive input on the microscope development and T. Quilitz for her feedback on imaging mouse cochlea. We thank R. Fiolka and K. Dean for their insightful discussions on selecting the voice coil. We thank P. Lenart, M. A. Eskandari and R. Tsukanov for providing the Hamamatsu camera and frame grabber. We thank B. Lembrich and Z. S. Gilani, both from Lübeck, as well as I. Preuss and S. Langer of the Göttingen InnerEarLab for their expert technical support and B. Wolf and J. Neef for scientific discussion. We further acknowledge funding by the Alexander von Humboldt Foundation (J.H.; AvH professorship, including T.G.'s position) and the German Center for Cardiovascular Research (DZHK; 81X2300302) on behalf of M.A., J.W. and J.H. M.A., G.F.M., J.H. and T.M. are supported by the MWK (Niedersächsisches Ministerium für Wissenschaft und Kultur). We further acknowledge the support by the German Research Foundation via the Cluster of Excellence Multiscale Bioimaging (MBExC; EXC 2067/1-390729940) and its Hertha Sponer College at the University of Göttingen (M.A., G.F.M., L.R., A.M.D., T.M. and J.H.) as well as the collaborative research center 889 (L.R.). The work was additionally funded by the Else Kröner Fresenius Foundation through the Else Kröner Fresenius Center for Optogenetic Therapies (to J.H. and T.M.), European Union (ERC, ‘DynaHear,’ grant agreement no. 101054467), and the Fondation Pour l’Audition (FPA RD-2020-10) to T.M. The mouse brain experiments were supported by a grant from the Deutsche Forschungsgemeinschaft to J.W. (WE 6456/1-1).

TrägerTrägernummer
Else Kröner-Fresenius-Stiftung
Hertha Sponer College at the University of Göttingen
AvH professorship
European Commission
MWK
Niedersächsisches Ministerium für Wissenschaft und Kultur
Alexander von Humboldt Stiftung
Deutsche ForschungsgemeinschaftWE 6456/1-1, EXC 2067/1-390729940
European Research Council101054467
Fondation Pour l'AuditionFPA RD-2020-10
Deutsches Zentrum für Herz-Kreislaufforschung81X2300302

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