Literature DB >> 29649479

A spherical aberration-free microscopy system for live brain imaging.

Yoshihiro Ue1, Hiromu Monai2, Kaori Higuchi1, Daisuke Nishiwaki1, Tetsuya Tajima1, Kenya Okazaki1, Hiroshi Hama3, Hajime Hirase3, Atsushi Miyawaki4.   

Abstract

The high-resolution in vivo imaging of mouse brain for quantitative analysis of fine structures, such as dendritic spines, requires objectives with high numerical apertures (NAs) and long working distances (WDs). However, this imaging approach is often hampered by spherical aberration (SA) that results from the mismatch of refractive indices in the optical path and becomes more severe with increasing depth of target from the brain surface. Whereas a revolving objective correction collar has been designed to compensate SA, its adjustment requires manual operation and is inevitably accompanied by considerable focal shift, making it difficult to acquire the best image of a given fluorescent object. To solve the problems, we have created an objective-attached device and formulated a fast iterative algorithm for the realization of an automatic SA compensation system. The device coordinates the collar rotation and the Z-position of an objective, enabling correction collar adjustment while stably focusing on a target. The algorithm provides the best adjustment on the basis of the calculated contrast of acquired images. Together, they enable the system to compensate SA at a given depth. As proof of concept, we applied the SA compensation system to in vivo two-photon imaging with a 25 × water-immersion objective (NA, 1.05; WD, 2 mm). It effectively reduced SA regardless of location, allowing quantitative and reproducible analysis of fine structures of YFP-labeled neurons in the mouse cerebral cortical layers. Interestingly, although the cortical structure was optically heterogeneous along the z-axis, the refractive index of each layer could be assessed on the basis of the compensation degree. It was also possible to make fully corrected three-dimensional reconstructions of YFP-labeled neurons in live brain samples. Our SA compensation system, called Deep-C, is expected to bring out the best in all correction-collar-equipped objectives for imaging deep regions of heterogeneous tissues.
Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cerebral cortex; Dendritic spine; Refractive index; Spherical aberration; Two-photon microscopy

Mesh:

Year:  2018        PMID: 29649479     DOI: 10.1016/j.bbrc.2018.04.049

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  3 in total

1.  Pathological application of carbocyanine dye-based multicolour imaging of vasculature and associated structures.

Authors:  Alu Konno; Naoya Matsumoto; Yasuko Tomono; Shigetoshi Okazaki
Journal:  Sci Rep       Date:  2020-07-28       Impact factor: 4.379

2.  Adaptive Optical Two-Photon Microscopy for Surface-Profiled Living Biological Specimens.

Authors:  Kazushi Yamaguchi; Kohei Otomo; Yuichi Kozawa; Motosuke Tsutsumi; Tomoko Inose; Kenji Hirai; Shunichi Sato; Tomomi Nemoto; Hiroshi Uji-I
Journal:  ACS Omega       Date:  2020-11-30

3.  Complex-Amplitude-Modulation Vectorial Excitation Beam for High-Resolution Observation of Deep Regions in Two-Photon Microscopy.

Authors:  Naoya Matsumoto; Koyo Watanabe; Alu Konno; Takashi Inoue; Shigetoshi Okazaki
Journal:  Front Neurosci       Date:  2022-04-19       Impact factor: 5.152

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.