TY - JOUR
T1 - Post hoc Correction of Chromatic Aberrations in Large-Scale Volumetric Images in Confocal Microscopy
AU - Leiwe, Marcus N.
AU - Fujimoto, Satoshi
AU - Imai, Takeshi
N1 - Funding Information:
This work was supported by grants from AMED (JP20dm0207055 and JP21wm0525012 to TI), JST CREST program (JPMJCR2021 to TI), Grants-in-Aids from MEXT (JP16H06456 and JP21H00205 to TI), JSPS KAKENHI (JP17H06261 to TI; JP19K16261 and JP21K06411 to ML; and JP19K06886 to SF), and a grant from the Uehara Memorial Foundation (to TI).
Publisher Copyright:
Copyright © 2021 Leiwe, Fujimoto and Imai.
PY - 2021/12/10
Y1 - 2021/12/10
N2 - Over the last decade, tissue-clearing techniques have expanded the scale of volumetric fluorescence imaging of the brain, allowing for the comprehensive analysis of neuronal circuits at a millimeter scale. Multicolor imaging is particularly powerful for circuit tracing with fluorescence microscopy. However, multicolor imaging of large samples often suffers from chromatic aberration, where different excitation wavelengths of light have different focal points. In this study, we evaluated chromatic aberrations for representative objective lenses and a clearing agent with confocal microscopy and found that axial aberration is particularly problematic. Moreover, the axial chromatic aberrations were often depth-dependent. Therefore, we developed a program that is able to align depths for different fluorescence channels based on reference samples with fluorescent beads or data from guide stars within biological samples. We showed that this correction program can successfully correct chromatic aberrations found in confocal images of multicolor-labeled brain tissues. Our simple post hoc correction strategy is useful to obtain large-scale multicolor images of cleared tissues with minimal chromatic aberrations.
AB - Over the last decade, tissue-clearing techniques have expanded the scale of volumetric fluorescence imaging of the brain, allowing for the comprehensive analysis of neuronal circuits at a millimeter scale. Multicolor imaging is particularly powerful for circuit tracing with fluorescence microscopy. However, multicolor imaging of large samples often suffers from chromatic aberration, where different excitation wavelengths of light have different focal points. In this study, we evaluated chromatic aberrations for representative objective lenses and a clearing agent with confocal microscopy and found that axial aberration is particularly problematic. Moreover, the axial chromatic aberrations were often depth-dependent. Therefore, we developed a program that is able to align depths for different fluorescence channels based on reference samples with fluorescent beads or data from guide stars within biological samples. We showed that this correction program can successfully correct chromatic aberrations found in confocal images of multicolor-labeled brain tissues. Our simple post hoc correction strategy is useful to obtain large-scale multicolor images of cleared tissues with minimal chromatic aberrations.
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U2 - 10.3389/fnana.2021.760063
DO - 10.3389/fnana.2021.760063
M3 - Article
AN - SCOPUS:85121906936
SN - 1662-5129
VL - 15
JO - Frontiers in Neuroanatomy
JF - Frontiers in Neuroanatomy
M1 - 760063
ER -