TY - JOUR
T1 - biPACT
T2 - A method for three-dimensional visualization of mouse spinal cord circuits of long segments with high resolution
AU - Nakanishi, Katsuyuki
AU - Shinozaki, Munehisa
AU - Nagoshi, Narihito
AU - Nakamura, Masaya
AU - Okano, Hideyuki
N1 - Funding Information:
We appreciate the assistance provided by S. Shibata, J. Koyama, S. Nori, O. Tsuji, K. Sugai, and S. Kawashima, all of whom are members of the spinal cord research team in the Department of Orthopedic Surgery and Physiology, Keio University School of Medicine, Tokyo, Japan. This work was supported by the Japan Agency for Medical Research and Development (AMED; grant nos. JP15bm0204001 and JP20bk0104114 to H.O. and M.N.), and the General Insurance Association of Japan Medical Research Grant to K.N and M.S.
Funding Information:
M.N. declares a consultancy role with K-Pharma Inc. and research funding from RMic and Hisamitsu. H.O. declares a leadership position at Keio University School of Medicine and is a compensated scientific consultant for San Bio Co. Ltd. and K Pharma Inc. These companies have no relationship with the present study. The other authors declare no competing interest.
Funding Information:
We appreciate the assistance provided by S. Shibata, J. Koyama, S. Nori, O. Tsuji, K. Sugai, and S. Kawashima, all of whom are members of the spinal cord research team in the Department of Orthopedic Surgery and Physiology, Keio University School of Medicine, Tokyo, Japan. This work was supported by the Japan Agency for Medical Research and Development (AMED; grant nos. JP15bm0204001 and JP20bk0104114 to H.O. and M.N.), and the General Insurance Association of Japan Medical Research Grant to K.N and M.S.
Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/9/1
Y1 - 2022/9/1
N2 - Background: The spatial complexity of neuronal circuits in the central nervous system is a hurdle in understanding and treating brain and spinal cord injury (SCI). Although several methods have recently been developed to render the spinal cord transparent and label specific neural circuits, three-dimensional visualization of long segments of spinal cord with high resolution remains challenging for SCI researchers. New Method: We present a method that combines tissue staining of neuronal tracts traced with biotinylated dextran amine (BDA) and a modified passive clarity clearing protocol to describe individual fibers in long segments of mouse spinal cord. Results: Corticospinal tract was traced with BDA with a mouse model of thoracic spinal cord injury. The spinal cord was stained and cleared in two weeks with four solutions: staining solution, hydrogel solution, clearing solution, and observation solution. The samples were observed with a light-sheet microscope, and three-dimensional reconstruction was performed with ImageJ software. High resolution-images comparable with tissue sections were obtained continuously and circumferentially. By tiling, it was possible to obtain high-resolution images of long segments of the spinal cord. The tissue could be easily re-stained in case of fading. Comparison with existing methods: The present method does not require special equipment such as vacuum devices, can label specific circuits without genetic technology, and re-staining rounds can be easily implemented. Conclusions: By using simple neural staining and clearing methods, it was possible to acquire a wide range of high-resolution three-dimensional images of the spinal cord.
AB - Background: The spatial complexity of neuronal circuits in the central nervous system is a hurdle in understanding and treating brain and spinal cord injury (SCI). Although several methods have recently been developed to render the spinal cord transparent and label specific neural circuits, three-dimensional visualization of long segments of spinal cord with high resolution remains challenging for SCI researchers. New Method: We present a method that combines tissue staining of neuronal tracts traced with biotinylated dextran amine (BDA) and a modified passive clarity clearing protocol to describe individual fibers in long segments of mouse spinal cord. Results: Corticospinal tract was traced with BDA with a mouse model of thoracic spinal cord injury. The spinal cord was stained and cleared in two weeks with four solutions: staining solution, hydrogel solution, clearing solution, and observation solution. The samples were observed with a light-sheet microscope, and three-dimensional reconstruction was performed with ImageJ software. High resolution-images comparable with tissue sections were obtained continuously and circumferentially. By tiling, it was possible to obtain high-resolution images of long segments of the spinal cord. The tissue could be easily re-stained in case of fading. Comparison with existing methods: The present method does not require special equipment such as vacuum devices, can label specific circuits without genetic technology, and re-staining rounds can be easily implemented. Conclusions: By using simple neural staining and clearing methods, it was possible to acquire a wide range of high-resolution three-dimensional images of the spinal cord.
KW - Light-sheet microscope
KW - Spinal cord injury
KW - Three dimensional observation
KW - Tracing
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U2 - 10.1016/j.jneumeth.2022.109672
DO - 10.1016/j.jneumeth.2022.109672
M3 - Article
C2 - 35843371
AN - SCOPUS:85134807716
SN - 0165-0270
VL - 379
JO - Journal of Neuroscience Methods
JF - Journal of Neuroscience Methods
M1 - 109672
ER -