TY - GEN
T1 - High-speed super-multiplex imaging of brain tissue
AU - Oda, Robert
AU - Shou, Jingwen
AU - Karasawa, Keiko
AU - Nuriya, Mutsuo
AU - Yasui, Masato
AU - Ozeki, Yasuyuki
N1 - Funding Information:
This work is supported by JST CREST Grant Number JPMJCR1872, Japan, JSPS KAKENHI Grant Number JP19J22546, JP20H02650, JP20H05725, and JP18K18847, Japan. R.O. is supported by Crown Prince Akihito Scholarship Foundation. J.S. is supported by International Research Fellow of the Japan Society for the Promotion of Science.
Publisher Copyright:
© 2021 SPIE. All rights reserved.
PY - 2021
Y1 - 2021
N2 - Cells within the brain are highly organized and coordinate complex processes with each other. The ability to simultaneously visualize the organization and interactions of cells and molecules within brain tissue remains an important issue to understand the brain comprehensively. Stimulated Raman scattering (SRS) and fluorescence, two powerful imaging modalities, can provide complementary molecular contrasts within cells and tissue samples. Here, we present a high-speed super-multiplex imaging platform that combines SRS microscopy with confocal fluorescence microscopy to perform rapid 7-color brain imaging. We show simultaneous imaging of cellular components within the brain such as astrocytes, axons, and blood vessels while also showing organelles such as the nucleus and actin cytoskeleton. Also, we demonstrate the ability to take depth-resolved images that elucidate the three-dimensional organization of diverse components within brain tissue. This platform can be adapted to explore various processes within brain tissue that can reveal critical information about the brain and how it is affected by diseases, which leads toward a deeper understanding of disease progression and potentially the development of therapeutic options for brain diseases.
AB - Cells within the brain are highly organized and coordinate complex processes with each other. The ability to simultaneously visualize the organization and interactions of cells and molecules within brain tissue remains an important issue to understand the brain comprehensively. Stimulated Raman scattering (SRS) and fluorescence, two powerful imaging modalities, can provide complementary molecular contrasts within cells and tissue samples. Here, we present a high-speed super-multiplex imaging platform that combines SRS microscopy with confocal fluorescence microscopy to perform rapid 7-color brain imaging. We show simultaneous imaging of cellular components within the brain such as astrocytes, axons, and blood vessels while also showing organelles such as the nucleus and actin cytoskeleton. Also, we demonstrate the ability to take depth-resolved images that elucidate the three-dimensional organization of diverse components within brain tissue. This platform can be adapted to explore various processes within brain tissue that can reveal critical information about the brain and how it is affected by diseases, which leads toward a deeper understanding of disease progression and potentially the development of therapeutic options for brain diseases.
KW - Neuroimaging
KW - Stimulated Raman scattering microscopy
KW - Super multiplex
UR - http://www.scopus.com/inward/record.url?scp=85108527515&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85108527515&partnerID=8YFLogxK
U2 - 10.1117/12.2577346
DO - 10.1117/12.2577346
M3 - Conference contribution
AN - SCOPUS:85108527515
T3 - Progress in Biomedical Optics and Imaging - Proceedings of SPIE
BT - Advanced Chemical Microscopy for Life Science and Translational Medicine 2021
A2 - Cheng, Ji-Xin
A2 - Min, Wei
A2 - Simpson, Garth J.
PB - SPIE
T2 - Advanced Chemical Microscopy for Life Science and Translational Medicine 2021
Y2 - 6 March 2021 through 11 March 2021
ER -