TY - JOUR
T1 - Characterization of Intra/Extracellular Water States Probed by Ultrabroadband Multiplex Coherent Anti-Stokes Raman Scattering (CARS) Spectroscopic Imaging
AU - Nuriya, Mutsuo
AU - Yoneyama, Hiroaki
AU - Takahashi, Kyosuke
AU - Leproux, Philippe
AU - Couderc, Vincent
AU - Yasui, Masato
AU - Kano, Hideaki
N1 - Funding Information:
This work was supported by JSPS KAKENHI (26282117, 18H02000, and 18K18444 to H.K. and 16K07065 and ResonanceBio 16H01434 to M.N.) and JST PRESTO (JPMJPR17G6 to M.N.). The authors gratefully acknowledge J. Ukon, Ukon Craft Science, Ltd., for assisting with a fruitful collaboration between Japanese and French laboratories, T. Yamada for her help in maintaining the CHO cells, and Y. Koyama for his help in writing the MATLAB analysis program. Finally, the authors greatly acknowledge D. Kojic for helpful discussions and careful reading of the manuscript.
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/5/2
Y1 - 2019/5/2
N2 - Detailed knowledge of the water status in living organisms is crucial for understanding their physiology and pathophysiology. Here, we developed a technique to spectroscopically image water at high resolution using ultrabroadband multiplex coherent anti-Stokes Raman scattering (CARS) microscopy equipped with a supercontinuum light source. This system allows for the visualization of a wide spectrum of CARS signals from the fingerprint to the end of O-H stretching at a spectral resolution of ∼10 cm -1 . Application of the system to living mammalian cells revealed a spectral red shift of the O-H stretching vibrational band inside compared to outside the cells, suggesting the existence of stronger hydrogen bonds inside the cells. Furthermore, potential changes in spectra were examined by adding mannitol to the extracellular solution, which increases the osmolality outside the cells and thereby induces dehydration of the cells. Under this treatment, the red shift of the O-H stretching band was further enhanced, revealing the effects of mannitol on water states inside the cells. The methodology developed here should serve as a powerful tool for the chemical imaging of water in living cells in various biological and medical contexts.
AB - Detailed knowledge of the water status in living organisms is crucial for understanding their physiology and pathophysiology. Here, we developed a technique to spectroscopically image water at high resolution using ultrabroadband multiplex coherent anti-Stokes Raman scattering (CARS) microscopy equipped with a supercontinuum light source. This system allows for the visualization of a wide spectrum of CARS signals from the fingerprint to the end of O-H stretching at a spectral resolution of ∼10 cm -1 . Application of the system to living mammalian cells revealed a spectral red shift of the O-H stretching vibrational band inside compared to outside the cells, suggesting the existence of stronger hydrogen bonds inside the cells. Furthermore, potential changes in spectra were examined by adding mannitol to the extracellular solution, which increases the osmolality outside the cells and thereby induces dehydration of the cells. Under this treatment, the red shift of the O-H stretching band was further enhanced, revealing the effects of mannitol on water states inside the cells. The methodology developed here should serve as a powerful tool for the chemical imaging of water in living cells in various biological and medical contexts.
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U2 - 10.1021/acs.jpca.9b03018
DO - 10.1021/acs.jpca.9b03018
M3 - Article
C2 - 30957999
AN - SCOPUS:85065095776
SN - 1089-5639
VL - 123
SP - 3928
EP - 3934
JO - Journal of Physical Chemistry A
JF - Journal of Physical Chemistry A
IS - 17
ER -