Key Laboratory of Optoelectronic Devices and Systems of Ministry of Education and Guangdong Province, College of Optoelectronic Engineering, Shenzhen University, Shenzhen, China.
College of Physics and Energy, Shenzhen University, Shenzhen, China.
J Biophotonics. 2019 Jul;12(7):e201800420. doi: 10.1002/jbio.201800420. Epub 2019 Apr 14.
Astrocytes play a key role in the central nervous system. However, methods of visualizing astrocytes in the deep brain in vivo have been lacking. 3-photon fluorescence imaging of astrocytes labeled by sulforhodamine 101 (SR101) is demonstrated in deep mouse brain in vivo. Excitation wavelength selection was guided by wavelength-dependent 3-photon action cross section (ησ ) measurement of SR101. 3-photon fluorescence imaging of the SR101-labeled vasculature enabled an imaging depth of 1340-μm into the mouse brain. This justifies the deep imaging capability of the technique and indicates that the imaging depth is not determined by the signal-to-background ratio limit encountered in 2-photon fluorescence imaging. Visualization of astrocytes 910 μm below the surface of the mouse brain in vivo is demonstrated, 30% deeper than that using 2-photon fluorescence microscopy. Through quantitative comparison of the signal difference between the SR101-labeled blood vessels and astrocytes, the challenges of visualizing astrocytes below the white matter is further elucidated.
星形胶质细胞在中枢神经系统中发挥着关键作用。然而,在体内可视化深部脑星形胶质细胞的方法一直缺乏。本文展示了利用 sulforhodamine 101(SR101)标记的星形胶质细胞的三光子荧光成像在体内深部小鼠脑内的应用。激发波长的选择是通过对 SR101 的波长依赖性三光子作用截面(ησ)测量来指导的。对 SR101 标记的脉管系统的三光子荧光成像使成像深度达到 1340μm 进入小鼠大脑。这证明了该技术的深部成像能力,并表明成像深度不是由在双光子荧光成像中遇到的信号与背景比限制决定的。本文还证明了在体活鼠脑表面下 910μm 处星形胶质细胞的可视化,比使用双光子荧光显微镜深 30%。通过对 SR101 标记的血管和星形胶质细胞之间信号差异的定量比较,进一步阐明了在白质下方可视化星形胶质细胞所面临的挑战。