Lee Hyeon Jeong, Zhang Delong, Jiang Ying, Wu Xiangbing, Shih Pei-Yu, Liao Chien-Sheng, Bungart Brittani, Xu Xiao-Ming, Drenan Ryan, Bartlett Edward, Cheng Ji-Xin
Weldon School of Biomedical Engineering, Purdue University , West Lafayette, Indiana 47907-2032, United States.
Interdisciplinary Life Science Program, Purdue University , West Lafayette, Indiana 47907, United States.
J Phys Chem Lett. 2017 May 4;8(9):1932-1936. doi: 10.1021/acs.jpclett.7b00575. Epub 2017 Apr 17.
Detecting membrane potentials is critical for understanding how neuronal networks process information. We report a vibrational spectroscopic signature of neuronal membrane potentials identified through hyperspectral stimulated Raman scattering (SRS) imaging of patched primary neurons. High-speed SRS imaging allowed direct visualization of puff-induced depolarization of multiple neurons in mouse brain slices, confirmed by simultaneous calcium imaging. The observed signature, partially dependent on sodium ion influx, is interpreted as ion interactions on the CH Fermi resonance peak in proteins. By implementing a dual-SRS balanced detection scheme, we detected single action potentials in electrically stimulated neurons. These results collectively demonstrate the potential of sensing neuronal activities at multiple sites with a label-free vibrational microscope.
检测膜电位对于理解神经网络如何处理信息至关重要。我们报告了通过对膜片钳记录的原代神经元进行高光谱受激拉曼散射(SRS)成像识别出的神经元膜电位的振动光谱特征。高速SRS成像能够直接观察到小鼠脑片中多个神经元因微量压力喷射引起的去极化,同时进行的钙成像也证实了这一点。观察到的特征部分依赖于钠离子内流,被解释为蛋白质中CH费米共振峰上的离子相互作用。通过实施双SRS平衡检测方案,我们在电刺激的神经元中检测到了单个动作电位。这些结果共同证明了使用无标记振动显微镜在多个位点传感神经元活动的潜力。