Lee Ariel J, Yoon DongJo, Han SeungYun, Hugonnet Herve, Park WeiSun, Park Je-Kyun, Nam YoonKey, Park YongKeun
Department of Physics, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of Korea.
KAIST Institute for Health Science and Technology, KAIST, Daejeon 34141, Republic of Korea.
Biomed Opt Express. 2021 Oct 15;12(11):6928-6939. doi: 10.1364/BOE.439404. eCollection 2021 Nov 1.
The highly complex central nervous systems of mammals are often studied using three-dimensional (3D) primary neuronal cultures. A coupled confocal microscopy and immunofluorescence labeling are widely utilized for visualizing the 3D structures of neurons. However, this requires fixation of the neurons and is not suitable for monitoring an identical sample at multiple time points. Thus, we propose a label-free monitoring method for 3D neuronal growth based on refractive index tomograms obtained by optical diffraction tomography. The 3D morphology of the neurons was clearly visualized, and the developmental processes of neurite outgrowth in 3D spaces were analyzed for individual neurons.
哺乳动物高度复杂的中枢神经系统通常使用三维(3D)原代神经元培养物进行研究。共聚焦显微镜和免疫荧光标记相结合被广泛用于可视化神经元的三维结构。然而,这需要固定神经元,并且不适用于在多个时间点监测同一样本。因此,我们提出了一种基于光学衍射层析成像获得的折射率断层图的无标记3D神经元生长监测方法。清晰地可视化了神经元的三维形态,并对单个神经元在三维空间中的神经突生长发育过程进行了分析。