Department of Physics, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea; KAIST Institute for Health Science and Technology, Daejeon, Republic of Korea
Young-Ho Lee
Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea; Curocell Inc, Daejeon, Republic of Korea
Jinyeop Song
Department of Physics, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea; KAIST Institute for Health Science and Technology, Daejeon, Republic of Korea
Geon Kim
Department of Physics, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea; KAIST Institute for Health Science and Technology, Daejeon, Republic of Korea
YoungJu Jo
Department of Physics, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea; KAIST Institute for Health Science and Technology, Daejeon, Republic of Korea
HyunSeok Min
Tomocube Inc, Daejeon, Republic of Korea
Chan Hyuk Kim
Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea
Department of Physics, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea; KAIST Institute for Health Science and Technology, Daejeon, Republic of Korea
The immunological synapse (IS) is a cell-cell junction between a T cell and a professional antigen-presenting cell. Since the IS formation is a critical step for the initiation of an antigen-specific immune response, various live-cell imaging techniques, most of which rely on fluorescence microscopy, have been used to study the dynamics of IS. However, the inherent limitations associated with the fluorescence-based imaging, such as photo-bleaching and photo-toxicity, prevent the long-term assessment of dynamic changes of IS with high frequency. Here, we propose and experimentally validate a label-free, volumetric, and automated assessment method for IS dynamics using a combinational approach of optical diffraction tomography and deep learning-based segmentation. The proposed method enables an automatic and quantitative spatiotemporal analysis of IS kinetics of morphological and biochemical parameters associated with IS dynamics, providing a new option for immunological research.