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DOI: 10.3791/68529-v
Jimin Cho1, Mahn Jae Lee2, Juyeon Park3,4, Jaehyeok Lee5, Sumin Lee5, Chaeuk Chung2, Bon-Kyoung Koo6, YongKeun Park3,4,5
1Graduate School of Stem Cell and Regenerative Biology,Korea Advanced Institute of Science and Technology (KAIST), 2Division of Pulmonary and Allergy Medicine, Department of Internal Medicine,Chungnam National University Hospital, 3Department of Physics,KAIST, 4KAIST Institute for Health Science and Technology,KAIST, 5Tomocube Inc., 6Center for Genome Engineering,Institute for Basic Science
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This study presents a protocol for high-resolution, label-free, three-dimensional imaging of organoids, facilitating real-time visualization of structural dynamics and drug responses. The approach utilizes low-coherence holotomography, enhancing the ability to monitor biophysical changes during organoid development.
我们提出了一种使用低相干全息断层扫描对类器官进行高分辨率、无标记和三维成像的分步协议。该协议详细介绍了类器官培养制备、成像采集和计算图像分析,从而能够实时可视化活类器官中的结构动力学和药物反应。
我们的目标是建立一种实时、无标记的成像方法,以监测活类器官在开发过程中和对药物的反应的生物物理变化。该协议有助于简化活类器官的成像规模和非侵入性药物测试,并得到人工智能驱动的突变和生物医学研究的定量质地选择的支持。我们计划进一步整合无标记 3D 成像和一年分析,以在疾病建模和精准医学中进行高分辨率、非侵入性类器官研究。
首先,从含有细胞外基质的48孔板的每个孔中吸出用过的培养基。向每个孔中加入 200 微升细胞回收溶液,并在 4 摄氏度下孵育 30 分钟。使用移液器,轻轻收集类器官悬浮液并将其转移到微量离心管中。
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