1.Institut Langevin, ESPCI Paris, PSL University, CNRS, 10 rue Vauquelin, Paris, France
2.Institut de la Vision, Sorbonne Université, INSERM, CNRS, F-75012 Paris, France
3.Quinze-Vingts National Eye Hospital, 28 Rue de Charenton, Paris 75012, France
4.Fondation Ophtalmologique Rothschild, F-75019 Paris, France
5.Department of Ophthalmology, The University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, United States
Kate Grieve (kategrieve@gmail.com)
纸质出版日期:2020,
网络出版日期:2020-08-17,
收稿日期:2019-12-09,
修回日期:2020-06-19,
录用日期:2020-07-27
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Dynamic full-field optical coherence tomography: 3D live-imaging of retinal organoids[J]. LSA, 2020,9(5):1306-1314.
Scholler, J. et al. Dynamic full-field optical coherence tomography: 3D live-imaging of retinal organoids. Light: Science & Applications, 9, 1306-1314 (2020).
Dynamic full-field optical coherence tomography: 3D live-imaging of retinal organoids[J]. LSA, 2020,9(5):1306-1314. DOI: 10.1038/s41377-020-00375-8.
Scholler, J. et al. Dynamic full-field optical coherence tomography: 3D live-imaging of retinal organoids. Light: Science & Applications, 9, 1306-1314 (2020). DOI: 10.1038/s41377-020-00375-8.
Optical coherence tomography offers astounding opportunities to image the complex structure of living tissue but lacks functional information. We present dynamic full-field optical coherence tomography as a technique to noninvasively image living human induced pluripotent stem cell-derived retinal organoids. Coloured images with an endogenous contrast linked to organelle motility are generated
with submicrometre spatial resolution and millisecond temporal resolution
creating a way to identify specific cell types in living tissue via their function.
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