Martino Nicola, Kwok Sheldon J J, Liapis Andreas C, Forward Sarah, Jang Hoon, Kim Hwi-Min, Wu Sarah J, Wu Jiamin, Dannenberg Paul H, Jang Sun-Joo, Lee Yong-Hee, Yun Seok-Hyun
Harvard Medical School and Wellman Center for Photomedicine, Massachusetts General Hospital, 50 Blossom Street, Boston, MA 02114, USA.
Harvard-MIT Health Sciences and Technology, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.
Nat Photonics. 2019 Oct;13(10):720-727. doi: 10.1038/s41566-019-0489-0. Epub 2019 Jul 22.
Large-scale single-cell analyses have become increasingly important given the role of cellular heterogeneity in complex biological systems. However, no current techniques enable optical imaging of uniquely-tagged individual cells. Fluorescence-based approaches can only distinguish a small number of distinct cells or cell groups at a time because of spectral crosstalk between conventional fluorophores. Here we investigate large-scale cell tracking using intracellular laser particles as imaging probes that emit coherent laser light with a characteristic wavelength. Made of silica-coated semiconductor microcavities, these laser particles have single-mode emission over a broad range from 1170 to 1580 nm with sub-nm linewidths, enabling massive spectral multiplexing. We explore the stability and biocompatibility of these probes in vitro and their utility for wavelength-multiplexed cell tagging and imaging. We demonstrate real-time tracking of thousands of individual cells in a 3D tumour model over several days showing different behavioural phenotypes.
鉴于细胞异质性在复杂生物系统中的作用,大规模单细胞分析变得越来越重要。然而,目前没有技术能够对唯一标记的单个细胞进行光学成像。基于荧光的方法由于传统荧光团之间的光谱串扰,一次只能区分少量不同的细胞或细胞群。在这里,我们研究使用细胞内激光粒子作为成像探针进行大规模细胞追踪,这些激光粒子发射具有特征波长的相干激光。这些激光粒子由二氧化硅包覆的半导体微腔制成,在1170至1580纳米的宽范围内具有单模发射,线宽小于1纳米,能够实现大规模光谱复用。我们探索了这些探针在体外的稳定性和生物相容性,以及它们在波长复用细胞标记和成像方面的实用性。我们展示了在三维肿瘤模型中对数千个单个细胞进行数天的实时追踪,显示出不同的行为表型。