Dipartimento di Fisica, Politecnico di Milano, Piazza Leonardo da Vinci, 32, Milano, 20133, Italy.
Istituto di Fotonica e Nanotecnologie, Consiglio Nazionale delle Ricerche, Piazza Leonardo da Vinci, 32, Milano, 20133, Italy.
Lab Chip. 2023 Dec 20;24(1):34-46. doi: 10.1039/d3lc00639e.
Heterogeneity investigation at the single-cell level reveals morphological and phenotypic characteristics in cell populations. In clinical research, heterogeneity has important implications in the correct detection and interpretation of prognostic markers and in the analysis of patient-derived material. Among single-cell analysis, imaging flow cytometry allows combining information retrieved by single cell images with the throughput of fluidic platforms. Nevertheless, these techniques might fail in a comprehensive heterogeneity evaluation because of limited image resolution and bidimensional analysis. Light sheet fluorescence microscopy opened new ways to study in 3D the complexity of cellular functionality in samples ranging from single-cells to micro-tissues, with remarkably fast acquisition and low photo-toxicity. In addition, structured illumination microscopy has been applied to single-cell studies enhancing the resolution of imaging beyond the conventional diffraction limit. The combination of these techniques in a microfluidic environment, which permits automatic sample delivery and translation, would allow exhaustive investigation of cellular heterogeneity with high throughput image acquisition at high resolution. Here we propose an integrated optofluidic platform capable of performing structured light sheet imaging flow cytometry (SLS-IFC). The system encompasses a multicolor directional coupler equipped with a thermo-optic phase shifter, cylindrical lenses and a microfluidic network to generate and shift a patterned light sheet within a microchannel. The absence of moving parts allows a stable alignment and an automated fluorescence signal acquisition during the sample flow. The platform enables 3D imaging of an entire cell in about 1 s with a resolution enhancement capable of revealing sub-cellular features and sub-diffraction limit details.
单细胞水平的异质性研究揭示了细胞群体的形态和表型特征。在临床研究中,异质性对正确检测和解释预后标志物以及分析患者来源材料具有重要意义。在单细胞分析中,成像流式细胞术允许将单细胞图像获取的信息与流体平台的高通量相结合。然而,由于有限的图像分辨率和二维分析,这些技术可能无法全面评估异质性。光片荧光显微镜为研究单细胞到微组织样本中细胞功能的复杂性开辟了新途径,具有显著的快速采集和低光毒性。此外,结构光照明显微镜已应用于单细胞研究,将成像分辨率提高到超过传统衍射极限。将这些技术结合在微流控环境中,自动进行样品输送和转换,将允许以高通量采集高分辨率图像的方式,对细胞异质性进行详尽的研究。在这里,我们提出了一种集成的光流控平台,能够进行结构光片成像流式细胞术(SLS-IFC)。该系统包括一个多色定向耦合器,配备了热光相移器、柱面透镜和微流控网络,用于在微通道内产生和移动模式化的光片。由于没有移动部件,因此可以在样品流动过程中实现稳定的对准和自动荧光信号采集。该平台能够在大约 1 秒内对整个细胞进行 3D 成像,分辨率增强后能够揭示亚细胞特征和亚衍射极限细节。