论文标题
具有计算特异性(PIC)的相成像,用于测量亚细胞隔室的干质量变化
Phase Imaging with Computational Specificity (PICS) for measuring dry mass changes in sub-cellular compartments
论文作者
论文摘要
由于其特异性,荧光显微镜(FM)已成为细胞生物学中的典型成像工具。但是,光漂白,光毒性和相关的工件继续限制FM的效用。最近,已经表明人工智能(AI)可以将一种形式的对比转换为另一种形式。我们提供图片,即定量相成像和AI的组合,该图片提供了具有高特异性的未标记的活细胞的信息。我们的成像系统允许自动培训,同时推理在采集软件中并实时运行。将计算的荧光图应用回QPI数据,我们多天独立地独立地测量了核和细胞质的生长,而不会丧失生存能力。使用抑制多个散射的QPI方法,我们测量了球体内单个细胞核的干质量含量。在目前的实施中,图片提供了一种多功能定量技术,用于在需要长期无标签成像的生物学应用中连续同时监测单个细胞成分。
Due to its specificity, fluorescence microscopy (FM) has become a quintessential imaging tool in cell biology. However, photobleaching, phototoxicity, and related artifacts continue to limit FM's utility. Recently, it has been shown that artificial intelligence (AI) can transform one form of contrast into another. We present PICS, a combination of quantitative phase imaging and AI, which provides information about unlabeled live cells with high specificity. Our imaging system allows for automatic training, while inference is built into the acquisition software and runs in real-time. Applying the computed fluorescence maps back to the QPI data, we measured the growth of both nuclei and cytoplasm independently, over many days, without loss of viability. Using a QPI method that suppresses multiple scattering, we measured the dry mass content of individual cell nuclei within spheroids. In its current implementation, PICS offers a versatile quantitative technique for continuous simultaneous monitoring of individual cellular components in biological applications where long-term label-free imaging is desirable.