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Lensless imaging system to quantify cell proliferation

机译:无镜头成像系统可量化细胞增殖

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摘要

Owing to its simplicity, lensless imaging system is adept at continuous monitoring of adherent cells inside the incubator. The setup consists of a CMOS sensor with pixel pitch of 2.2 μm and field of view of 24 mm~2, LED with a dominating wavelength of 525 mn, along with a pinhole of 150 μm as the source of illumination. The in-line hologram obtained from cells depends on the degree of cell-substrate adhesion. Drastic difference is observed between the holographic patterns of floating and adherent cells. In addition, the well-established fact of reduction of cell-substrate contact during cell division is observed with our system based on corresponding spontaneous transition in the holographic pattern. Here, we demonstrate that by recognizing this specific holographic pattern, number of cells undergoing mitosis in a cell culture with a population of approximately 5000 cells, can be estimated in real-time. The method is assessed on comparison with Edu-based proliferation assay. The approach is straightforward and it eliminates the use of markers to estimate the proliferation rate of a given cell culture. Unlike most proliferation assays, the cells are not harvested enabling continuous monitoring of cell culture.
机译:由于其简单性,无透镜成像系统擅长于连续监测培养箱内贴壁细胞。该设置包括一个像素间距为2.2μm的CMOS传感器和24 mm〜2的视场,一个主波长为525 mn的LED以及一个150μm的针孔作为照明源。从细胞获得的在线全息图取决于细胞与基底的粘附程度。在浮动细胞和贴壁细胞的全息图案之间观察到巨大的差异。此外,我们的系统基于全息图案中相应的自发转变,观察到了公认的减少细胞分裂过程中细胞与底物接触的事实。在这里,我们证明了通过识别这种特定的全息图模式,可以实时估计大约有5000个细胞的细胞培养中经历有丝分裂的细胞数量。通过与基于Edu的增殖分析进行比较来评估该方法。该方法是直接的,并且消除了使用标记来估计给定细胞培养物的增殖速率。与大多数增殖试验不同,没有收获细胞,无法对细胞培养进行连续监控。

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