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Lensless imaging system to quantify cell proliferation

机译:透镜成像系统量化细胞增殖

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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 mm2, LED with a dominating wavelength of 525 nm, 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,无透镜成像系统熟练地在培养箱内连续监测粘附细胞。该设置包括一个CMOS传感器,其像素间距为2.2μm的像素间距和24 mm2的视场,具有525nm的主导波长的LED,以及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基板粘附程度。在浮动和粘附细胞的全息模式之间观察到剧烈差异。此外,通过基于全息图案中的相应的自发转变,观察到细胞分裂期间细胞分裂期间降低细胞基板接触的良好事实。这里,我们证明通过识别这种特定的全息模式,可以实时估计具有约5000个细胞的细胞培养物中经历有丝分裂的细胞数。与基于EDU的增殖测定相比评估该方法。该方法是简单的,并且消除了标记物的使用来估计给定细胞培养的增殖速率。与大多数增殖测定不同,细胞未收获,从而能够连续监测细胞培养物。

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