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Measurements on ATP induced cellular fluctuations using real-time dual view transport of intensity phase microscopy

机译:使用强度相显微镜的实时双向传输技术测量ATP诱导的细胞波动

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摘要

Dual view transport of intensity phase microscopy is adopted to quantitatively study the regulation of adenosine triphosphate (ATP) on cellular mechanics. It extracts cell phases in real time from simultaneously captured under- and over-focus images. By computing the root-mean-square phase and correlation time, it is found that the cellular fluctuation amplitude and speed increased with ATP compared to those with ATP depletion. Besides, when adenylyl-imidodiphosphate (AMP-PNP) was introduced, it competed with ATP to bind to the ATP binding site, and the cellular fluctuation amplitude and speed decreased. The results prove that ATP is a factor in the regulation of cellular mechanics. To our best knowledge, it is the first time that the dual view transport of intensity phase microscopy was used for live cell phase imaging and analysis. Our work not only provides direct measurements on cellular fluctuations to study ATP regulation on cellular mechanics, but it also proves that our proposed dual view transport of intensity phase microscopy can be well used, especially in quantitative phase imaging of live cells in biological and medical applications.
机译:采用强度相显微镜的双向传输技术定量研究了三磷酸腺苷(ATP)对细胞力学的调节作用。它从同时捕获的聚焦不足和聚焦图像中实时提取细胞相。通过计算均方根相位和相关时间,发现与ATP消耗相比,ATP引起的细胞波动幅度和速度增加。此外,当引入腺苷酰亚氨基二磷酸(AMP-PNP)时,它与ATP竞争结合到ATP结合位点,细胞波动幅度和速度降低。结果证明,ATP是调节细胞力学的一个因素。据我们所知,这是首次将强度相显微镜的双向传输用于活细胞相成像和分析。我们的工作不仅可以直接测量细胞波动,以研究ATP对细胞力学的调控,还可以证明我们提出的强度相显微镜的双向传输可以很好地使用,特别是在生物和医学应用中活细胞的定量相成像中。

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