Barkur Surekha, Bankapur Aseefhali, Pradhan Madhura, Chidangil Santhosh, Mathur Deepak, Ladiwala Uma
Manipal University, Department of Atomic and Molecular Physics, Manipal 576 104, India.
UM-DAE Centre for Excellence in Basic Sciences, Kalina Campus, Mumbai 400 098, India.
J Biomed Opt. 2015 Aug;20(8):85001. doi: 10.1117/1.JBO.20.8.085001.
Single-cell micro-Raman spectroscopy has been applied to explore cell differentiation in single, live, and malignant cells from two tumor cell lines. The spectra of differentiated cells exhibit substantial enhancement primarily in the intensities of protein peaks with concomitant decrease in intensities of O−P−O asymmetric stretching peaks in DNA/RNA. Principal component analyses show that the spectral score of differentiated cells tends to asymptotically approach that of spectra obtained from normal neural stem cells/progenitors. This lends credence to the notion that the observed spectral changes are specific to differentiation, since upon differentiation, malignant cells become less malignant and tend toward benignity.
单细胞显微拉曼光谱已被用于探索来自两种肿瘤细胞系的单个、活的恶性细胞的细胞分化。分化细胞的光谱主要在蛋白质峰强度上有显著增强,同时DNA/RNA中O−P−O不对称拉伸峰的强度降低。主成分分析表明,分化细胞的光谱得分趋于渐近地接近从正常神经干细胞/祖细胞获得的光谱得分。这支持了这样一种观点,即观察到的光谱变化是分化特有的,因为在分化时,恶性细胞的恶性程度降低并趋于良性。