Original Research: Label-free detection for radiation-induced apoptosis in glioblastoma cells. Issue 16 (October 2016)

• Record Type: Journal Article
• Authors: Qi, Dandan; Feng, Jingwen; Yang, Chengwen; Jin, Changrong; Sa, Yu; Feng, Yuanming
• Is Part Of: Experimental biology and medicine. Volume 241:Issue 16(2016)
• Page Start: 1751
• Page End: 1756
• Publication Date: 2016-10
• Subjects: Glioblastoma cell -- apoptosis -- cell morphology -- automatic feature extraction -- polarization diffraction imaging -- flow cytometry; Physiology -- Periodicals; Biology, Experimental -- Periodicals; Medicine, Experimental -- Periodicals; 610.72
• DOI: 10.1177/1535370216648024
• Languages: English
• ISSNs: 1535-3702

Abstract

Current flow cytometry (FCM) requires fluorescent dyes labeling cells which make the procedure costly and time consuming. This manuscript reports a feasibility study of detecting the cell apoptosis with a label-free method in glioblastoma cells. A human glioma cell line M059K was exposed to 8 Gy dose of radiation, which enables the cells to undergo radiation-induced apoptosis. The rates of apoptosis were studied at different time points post-irradiation with two different methods: FCM in combination with Annexin V-FITC/PI staining and a newly developed technique named polarization diffraction imaging flow cytometry. Totally 1000 diffraction images were acquired for each sample and the gray level co-occurrence matrix (GLCM) algorithm was used in morphological characterization of the apoptotic cells. Among the feature parameters extracted from each image pair, we found that the two GLCM parameters of angular second moment (ASM) and sum entropy (SumEnt) exhibit high sensitivities and consistencies as the apoptotic rates ( P a ) measured with FCM method. In addition, no significant difference exists between P a and ASM_S, P a and SumEnt_S, respectively ( P > 0.05). These results demonstrated that the new label-free method can detect cell apoptosis effectively. Cells can be directly used in the subsequent biochemical experiments as the structure and function of cells and biomolecules are well-preserved with this new method.