Mean frequency and relative fluorescence intensity measurement of γ‐H2AX foci dose response in PBL exposed to γ‐irradiation: An inter‐ and intra‐laboratory comparison and its relevance for radiation triage

荧光 分子生物学 化学 生物 物理 光学
作者
Venkateswarlu Raavi,Selvan G. Tamizh,Manivannan Bhavani,Arun Kumar,Amit Alok,Kanagaraj Karthik,Namita Kalra,J. Vijayalakshmi,Solomon F.D. Paul,N. K. Chaudhury,Perumal Venkatachalam
出处
期刊:Cytometry Part A [Wiley]
卷期号:87 (12): 1138-1146 被引量:22
标识
DOI:10.1002/cyto.a.22729
摘要

Abstract Measurement of γ‐H2AX protein changes in the peripheral blood lymphocytes (PBL) of individuals exposed to ionizing radiation is a simple, sensitive, and rapid assay for radiation triage and early marker of dose estimation. The qualitative and quantitative measurements of the protein changes were examined using flow cytometry and microscopy. Whole blood and isolated lymphocytes were exposed in vitro between 0.1 and 5 Gy doses of 60 Co γ‐radiation at a dose rate of 1 Gy/min. Radiation induced γ‐H2AX foci frequency ( n = 3) and relative fluorescence intensity ( n = 7) in PBL was measured at 0.5 and 2 hrs postexposure. The observed dose response for γ‐H2AX foci frequency at both time points, for whole blood and isolated lymphocytes did not show any significant ( P > 0.05) differences. However, when compared with γ‐H2AX foci frequency scored manually (microscopy), the semiautomated analysis (captured images) showed a better correlation ( r 2 = 0.918) than that obtained with automated (Metafer) scoring ( r 2 = 0.690). It is noteworthy to mention that, the γ‐H2AX foci frequency quantified using microscopy showed a dose dependent increase up to 2 Gy and the relative fluorescence intensity (RFI) measured with flow cytometry revealed an increase up to 5 Gy in the PBL exposed in vitro. Moreover, a better correlation was observed between the γ‐H2AX foci frequency obtained by manual scoring and RFI ( r 2 = 0.910). Kinetic studies showed that the γ‐H2AX foci remain more or less unchanged up to 4 hrs and reduces gradually over 48 hrs of postexposure at 37°C. Further, inter and intra‐laboratory comparisons showed consistency in the scoring of γ‐H2AX foci frequency by manual and semiautomated scoring. The overall results suggest that measurement of γ‐H2AX (microscopy and flow cytometry) should be employed within 4 to 6 hrs for a reliable dosimetry either by sharing the work load between the laboratories or investing more manpower; however, triage can be possible even up to 48 hrs of postirradiation. © 2015 International Society for Advancement of Cytometry
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