Live Dynamics of 53BP1 Foci Following Simultaneous Induction of Clustered and Dispersed DNA Damage in U2OS Cells

• Published in: International journal of molecular sciences Vol. 19; no. 2; p. 519
• Main Authors: Sollazzo, Alice, Brzozowska, Beata, Cheng, Lei, Lundholm, Lovisa, Scherthan, Harry, Wojcik, Andrzej
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 08.02.2018; MDPI
• Subjects: 53BP1 foci; Alpha particles; Alpha rays; Beams (radiation); Chromatin; clustered DSB; Deoxyribonucleic acid; DNA; DNA damage; Double-strand break repair; Fluorescence; live cell imaging; Molecular Bioscience; molekylär biovetenskap; Particle beams; Radiation effects; X-rays; alpha particles; live cell imaging; 53BP1 foci; clustered DSB; X-rays
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms19020519

Cells react differently to clustered and dispersed DNA double strand breaks (DSB). Little is known about the initial reaction to simultaneous induction of DSBs with different complexities. Here, we used live cell microscopy to analyse the behaviour of 53BP1-GFP (green fluorescence protein) foci formation at DSBs induced in U2OS cells by alpha particles, X-rays or mixed beams over a 75 min period post irradiation. X-ray-induced foci rapidly increased and declined over the observation interval. After an initial increase, mixed beam-induced foci remained at a constant level over the observation interval, similarly as alpha-induced foci. The average areas of radiation-induced foci were similar for mixed beams and X-rays, being significantly smaller than those induced by alpha particles. Pixel intensities were highest for mixed beam-induced foci and showed the lowest level of variability over time as compared to foci induced by alphas and X-rays alone. Finally, mixed beam-exposed foci showed the lowest level of mobility as compared to alpha and X-ray exposure. The results suggest paralysation of chromatin around foci containing clustered DNA damage.