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Fig. S1. Exemplary histoplot (1/9; see Fig. 6) of annexin V fluorescence after vital staining in PI-negative cells. For each sample 10 000 cells were counted and the mean fluorescence intensity of each sample was calculated from the respective histogram. X-axis: intensity of green fluorescence (annexin V), emission filter 530nm±15nm. Y-axis: number of cells with corresponding fluorescence intensity (colour code: black – control; light green – 411 nm, 0.6 W/m2; dark green – 411 nm, 1.5 W/m2; red – 411 nm, 4.5 W/m2; orange – 470 nm, 4.5 W/m2). Note the shift in FL1-H with increasing irradiance at 411nm light irradiation (red curve).

Fig. S2. Exemplary histoplot (1/9; see Fig. 7) of PI-stained cells (subG1 DNA content analysis). For each sample 10 000 cells were counted and the mean fluorescence intensity of each sample was calculated from the respective histogram. X-axis: intensity of red fluorescence (PI), emission filter 585 nm ± 21 nm. Y-axis: number of cells with corresponding fluorescence intensity (colour code: black – control; light green – 411 nm, 0.6 W/m2; dark green – 411 nm, 1.5 W/m2; red – 411 nm, 4.5 W/m2; orange – 470 nm, 4.5 W/m2). M1 – the range of cells with fragmented nuclei (sub G1-DNA content). Note the shift in FL2-H after irradiation of 411 nm light at an irradiance of 4.5 W/m2 (red curve).

Fig. S3. Exemplary histoplot (1/6; see Fig. 4) of mitosox-stained cells (mitochondrial superoxide radical production). For each sample 10 000 cells were counted and the median fluorescence intensity of each sample was calculated from the respective histogram. X-axis: intensity of red fluorescence (mitosox), emission filter 585 nm ± 21 nm. Y-axis: number of cells with corresponding fluorescence intensity (colour code: black – control; light green – 411 nm, 0.6 W/m2; dark green – 411 nm, 1.5 W/m2; red – 411 nm, 4.5 W/m2; orange – 470 nm, 4.5 W/m2). Note the shift in FL2-H after irradiation of 411 nm light at an irradiance of 4.5 W/m2 (red curve).

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