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. Author manuscript; available in PMC: 2016 Dec 1.
Published in final edited form as: J Photochem Photobiol B. 2015 Sep 14;153:153–163. doi: 10.1016/j.jphotobiol.2015.09.012

Fig. 2.

Fig. 2

Proliferative responses (incorporation of 3H-thymidine) of non-treated and photoinactivated B6D2F1/J spleen cells to Concanavalin A (ConA; 2.5 µg ml−1), phytohemagglutinin (PHA; 15 µg ml−1), lipopolysaccharide (LPS; 5 µg ml−1), and interleukin-2 (IL-2; 25 U ml−1). Data represent means ± standard errors (SE) of 9 determinations derived from 3 independent experiments. Background activity (incorporation of 3H-thymidine by non-stimulated cells) was 3500 to 4500 cpm. N: Cells exposed to neither dye nor light. L: Cells exposed to light (189 kJ m−2) but no dye. D: Cells exposed to dye (15 µg ml−1) but no light. Suppressions of proliferative responses were statistically significant (p<0.05; 2-tailed Student's t-test) for cells exposed to MC540 and light fluences of ≥63 kJ m−2 (panels a and c) and for cells exposed to MC540 and light fluences of ≥32 kJ m−2) (panels b and d).