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. 2017 Jun 5;7:2797. doi: 10.1038/s41598-017-02802-0

Figure 7.

Figure 7

Impact of blue (450 nm) and NIR (850 nm) light treatment on the metabolic activity of human dermal fibroblasts when exposed to dermal tissue oxygen levels (approx. 2%). (A) Fluorescence counts (Alamar Blue) measured in reticular and papillary fibroblasts (facelift, female, 64 yo) in low (2%) and high (20%) oxygen levels. No strong change in Alamar fluorescence count is apparent. (B) Relative cell counts of human dermal fibroblasts (reticular and papillary) after light treatment in hypoxic conditions (2% oxygen). Cells were grown in 35-mm individual dishes and treated with light once a day for three consecutive days. Cell counting was performed 24 h after last treatment. Material originating from two different donors was included in the experiment (N = 2, reticular and papillary, 3 repeats, 12 counts per bar). (C) Relative metabolic activity of human papillary fibroblasts in response to 30 J.cm−2 at 450 nm in low and high environmental oxygen levels (N = 2, papillary and 3 replicates). (D) Relative metabolic activity of human reticular fibroblasts in response to 20 J.cm−2 at 850 nm in low and high environmental oxygen levels (N = 2, reticular and 3 replicates). Irradiance levels were 50 mW.cm−2 (450 nm) and 80 mW.cm−2 (850 nm).