2022
DOI: 10.1016/j.jphotobiol.2022.112388
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Red and near infrared light-stimulated angiogenesis mediated via Ca2+ influx, VEGF production and NO synthesis in endothelial cells in macrophage or malignant environments

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Cited by 16 publications
(17 citation statements)
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“…To date, the most discussed photoacceptor is cytochrome c oxidase (CCO) (6,13). CCO absorbs red/NIR light within wavelengths ranging between 600 and 1000 nm, resulting in the activation of metabolic process as well as migration and proliferation of various cell types: neurons (650–660/808 nm at 3–90 J cm −2 (3,4,14), fibroblasts (660 nm at 5 J cm −2 (15), 660 nm at 3–8 J cm −2 (16), 809 nm at 1.96–7.84 J cm −2 (17)), endothelial cells (635 nm at 24 J cm −2 (18), 650 nm at 30 J cm −2 (19), 665 and 675 nm at 10 J cm −2 (20), 808 nm at 60 J cm −2 (21)), stem cells (660 nm (22,23) and 808 nm at 3 J cm −2 (24)), keratinocytes (780 nm at 0.45–0.95 J cm −2 (25)), lymphocytes (660 nm at 0–5.0 J cm −2 (26), 820 nm at 1.2–8.4 J cm −2 (27)), macrophages (650/808 nm at 3–90 J cm −2 (28)), cancer cells (650/808 nm at 3–90 J cm −2 (3,4), 830 nm at 2 J cm −2 (29)), rat pre‐odontoblast cells (980 nm at 0.65–6.5 J cm −2 (30)), rat satellite cells (632.8 nm at 0.18 J cm −2 (31)), myoblast cells (808 nm at 10–70 J cm −2 (32)) and other cells (33–35).…”
Section: Introductionmentioning
confidence: 99%
“…To date, the most discussed photoacceptor is cytochrome c oxidase (CCO) (6,13). CCO absorbs red/NIR light within wavelengths ranging between 600 and 1000 nm, resulting in the activation of metabolic process as well as migration and proliferation of various cell types: neurons (650–660/808 nm at 3–90 J cm −2 (3,4,14), fibroblasts (660 nm at 5 J cm −2 (15), 660 nm at 3–8 J cm −2 (16), 809 nm at 1.96–7.84 J cm −2 (17)), endothelial cells (635 nm at 24 J cm −2 (18), 650 nm at 30 J cm −2 (19), 665 and 675 nm at 10 J cm −2 (20), 808 nm at 60 J cm −2 (21)), stem cells (660 nm (22,23) and 808 nm at 3 J cm −2 (24)), keratinocytes (780 nm at 0.45–0.95 J cm −2 (25)), lymphocytes (660 nm at 0–5.0 J cm −2 (26), 820 nm at 1.2–8.4 J cm −2 (27)), macrophages (650/808 nm at 3–90 J cm −2 (28)), cancer cells (650/808 nm at 3–90 J cm −2 (3,4), 830 nm at 2 J cm −2 (29)), rat pre‐odontoblast cells (980 nm at 0.65–6.5 J cm −2 (30)), rat satellite cells (632.8 nm at 0.18 J cm −2 (31)), myoblast cells (808 nm at 10–70 J cm −2 (32)) and other cells (33–35).…”
Section: Introductionmentioning
confidence: 99%
“…Studies have shown that appropriate local photothermal effects can accelerate microcirculatory blood flow, stimulate angiogenesis and thus promote wound healing. 68 As illustrated in Fig. 4a, the temperature of the ZPTA-G/HMA group rose to 48.83 ± 0.84 °C within 30 min under NIR (1.0 W cm −2 ) irradiation, while that of the G/HMA group and PBS group only rose to 32.40 ± 0.98 °C and 28.54 ± 0.55 °C, respectively.…”
Section: Resultsmentioning
confidence: 81%
“…Previous studies demonstrated the modulation of M1/M2 polarization of microglia under NIR treatment. [16,[45][46][47] Stepanov et al observed that red/NIR light significantly increased the percentage of M2 macrophages secreting VEGF and promoting endothelial cell proliferation. [45] Leden et al showed that low-energy density 808-nm light altered M1/M2 polarization and reduced the release of pro-inflammatory factors.…”
Section: Discussionmentioning
confidence: 99%