590 nm LED Irradiation Improved Erythema through Inhibiting Angiogenesis of Human Microvascular Endothelial Cells and Ameliorated Pigmentation in Melasma

黄褐斑 PI3K/AKT/mTOR通路 血管生成 蛋白激酶B 血管内皮生长因子 癌症研究 内皮干细胞 细胞生物学 红斑 医学 生长因子 化学 磷酸化 内分泌学 信号转导 生物 免疫学 体外 皮肤病科 内科学 生物化学 血管内皮生长因子受体 受体
作者
Xiaoxi Dai,Shanglin Jin,Yijie Xuan,Yiwen Yang,Xiaoli Lu,Chen Wang,Li Chen,Leihong Xiang,Chengfeng Zhang
出处
期刊:Cells [Multidisciplinary Digital Publishing Institute]
卷期号:11 (24): 3949-3949 被引量:21
标识
DOI:10.3390/cells11243949
摘要

Melasma is a common refractory acquired pigmentary skin disease that mainly affects middle-aged women. The pathogenesis of melasma is still uncertain, while abnormal vascular endothelial cells may play a role. We previously demonstrated the yellow light of light-emitting diodes (LED) could inhibit melanogenesis through the photobiomodulation (PBM) of melanocytes and keratinocytes. In the current study, we investigated the effect of 590 nm LED on the function of human microvascular endothelial cells (HMEC-1). We revealed 0–40 J/cm2 590 nm LED had no toxic effect on HMEC-1 in vitro. 590 nm LED irradiation significantly reduced cell migration, tube formation, as well as the expression of vascular endothelial growth factor (VEGF) and stem cell factor (SCF), a pro-melanogenic factor. Moreover, we illustrated that 590 nm LED inhibited the phosphorylation of the AKT/PI3K/mTOR signaling pathway, and the inhibitory effect on HMEC-1 could be partially reversed by insulin-like growth factor 1 (IGF-1), an AKT/PI3K/mTOR pathway agonist. Besides, we conducted a pilot clinical study and observed a marked improvement on facial erythema and pigmentation in melasma patients after amber LED phototherapy. Taken together, 590 nm LED inhibited HMEC-1 migration, tube formation and the secretion of VEGF and SCF, predominantly through the inhibition of the AKT/PI3K/mTOR pathway, which may serve as a novel therapeutic option for melasma.
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