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]
日期:2022-12-07
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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