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黄芩素通过激活 NF-E2 相关因子 2(Nrf2)信号通路保护人白癜风黑素细胞免受氧化应激。

Baicalein protects human vitiligo melanocytes from oxidative stress through activation of NF-E2-related factor2 (Nrf2) signaling pathway.

机构信息

Department of Dermatology, Xijing Hospital, Fourth Military Medical University, No. 127 Changlexi Road, Xi'an 710032, Shaanxi, China.

Department of Dermatology, Xijing Hospital, Fourth Military Medical University, No. 127 Changlexi Road, Xi'an 710032, Shaanxi, China.

出版信息

Free Radic Biol Med. 2018 Dec;129:492-503. doi: 10.1016/j.freeradbiomed.2018.10.421. Epub 2018 Oct 18.

Abstract

Vitiligo is a complex disorder characterized by patchy loss of skin pigmentation due to abnormal melanocyte function. Overwhelming evidences have suggested that oxidative stress plays a major role in the loss of melanocytes thereby mediating the onset and progression of vitiligo. The nuclear factor erythroid 2-like factor 2 (Nrf2) is a master regulator of cellular redox homeostasis and the activation of Nrf2 signaling pathway is impaired in the vitiligo melanocytes. Baicalein, as flavonoid extracted from the Scutellaria baicalensis, has been proved to possess the ability to activate Nrf2 signaling pathway in other cell types and mouse model. Our previous data found that baicalein exerts a cytoprotective role in HO-induced apoptosis in human melanocytes cell line (PIG1). Based on these founding, we hypothesized that baicalein activates Nrf2 signaling pathway, alleviates HO-induced mitochondrial dysfunction and cellular damage, thereby protecting human vitiligo melanocytes from oxidative stress. In the present study, we found that baicalein effectively inhibited HO-induced cytotoxicity and apoptosis in human vitiligo melanocytes (PIG3V). Further results demonstrated that baicalein promoted Nrf2 nucleus translocation as well as up-regulated the expression of Nrf2 and its target gene, heme oxygenase-1 (HO-1). Moreover, the protective effects of baicalein against HO-induced cellular damage and apoptosis as well as mitochondrial dysfunction were abolished by Nrf2 knockdown. Additionally, we observed that Nrf2 knockdown suppressed proliferation and increased the sensitivity of PIG3V cells to HO treatment. Finally, we explored the mechanism of baicalein associated with Nrf2 activation and found that the phosphorylation of Nrf2 as well as ERK1/2and PI3K/AKT signaling were not involved in the baicalein-induced activation of Nrf2. Taken together, these data clearly suggest that baicalein enhances cellular antioxidant defense capacity of human vitiligo melanocytes through the activation of the Nrf2 signaling pathway, providing beneficial evidence for the application of baicalein in the vitiligo treatment.

摘要

白癜风是一种复杂的疾病,其特征是由于黑素细胞功能异常导致皮肤色素沉着不均匀丧失。大量证据表明,氧化应激在黑素细胞丧失中起主要作用,从而介导白癜风的发生和进展。核因子红细胞 2 样因子 2(Nrf2)是细胞氧化还原稳态的主要调节剂,而白癜风黑素细胞中的 Nrf2 信号通路的激活受到损害。黄芩素是从黄芩中提取的一种黄酮类化合物,已被证明能够在其他细胞类型和小鼠模型中激活 Nrf2 信号通路。我们之前的数据发现,黄芩素在 HO 诱导的人黑素细胞系(PIG1)凋亡中发挥细胞保护作用。基于这些发现,我们假设黄芩素激活 Nrf2 信号通路,减轻 HO 诱导的线粒体功能障碍和细胞损伤,从而保护人白癜风黑素细胞免受氧化应激。在本研究中,我们发现黄芩素能有效抑制 HO 诱导的人白癜风黑素细胞(PIG3V)的细胞毒性和凋亡。进一步的结果表明,黄芩素促进了 Nrf2 的核易位以及 Nrf2 及其靶基因血红素加氧酶-1(HO-1)的表达上调。此外,Nrf2 敲低消除了黄芩素对 HO 诱导的细胞损伤和凋亡以及线粒体功能障碍的保护作用。此外,我们观察到 Nrf2 敲低抑制了 PIG3V 细胞的增殖并增加了其对 HO 处理的敏感性。最后,我们探讨了与 Nrf2 激活相关的黄芩素的作用机制,发现 Nrf2 的磷酸化以及 ERK1/2 和 PI3K/AKT 信号通路不参与黄芩素诱导的 Nrf2 激活。总之,这些数据清楚地表明,黄芩素通过激活 Nrf2 信号通路增强了人白癜风黑素细胞的细胞抗氧化防御能力,为黄芩素在白癜风治疗中的应用提供了有益的证据。

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