State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210023, China.
State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing 210023, China; Quanzhou Institute for Environment Protection Industry, Nanjing University, Quanzhou 362000, China.
Sci Total Environ. 2023 Sep 10;890:164374. doi: 10.1016/j.scitotenv.2023.164374. Epub 2023 May 24.
The use of face paint cosmetics can cause skin diseases in opera performers due to the presence of heavy metals and other toxic ingredients in the cosmetics. However, the underlying molecular mechanism for these diseases remains unknown. Here we examined the transcriptome gene profile of human skin keratinocytes exposed to artificial sweat extracts of face paints, and identified the key regulatory pathways and genes, using RNA sequencing technique. Bioinformatics analyses suggested that the face paint exposure induced the differentially expression of 1531 genes and enriched inflammation-relevant TNF and IL-17 signaling pathways after just 4 h of exposure. Inflammation-relevant genes CREB3L3, FOS, FOSB, JUN, TNF, and NFKBIA were identified as the potential regulatory genes, and SOCS3 capable to prevent inflammation-induced carcinogenesis as the hub-bottleneck gene. Long-term exposure (24 h) could exacerbate inflammation, accompanied by interference in cellular metabolism pathways, and the potential regulatory genes (ATP1A1, ATP1B1, ATP1B2, FXYD2, IL6, and TNF) and hub-bottleneck genes (JUNB and TNFAIP3) were all related to inflammation induction and other adverse responses. We proposed that the exposure to face paint might cause the inflammatory factors TNF and IL-17, which are encoded by the genes TNF and IL17, to bind to receptors and activate TNF and IL-17 signaling pathways, leading to the expression of cell proliferation factors (CREB and AP-1) and proinflammatory mediators including transcription factors (FOS, JUN, and JUNB), inflammatory factors (TNF-α and IL6), and intracellular signaling factors (TNFAIP3). This finally resulted in cell inflammation, apoptosis, and other skin diseases. TNF was identified as the key regulator and connector in all the enriched signaling pathways. Our study provides the first insights into the cytotoxicity mechanism of face paints to skin cells and highlights the need for stricter regulations in face paint safety.
使用面部彩绘化妆品会导致歌剧演员出现皮肤病,因为化妆品中含有重金属和其他有毒成分。然而,这些疾病的潜在分子机制尚不清楚。在这里,我们使用 RNA 测序技术检查了暴露于人工汗液提取的面部彩绘化妆品的人皮肤角质形成细胞的转录组基因谱,并鉴定了关键的调控途径和基因。生物信息学分析表明,暴露于面部彩绘仅 4 小时后,暴露就会诱导 1531 个基因的差异表达,并富集与炎症相关的 TNF 和 IL-17 信号通路。鉴定出与炎症相关的基因 CREB3L3、FOS、FOSB、JUN、TNF 和 NFKBIA 为潜在的调节基因,而 SOCS3 作为潜在的枢纽-瓶颈基因能够防止炎症诱导的癌变。长期暴露(24 小时)会加剧炎症,同时干扰细胞代谢途径,潜在的调节基因(ATP1A1、ATP1B1、ATP1B2、FXYD2、IL6 和 TNF)和枢纽-瓶颈基因(JUNB 和 TNFAIP3)都与炎症诱导和其他不良反应有关。我们提出,暴露于面部彩绘可能会导致炎症因子 TNF 和 IL-17,它们分别由 TNF 和 IL17 基因编码,与受体结合并激活 TNF 和 IL-17 信号通路,导致细胞增殖因子(CREB 和 AP-1)和促炎介质的表达,包括转录因子(FOS、JUN 和 JUNB)、炎症因子(TNF-α和 IL6)和细胞内信号因子(TNFAIP3)。这最终导致细胞炎症、细胞凋亡和其他皮肤病。TNF 被鉴定为所有富集信号通路中的关键调节剂和连接器。我们的研究首次揭示了面部彩绘对皮肤细胞的细胞毒性机制,并强调需要对面部彩绘安全性进行更严格的监管。