Rajagopalan Pavithra, Nanjappa Vishalakshi, Raja Remya, Jain Ankit P, Mangalaparthi Kiran K, Sathe Gajanan J, Babu Niraj, Patel Krishna, Cavusoglu Nükhet, Soeur Jeremie, Pandey Akhilesh, Roy Nita, Breton Lionel, Chatterjee Aditi, Misra Namita, Gowda Harsha
1 Institute of Bioinformatics , International Tech Park, Bangalore, India .
2 School of Biotechnology, KIIT University , Bhubaneswar, India .
OMICS. 2016 Nov;20(11):615-626. doi: 10.1089/omi.2016.0123.
Cigarette smoking has been associated with multiple negative effects on human skin. Long-term physiological effects of cigarette smoke are through chronic and not acute exposure. Molecular alterations due to chronic exposure to cigarette smoke remain unclear. Primary human skin keratinocytes chronically exposed to cigarette smoke condensate (CSC) showed a decreased wound-healing capacity with an increased expression of NRF2 and MMP9. Using quantitative proteomics, we identified 4728 proteins, of which 105 proteins were overexpressed (≥2-fold) and 41 proteins were downregulated (≤2-fold) in primary skin keratinocytes chronically exposed to CSC. We observed an alteration in the expression of several proteins involved in maintenance of epithelial barrier integrity, including keratin 80 (5.3 fold, p value 2.5 × 10), cystatin A (3.6-fold, p value 3.2 × 10), and periplakin (2.4-fold, p value 1.2 × 10). Increased expression of proteins associated with skin hydration, including caspase 14 (2.2-fold, p value 4.7 × 10) and filaggrin (3.6-fold, p value 5.4 × 10), was also observed. In addition, we report differential expression of several proteins, including adipogenesis regulatory factor (2.5-fold, p value 1.3 × 10) and histone H1.0 (2.5-fold, p value 6.3 × 10) that have not been reported earlier. Bioinformatics analyses demonstrated that proteins differentially expressed in response to CSC are largely related to oxidative stress, maintenance of skin integrity, and anti-inflammatory responses. Importantly, treatment with vitamin E, a widely used antioxidant, could partially rescue adverse effects of CSC exposure in primary skin keratinocytes. The utility of antioxidant-based new dermatological formulations in delaying or preventing skin aging and oxidative damages caused by chronic cigarette smoke exposure warrants further clinical investigations and multi-omics research.
吸烟已被证明会对人体皮肤产生多种负面影响。香烟烟雾的长期生理影响是通过慢性而非急性暴露产生的。长期接触香烟烟雾所导致的分子变化仍不清楚。长期暴露于香烟烟雾冷凝物(CSC)的原代人皮肤角质形成细胞显示出伤口愈合能力下降,同时NRF2和MMP9的表达增加。通过定量蛋白质组学,我们鉴定出4728种蛋白质,其中105种蛋白质在长期暴露于CSC的原代皮肤角质形成细胞中过表达(≥2倍),41种蛋白质下调(≤2倍)。我们观察到几种参与维持上皮屏障完整性的蛋白质表达发生改变,包括角蛋白80(5.3倍,p值2.5×10)、胱抑素A(3.6倍,p值3.2×10)和外周蛋白(2.4倍,p值1.2×10)。还观察到与皮肤水合作用相关的蛋白质表达增加,包括半胱天冬酶14(2.2倍,p值4.7×10)和丝聚合蛋白(3.6倍,p值5.4×10)。此外,我们报告了几种蛋白质的差异表达,包括脂肪生成调节因子(2.5倍,p值1.3×10)和组蛋白H1.0(2.5倍,p值6.3×10),这些蛋白质此前尚未见报道。生物信息学分析表明,响应CSC而差异表达的蛋白质在很大程度上与氧化应激、皮肤完整性维持和抗炎反应有关。重要的是,广泛使用的抗氧化剂维生素E处理可以部分挽救CSC暴露对原代皮肤角质形成细胞产生的不利影响。基于抗氧化剂的新型皮肤病学制剂在延缓或预防慢性香烟烟雾暴露引起的皮肤衰老和氧化损伤方面的效用值得进一步的临床研究和多组学研究。