Pageon Hervé, Zucchi Hélène, Ricois Sylvie, Bastien Philippe, Asselineau Daniel
Department and Institution, L'Oréal Research & Innovation, Avenue Eugène Schueller, Aulnay-sous-Bois 93600, France.
J Aging Res. 2021 Oct 26;2021:6647773. doi: 10.1155/2021/6647773. eCollection 2021.
Skin aging is the result of superimposed intrinsic (individual) and extrinsic (e.g., UV exposure or nutrition) aging. Previous works have reported a relationship between UV irradiation and glycation in the aging process, leading, for example, to modified radical species production and the appearance of AGEs (advanced glycosylation end products) in increasing quantities, particularly glycoxidation products like pentosidine. In addition, the colocalization of AGEs and elastosis has also been observed. We first investigated the combination of the glycation reaction and UVA effects on a reconstructed skin model to explain their cumulative biological effect. We found that UVA exposure combined with glycation had the ability to intensify the response for specific markers: for example, MMP1 or MMP3 mRNA, proteases involved in extracellular matrix degradation, or proinflammatory cytokine, IL1, protein expression. Moreover, the association of glycation and UVA irradiation is believed to promote an environment that favors the onset of an elastotic-like phenomenon: mRNA coding for elastin, elastase, and tropoelastin expression is increased. Secondly, because the damaging effects of UV radiation might be more detrimental in aged skin than in young skin due to increased accumulation of pentosidine and the exacerbation of alterations related to chronological aging, we studied the biological effect of soluble pentosidine in fibroblasts grown in monolayers. We found that pentosidine induced upregulation of CXCL2, IL8, and MMP12 mRNA expression (inflammatory and elastotic markers, respectively). Tropoelastin protein expression (elastin precursor) was also increased. In conclusion, fibroblasts in monolayers cultured with soluble pentosidine and tridimensional skin constructs exposed to the combination of AGEs and UVA promote an inflammatory state and an alteration of the dermal compartment in relation to an elastosis-like environment.
皮肤老化是内在(个体)老化和外在(如紫外线照射或营养)老化叠加的结果。先前的研究报告了紫外线照射与老化过程中糖基化之间的关系,例如,导致自由基种类产生的改变以及晚期糖基化终产物(AGEs)数量的增加,特别是像戊糖苷这样的糖氧化产物。此外,还观察到了AGEs与弹性组织变性的共定位。我们首先研究了糖基化反应与UVA对重建皮肤模型的影响的组合,以解释它们的累积生物学效应。我们发现,UVA照射与糖基化相结合能够增强对特定标志物的反应:例如,MMP1或MMP3 mRNA,参与细胞外基质降解的蛋白酶,或促炎细胞因子IL1的蛋白表达。此外,糖基化与UVA照射的关联被认为会促进一种有利于类弹性组织变性现象发生的环境:编码弹性蛋白、弹性蛋白酶和原弹性蛋白表达的mRNA增加。其次,由于紫外线辐射的损伤作用在老年皮肤中可能比在年轻皮肤中更具危害性,这是由于戊糖苷的积累增加以及与自然老化相关的改变加剧,我们研究了可溶性戊糖苷对单层培养的成纤维细胞的生物学效应。我们发现戊糖苷诱导CXCL2、IL8和MMP12 mRNA表达上调(分别为炎症和弹性组织变性标志物)。原弹性蛋白蛋白表达(弹性蛋白前体)也增加。总之,用可溶性戊糖苷培养的单层成纤维细胞和暴露于AGEs与UVA组合的三维皮肤构建体促进了炎症状态以及与类弹性组织变性环境相关的真皮层改变。