Giroud Joëlle, Delvaux Pauline, Carlier Laura, De Schutter Clémentine, Martin Nathalie, Rouget Raphaël, Bolouki Ayeh, De Glas Valérie, Bouriez Inès, Bourdoux Florent, Burteau Sophie, Théry Julien, Decanter Gauthier, Penel Nicolas, de Launoit Yvan, Ledoux Benjamin, Abbadie Corinne, Poumay Yves, Pluquet Olivier, Debacq-Chainiaux Florence
Laboratory of Biochemistry and Cell Biology (URBC), Namur Research Institute for Life Sciences (NARILIS), University of Namur, Namur, Belgium.
University of Lille, CNRS, Inserm, Pasteur Institute of Lille, UMR9020-U1277-CANTHER-Cancer Heterogeneity Plasticity and Resistance to Therapies, Lille, France.
Aging Cell. 2025 Jun;24(6):e70024. doi: 10.1111/acel.70024. Epub 2025 Apr 16.
Skin aging is influenced by both intrinsic and extrinsic factors, particularly UV radiation, and is characterized by an accumulation of senescent cells. Remarkably, exposure to UV can trigger senescence in different skin cell types, including dermal fibroblasts. However, the molecular mechanisms underlying UV-induced senescence and the impact of the related senescence-associated secretory phenotype (SASP) on the homeostasis of the overlying epidermis remain poorly understood. Here, we identified that both chronological aging and photoaging induce the unfolded protein response (UPR) in human dermal samples. We demonstrated that silencing ATF6α disrupts the establishment of the UVB-induced senescent phenotype by preventing the onset of several senescent biomarkers and alters the composition of the SASP, consequently affecting its impact on the increased proliferation of keratinocytes embedded in reconstructed human epidermis. Moreover, we found that ATF6α partially mediates IL8 expression involved in the hyperproliferation of cultured keratinocytes. Together, our findings highlight the importance of the ATF6α/IL8 axis in regulating the homeostasis of neighboring cells during skin photoaging, thus suggesting ATF6α as a potentially promising target for senotherapeutic interventions.
皮肤衰老受内在和外在因素的影响,尤其是紫外线辐射,其特征是衰老细胞的积累。值得注意的是,紫外线照射可在包括真皮成纤维细胞在内的不同皮肤细胞类型中引发衰老。然而,紫外线诱导衰老的分子机制以及相关衰老相关分泌表型(SASP)对上层表皮稳态的影响仍知之甚少。在这里,我们发现自然衰老和光老化都会在人类真皮样本中诱导未折叠蛋白反应(UPR)。我们证明,沉默ATF6α可通过阻止几种衰老生物标志物的出现来破坏紫外线诱导的衰老表型的建立,并改变SASP的组成,从而影响其对重建人表皮中角质形成细胞增殖增加的影响。此外,我们发现ATF6α部分介导了参与培养角质形成细胞过度增殖的IL8表达。总之,我们的研究结果突出了ATF6α/IL8轴在皮肤光老化过程中调节邻近细胞稳态的重要性,从而表明ATF6α作为衰老治疗干预的潜在有前景的靶点。