Guerrero-Navarro Lena, Martic Ines, Ploner Christian, Jansen-Dürr Pidder, Cavinato Maria
Institute for Biomedical Aging Research, Universität Innsbruck, 6020 Innsbruck, Austria.
Center for Molecular Biosciences Innsbruck (CMBI), 6020 Innsbruck, Austria.
Biomedicines. 2024 Mar 6;12(3):592. doi: 10.3390/biomedicines12030592.
Cellular senescence, a state of irreversible growth arrest, is implicated in various age-related pathologies, including skin aging. In this study, we investigated the role of CLCA2, a calcium-activated chloride channel accessory protein, in cellular senescence and its implications for skin aging. Utilizing UVB and Nutlin3a-induced senescence models, we observed the upregulation of CLCA2 at both transcriptomic and proteomic levels, suggesting its involvement in senescence pathways. Further analysis revealed that the depletion of CLCA2 led to accelerated senescence onset, characterized by classic senescence markers and a unique secretome profile. In 3D skin equivalent models, SEs constructed with CLCA2 knockdown fibroblasts exhibited features reminiscent of aged skin, underscoring the importance of CLCA2 in maintaining skin homeostasis. Our findings highlight CLCA2 as a novel regulator of cellular senescence and its potential implications for skin aging mechanisms.
细胞衰老,一种不可逆的生长停滞状态,与包括皮肤衰老在内的各种与年龄相关的病理状况有关。在本研究中,我们研究了钙激活氯离子通道辅助蛋白CLCA2在细胞衰老中的作用及其对皮肤衰老的影响。利用紫外线B(UVB)和Nutlin3a诱导的衰老模型,我们在转录组和蛋白质组水平上均观察到CLCA2的上调,表明其参与衰老途径。进一步分析表明,CLCA2的缺失导致衰老起始加速,其特征为经典的衰老标志物和独特的分泌组谱。在三维皮肤等效模型中,用CLCA2敲低的成纤维细胞构建的皮肤等效物表现出类似于老化皮肤的特征,突出了CLCA2在维持皮肤稳态中的重要性。我们的研究结果突出了CLCA2作为细胞衰老的一种新型调节因子及其对皮肤衰老机制的潜在影响。