Burón María, Palomares Teodoro, Garrido-Pascual Patricia, Herrero de la Parte Borja, García-Alonso Ignacio, Alonso-Varona Ana
Department of Cell Biology and Histology, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), 48940 Leioa, Bizkaia, Spain.
Department of Surgery, Radiology and Physical Medicine, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), 48940 Leioa, Bizkaia, Spain.
Antioxidants (Basel). 2022 Oct 11;11(10):2011. doi: 10.3390/antiox11102011.
Human skin exposure to ultraviolet B (UVB) radiation can result in acute photodamage through oxidative modifications of cellular components and biomolecules involved in the metabolism of dermal cells. Recently, the therapeutic potential of human adipose-derived stem cells (hASCs) has been investigated as a novel strategy for photoprotection due to their pro-angiogenic properties, protective activity against oxidative stress and paracrine effect on dermal cells. To enhance these therapeutic properties, hASCs can be preconditioned by exposing them to sublethal cellular stressors. In this study, we first analyzed response capacity against UVB-induced oxidative stress in HO-preconditioned hASCs (called HC016 cells); and second, we evaluated the photoprotective effect of HC016-conditioned medium (CM) in an in vitro UVB irradiation model in cultured human foreskin fibroblasts (hFFs). The results demonstrated that HC016 cells have a greater capacity to respond efficiently to UVB-induced oxidative stress, evidenced by higher Nrf2 antioxidant system activity and enhanced viability and migration capacity. Further, HC016-CM treatment increased viability, migratory capacity and collagen type I synthesis in hFFs exposed to UVB radiation, as well as reducing their cytotoxicity, apoptosis, senescence and IL-6 secretion. Collectively, these findings support the view that HC016 cells could protect against UVB-induced photodamage via paracrine mechanisms.
人体皮肤暴露于中波紫外线(UVB)辐射下,可通过对参与真皮细胞代谢的细胞成分和生物分子进行氧化修饰,导致急性光损伤。最近,由于人脂肪来源干细胞(hASCs)具有促血管生成特性、抗氧化应激保护活性以及对真皮细胞的旁分泌作用,其治疗潜力已被作为一种光保护新策略进行研究。为增强这些治疗特性,可通过将hASCs暴露于亚致死性细胞应激源对其进行预处理。在本研究中,我们首先分析了经血红素氧合酶预处理的hASCs(称为HC016细胞)对UVB诱导的氧化应激的反应能力;其次,我们在体外培养的人包皮成纤维细胞(hFFs)的UVB照射模型中评估了HC016条件培养基(CM)的光保护作用。结果表明,HC016细胞对UVB诱导的氧化应激具有更强的有效反应能力,这表现为更高的Nrf2抗氧化系统活性以及增强的活力和迁移能力。此外,HC016-CM处理可提高暴露于UVB辐射的hFFs的活力、迁移能力和I型胶原蛋白合成,同时降低其细胞毒性、细胞凋亡、衰老和IL-6分泌。总的来说,这些发现支持了HC016细胞可通过旁分泌机制预防UVB诱导的光损伤这一观点。