Hu Meijun, Hu Liang, Yang Tao, Zhou Bowen, Feng Xuanhe, Fan Zhipeng, Shan Zhaochen
Laboratory of Molecular Signaling and Stem Cells Therapy, Beijing Key Laboratory of Tooth Regeneration and Function Reconstruction, School of Stomatology, Capital Medical University, Beijing 100050, China.
Outpatient Department of Oral and Maxillofacial Surgery, School of Stomatology, Capital Medical University, Beijing 100050, China.
Antioxidants (Basel). 2024 Jul 26;13(8):904. doi: 10.3390/antiox13080904.
Radiation-induced salivary gland injury (RISGI) is a common complication of radiotherapy in patients with head and neck cancer. Intragland expression of the Sonic Hedgehog (Shh) gene may partially rescue irradiation (IR)-induced hyposalivation by preserving salivary stem/progenitor cells and parasympathetic innervation, maintaining resident macrophages, and maintaining microvascular density. Previous studies have revealed that Ad-Rat Shh transduction through the salivary glands of miniature pigs can ameliorate oxidative stress-induced microvascular dysfunction after radiotherapy. Changes in the parotid salivary flow rate were analyzed, and the parotid tissue was collected at 5 and 20 weeks after IR. Changes in the Hedgehog pathway and vascular function-related markers (vascular endothelial growth factor (VEGF) and CD31) and oxidative stress-related markers were detected via immunohistochemistry, immunofluorescence, and Western blotting. A stable Shh-overexpressing cell line was generated from human umbilical vein endothelial cells (HUVECs) and exposed to 10 Gy X-ray irradiation, after which endothelial cell proliferation, senescence, apoptosis, and vascular function were evaluated. We found that intragland expression of the Shh gene efficiently alleviated IR-induced parotid gland injury in a miniature pig model. Our results indicate that the antioxidative stress and microvascular-protective effects of the Hh pathway are regulated by nuclear factor-erythroid 2-related factor 2 (Nrf2).
放射性唾液腺损伤(RISGI)是头颈部癌患者放疗常见的并发症。音猬因子(Shh)基因在腺体内的表达可通过保留唾液腺干/祖细胞和副交感神经支配、维持驻留巨噬细胞以及维持微血管密度,部分缓解辐射(IR)诱导的唾液分泌减少。先前的研究表明,通过小型猪的唾液腺进行腺相关病毒-大鼠Shh转导,可改善放疗后氧化应激诱导的微血管功能障碍。分析腮腺唾液流速的变化,并在IR后5周和20周收集腮腺组织。通过免疫组织化学、免疫荧光和蛋白质印迹法检测Hedgehog信号通路及血管功能相关标志物(血管内皮生长因子(VEGF)和CD31)以及氧化应激相关标志物的变化。从人脐静脉内皮细胞(HUVECs)构建稳定的Shh过表达细胞系,并使其暴露于10 Gy X射线照射下,之后评估内皮细胞的增殖、衰老、凋亡及血管功能。我们发现,在小型猪模型中,Shh基因在腺体内的表达有效减轻了IR诱导的腮腺损伤。我们的结果表明,Hh信号通路的抗氧化应激和微血管保护作用由核因子红细胞2相关因子2(Nrf2)调控。