State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Department of Oral and Maxillofacial Surgery, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Cell Prolif. 2023 Apr;56(4):e13381. doi: 10.1111/cpr.13381. Epub 2022 Dec 13.
In this study, we investigated the role of tetrahedral framework nucleic acids (tFNAs) in irradiation-induced salivary gland damage in vitro and in vivo. Irradiation-damaged submandibular gland cells (SMGCs) were treated with different concentrations of tFNAs. Cell activity was measured by CCK-8 assay. Cell death was detected by Calcein-AM/PI double staining. Cell apoptosis was assessed by flow cytometry. The expression of apoptosis proteins and inflammatory cytokines were detected by western blot. Body weight, drinking volume, saliva flow rate and lag time was measured 8 weeks after irradiation. Micromorphological changes of submandibular gland were assessed by haematoxylin-eosin and masson staining. Cell proliferation, apoptosis and microvessel density of submandibular gland were evaluated by immunohistochemical staining. tFNAs could promote cell proliferation, inhibit cell apoptosis of irradiation-damaged SMGCs and reduce irradiation induced cell death. Mechanism studies revealed that tFNAs inhibited cell apoptosis through regulating the Bcl-2/Bax/Caspase-3 signalling pathway and inhibited the release of TNF-α, IL-1β and IL-6 to reduce cell damage caused by inflammation. Animal experiments showed that tFNAs could alleviate irradiation-induced weight loss, increased water intake, decreased saliva production and prolonged salivation lag time and could ameliorate salivary gland damage. tFNAs have a positive effect on alleviating irradiation-induced salivary gland damage and might be a promising agent for the treatment of this disease.
在这项研究中,我们研究了四面体型核酸(tFNAs)在体外和体内辐射诱导唾液腺损伤中的作用。用不同浓度的 tFNAs 处理辐射损伤的颌下腺细胞(SMGCs)。通过 CCK-8 测定法测量细胞活性。通过 Calcein-AM/PI 双重染色检测细胞死亡。通过流式细胞术评估细胞凋亡。通过 Western blot 检测凋亡蛋白和炎症细胞因子的表达。照射 8 周后测量体重、饮水量、唾液流率和滞后时间。通过苏木精-伊红和 Masson 染色评估颌下腺的微观形态变化。通过免疫组织化学染色评估颌下腺的细胞增殖、凋亡和微血管密度。tFNAs 可促进辐射损伤的 SMGC 增殖,抑制细胞凋亡,减少辐射诱导的细胞死亡。机制研究表明,tFNAs 通过调节 Bcl-2/Bax/Caspase-3 信号通路抑制细胞凋亡,并抑制 TNF-α、IL-1β 和 IL-6 的释放,从而减轻炎症引起的细胞损伤。动物实验表明,tFNAs 可减轻辐射诱导的体重减轻、增加饮水量、减少唾液分泌和延长唾液分泌滞后时间,并可改善唾液腺损伤。tFNAs 对缓解辐射诱导的唾液腺损伤有积极作用,可能是治疗这种疾病的有前途的药物。