Department of Biomedicine, University of Bergen, Bergen, Norway.
Department of Clinical Dentistry, University of Bergen, Bergen, Norway.
Eur J Oral Sci. 2024 Aug;132(4):e13006. doi: 10.1111/eos.13006. Epub 2024 Jul 11.
Lymphatics are involved in the resolution of inflammation and wound healing, but their role in the oral wound healing process after tooth extraction has never been investigated. We therefore sought to evaluate the healing process following the extraction of maxillary molars in two transgenic mouse models: K14-VEGFR3-Ig mice, which lack initial mucosal lymphatic vessels, and K14-VEGFC mice, which have hyperplastic mucosal lymphatics. Maxillary molars were extracted from both transgenic mouse types and their corresponding wild-type (WT) controls. Mucosal and alveolar bone healing were evaluated. A delayed epithelialization and bone regeneration were observed in K14-VEGFR3-Ig mice compared with their WT littermates. The hampered wound closure was accompanied by decreased levels of epidermal growth factor (EGF) and persistent inflammation, characterized by infiltrates of immune cells and elevated levels of pro-inflammatory markers in the wounds. Hyperplastic mucosal lymphatics did not enhance the healing process after tooth extraction in K14-VEGFC mice. The findings indicate that initial mucosal lymphatics play a major role in the initial phase of the oral wound healing process.
淋巴管参与炎症和伤口愈合的过程,但它们在拔牙后口腔伤口愈合过程中的作用尚未被研究过。因此,我们试图在两种转基因小鼠模型中评估上颌磨牙拔除后的愈合过程:K14-VEGFR3-Ig 小鼠,其缺乏初始黏膜淋巴管,以及 K14-VEGFC 小鼠,其具有增生的黏膜淋巴管。从这两种转基因小鼠类型及其相应的野生型(WT)对照中提取上颌磨牙。评估黏膜和牙槽骨的愈合情况。与 WT 同窝仔相比,K14-VEGFR3-Ig 小鼠的上皮化和骨再生出现延迟。阻碍的伤口闭合伴随着表皮生长因子(EGF)水平降低和持续的炎症,特征是伤口中有免疫细胞浸润和促炎标志物水平升高。在 K14-VEGFC 小鼠中,增生的黏膜淋巴管并没有促进拔牙后的愈合过程。研究结果表明,初始黏膜淋巴管在上颌伤口愈合过程的初始阶段起着主要作用。