Lohana Parkash, Suryaprawira Albert, Woods Emma L, Dally Jordanna, Gait-Carr Edward, Alaidaroos Nadia Y A, Heard Charles M, Lee Kwok Y, Ruge Fiona, Farrier Jeremy N, Enoch Stuart, Caley Matthew P, Peake Matthew A, Davies Lindsay C, Giles Peter J, Thomas David W, Stephens Phil, Moseley Ryan
Disease Mechanisms Group, Oral and Biomedical Sciences, School of Dentistry, College of Biomedical and Life Sciences, Cardiff University, Cardiff CF14 4XY, UK.
Canniesburn Plastic Surgery Unit, Glasgow Royal Infirmary, Glasgow G4 0SF, UK.
Antioxidants (Basel). 2023 Jun 30;12(7):1374. doi: 10.3390/antiox12071374.
Unlike skin, oral mucosal wounds are characterized by rapid healing and minimal scarring, attributable to the "enhanced" healing properties of oral mucosal fibroblasts (OMFs). As oxidative stress is increasingly implicated in regulating wound healing outcomes, this study compared oxidative stress biomarker and enzymic antioxidant profiles between patient-matched oral mucosal/skin tissues and OMFs/skin fibroblasts (SFs) to determine whether superior oral mucosal antioxidant capabilities and reduced oxidative stress contributed to these preferential healing properties. Oral mucosa and skin exhibited similar patterns of oxidative protein damage and lipid peroxidation, localized within the lamina propria/dermis and oral/skin epithelia, respectively. SOD1, SOD2, SOD3 and catalase were primarily localized within epithelial tissues overall. However, SOD3 was also widespread within the lamina propria localized to OMFs, vasculature and the extracellular matrix. OMFs were further identified as being more resistant to reactive oxygen species (ROS) generation and oxidative DNA/protein damage than SFs. Despite histological evaluation suggesting that oral mucosa possessed higher SOD3 expression, this was not fully substantiated for all OMFs examined due to inter-patient donor variability. Such findings suggest that enzymic antioxidants have limited roles in mediating privileged wound healing responses in OMFs, implying that other non-enzymic antioxidants could be involved in protecting OMFs from oxidative stress overall.
与皮肤不同,口腔黏膜伤口的特点是愈合迅速且瘢痕形成极少,这归因于口腔黏膜成纤维细胞(OMF)具有“增强的”愈合特性。由于氧化应激越来越多地与调节伤口愈合结果有关,本研究比较了患者匹配的口腔黏膜/皮肤组织以及OMF/皮肤成纤维细胞(SF)之间的氧化应激生物标志物和酶促抗氧化剂谱,以确定口腔黏膜优越的抗氧化能力和氧化应激的降低是否促成了这些优先愈合特性。口腔黏膜和皮肤分别在固有层/真皮层以及口腔/皮肤上皮中呈现出相似的氧化蛋白质损伤和脂质过氧化模式。超氧化物歧化酶1(SOD1)、超氧化物歧化酶2(SOD2)、超氧化物歧化酶3(SOD3)和过氧化氢酶总体上主要定位于上皮组织。然而,SOD3在定位于OMF、脉管系统和细胞外基质的固有层中也广泛存在。进一步研究发现,与SF相比,OMF对活性氧(ROS)生成以及氧化DNA/蛋白质损伤更具抗性。尽管组织学评估表明口腔黏膜具有更高的SOD3表达,但由于患者间供体的变异性,在所有检测的OMF中这一点并未得到充分证实。这些发现表明,酶促抗氧化剂在介导OMF的特殊伤口愈合反应中作用有限,这意味着其他非酶促抗氧化剂可能总体上参与保护OMF免受氧化应激。