National Engineering Laboratory for Oral Regenerative Medicine & Engineering Research Center of Oral Translational Medicine, Ministry of Education & State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases & Department of Pediatric Dentistry, West China School of Stomatology, Sichuan University, Chengdu, China.
School of Medicine, Nankai University, Tianjin, China.
Int J Oral Sci. 2023 Feb 16;15(1):10. doi: 10.1038/s41368-023-00217-4.
Xenogenic organ transplantation has been considered the most promising strategy in providing possible substitutes with the physiological function of the failing organs as well as solving the problem of insufficient donor sources. However, the xenograft, suffered from immune rejection and ischemia-reperfusion injury (IRI), causes massive reactive oxygen species (ROS) expression and the subsequent cell apoptosis, leading to the xenograft failure. Our previous study found a positive role of PPAR-γ in anti-inflammation through its immunomodulation effects, which inspires us to apply PPAR-γ agonist rosiglitazone (RSG) to address survival issue of xenograft with the potential to eliminate the excessive ROS. In this study, xenogenic bioroot was constructed by wrapping the dental follicle cells (DFC) with porcine extracellular matrix (pECM). The hydrogen peroxide (HO)-induced DFC was pretreated with RSG to observe its protection on the damaged biological function. Immunoflourescence staining and transmission electron microscope were used to detect the intracellular ROS level. SD rat orthotopic transplantation model and superoxide dismutase 1 (SOD1) knockout mice subcutaneous transplantation model were applied to explore the regenerative outcome of the xenograft. It showed that RSG pretreatment significantly reduced the adverse effects of HO on DFC with decreased intracellular ROS expression and alleviated mitochondrial damage. In vivo results confirmed RSG administration substantially enhanced the host's antioxidant capacity with reduced osteoclasts formation and increased periodontal ligament-like tissue regeneration efficiency, maximumly maintaining the xenograft function. We considered that RSG preconditioning could preserve the biological properties of the transplanted stem cells under oxidative stress (OS) microenvironment and promote organ regeneration by attenuating the inflammatory reaction and OS injury.
异种器官移植被认为是提供具有衰竭器官生理功能的可能替代品以及解决供体来源不足问题的最有前途的策略。然而,异种移植物受到免疫排斥和缺血再灌注损伤(IRI)的影响,导致大量活性氧(ROS)表达和随后的细胞凋亡,导致异种移植物衰竭。我们之前的研究发现 PPAR-γ 通过其免疫调节作用在抗炎中发挥积极作用,这启发我们应用 PPAR-γ 激动剂罗格列酮(RSG)来解决异种移植物的生存问题,并有潜力消除过多的 ROS。在这项研究中,我们通过用猪细胞外基质(pECM)包裹牙滤泡细胞(DFC)构建了异种生物根。用 H2O2(HO)预处理诱导的 DFC,观察 RSG 对受损生物功能的保护作用。用免疫荧光染色和透射电子显微镜检测细胞内 ROS 水平。SD 大鼠原位移植模型和超氧化物歧化酶 1(SOD1)敲除小鼠皮下移植模型用于探索异种移植物的再生结果。结果表明,RSG 预处理可显著减轻 HO 对 DFC 的不良影响,降低细胞内 ROS 表达,减轻线粒体损伤。体内结果证实,RSG 给药可显著增强宿主的抗氧化能力,减少破骨细胞形成,增加牙周韧带样组织再生效率,最大程度地维持异种移植物功能。我们认为,RSG 预处理可以在氧化应激(OS)微环境下保存移植干细胞的生物学特性,并通过减轻炎症反应和 OS 损伤来促进器官再生。