Chatzopoulou E, Bousaidi N, Guilbert T, Rucher G, Rose J, Germain S, Rouzet F, Chaussain C, Muller L, Gorin C
Université Paris Cité, URP2496 Pathologies, Imagerie et Biothérapies Orofaciales et Plateforme Imagerie du Vivant, Montrouge, France.
AP-HP, Services de médecine bucco-dentaire, FHU DDS-Net, GH Paris Nord et Paris Est, France.
J Dent Res. 2024 Dec;103(13):1392-1402. doi: 10.1177/00220345241271122. Epub 2024 Sep 18.
Regeneration of orofacial tissues is hampered by the lack of adequate vascular supply. Implantation of in vitro engineered, prevascularized constructs has emerged as a strategy to allow the rapid vascularization of the entire graft. Given the angiogenic properties of dental pulp stem cells, we hereby established a preclinical model of prevascularized constructs loaded with stem cells from human exfoliating deciduous teeth (SHED) in a 3-dimensional-printed material and provided a functional analysis of their in vivo angiogenesis, vascular perfusion, and permeability. Three different cell-loaded collagen hydrogels (SHED-human umbilical vein endothelial cell [HUVEC], HUVEC with SHED-conditioned medium, and SHED alone) were cast in polylactic acid (PLA) grids and ectopically implanted in athymic mice. At day 10, in vivo positron emission tomography (PETscan) revealed a significantly increased uptake of radiotracer targeting activated endothelial cells in the SHED-HUVEC group compared to the other groups. At day 30, ex vivo micro-computed tomography imaging confirmed that SHED-HUVEC constructs had a significantly increased vascular volume compared to the other ones. Injection of species-specific lectins analyzed by 2-photon microscopy demonstrated blood perfusion of the engineered human vessels in both prevascularized groups. However, in vivo quantification showed increased vessel density in the SHED-HUVEC group. In addition, coinjection of fluorescent lectin and dextran revealed that prevascularization with SHED prevented vascular leakage, demonstrating the active role of SHED in the maturation of human-engineered microvascular networks. This preclinical study introduces a novel PLA prevascularized and implantable construct, along with an array of imaging techniques, to validate the ability of SHED to promote functional human-engineered vessels, further highlighting the interest of SHED for orofacial tissue engineering. Furthermore, this study validates the use of PETscan for the early detection of in vivo angiogenesis, which may be applied in the clinic to monitor the performance of prevascularized grafts.
口腔颌面部组织的再生因缺乏充足的血管供应而受到阻碍。植入体外构建的预血管化组织已成为一种使整个移植物快速血管化的策略。鉴于牙髓干细胞的血管生成特性,我们在此建立了一种临床前模型,即将人脱落乳牙干细胞(SHED)负载于三维打印材料中构建预血管化组织,并对其体内血管生成、血管灌注和通透性进行功能分析。将三种不同的负载细胞的胶原水凝胶(SHED-人脐静脉内皮细胞[HUVEC]、添加SHED条件培养基的HUVEC以及单独的SHED)浇筑在聚乳酸(PLA)网格中,并异位植入无胸腺小鼠体内。在第10天,体内正电子发射断层扫描(PET扫描)显示,与其他组相比,SHED-HUVEC组中靶向活化内皮细胞的放射性示踪剂摄取显著增加。在第30天,离体微型计算机断层扫描成像证实,与其他组相比,SHED-HUVEC构建体的血管体积显著增加。通过双光子显微镜分析注射的物种特异性凝集素,结果表明两个预血管化组中工程化人类血管均有血液灌注。然而,体内定量分析显示SHED-HUVEC组的血管密度增加。此外,荧光凝集素和葡聚糖的共注射显示,SHED预血管化可防止血管渗漏,这表明SHED在人类工程化微血管网络成熟过程中发挥了积极作用。这项临床前研究引入了一种新型的PLA预血管化可植入构建体以及一系列成像技术,以验证SHED促进功能性人类工程化血管的能力,进一步凸显了SHED在口腔颌面部组织工程中的应用价值。此外,本研究验证了PET扫描在体内血管生成早期检测中的应用,这可能在临床上用于监测预血管化移植物的性能。