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Local delivery of allogeneic bone marrow and adipose tissue-derived mesenchymal stromal cells for cutaneous wound healing in a porcine model

机译:同种异体骨髓的局部递送和脂肪组织衍生的间充质基质细胞在猪模型中的皮肤伤口愈合

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摘要

Wound healing remains a major challenge in modern medicine. Bone marrow- (BM) and adipose tissue- (AT) derived mesenchymal stromal/stem cells (MSCs) are of great interest for tissue reconstruction due to their unique immunological properties and regenerative potential. The purpose of this study was to characterize BM and AT-MSCs and evaluate their effect when administered in a porcine wound model. MSCs were derived from male Göttingen Minipigs and characterized according to established criteria. Allogeneic BM- or AT-MSCs were administered intradermally (1 × 106 cells) into partial-thickness wounds created on female animals, and covered with Vaseline® gauze or fibrin in a randomized pattern. Animals were euthanized at 7, 10, 14 and 21 days. Tissues were analyzed visually for healing and by microscopic examination for epidermal development and remodelling. Polymerase chain reaction (PCR) was used to detect the presence of male DNA in the specimens. All wounds were healed by 14 days. MSC-injected wounds were associated with improved appearance and faster re-epithelialization compared to saline controls. Evaluation of rete ridge depth and architecture showed that MSC treatment promoted a faster rate of epidermal maturation. Male DNA was detected in all samples at days 7 and 10, suggesting the presence of MSCs. We showed the safety, feasibility and potential efficacy of local injection of allogeneic BM- and AT-MSCs for treatment of wounds in a preclinical model. Our data in this large animal model support the potential use of BM- and AT-MSC for treatment of cutaneous wounds through modulation of healing and epithelialization.
机译:伤口愈合仍然是现代医学中的主要挑战。骨髓(BM)和脂肪组织(AT)来源的间充质基质/干细胞(MSC)由于其独特的免疫学特性和再生潜力而对组织重建非常感兴趣。这项研究的目的是表征BM和AT-MSC并评估在猪伤口模型中给药时的效果。 MSC来自雄性哥廷根小型猪,并根据既定标准对其进行了表征。将同种异体BM-或AT-MSCs皮内注射(1×10 6 细胞)到雌性动物身上形成的局部较厚的伤口中,并以随机方式用Vaseline®纱布或纤维蛋白覆盖。在第7、10、14和21天对动物实施安乐死。目视分析组织的愈合情况,并通过显微镜检查表皮的发育和重塑。聚合酶链反应(PCR)用于检测样品中雄性DNA的存在。所有伤口均治愈14天。与盐水对照组相比,MSC注射的伤口具有改善的外观和更快的上皮再生。对网纹深度和结构的评估表明,MSC处理促进了表皮成熟的更快速度。在第7天和第10天在所有样品中检测到雄性DNA,表明存在MSC。我们在临床前模型中显示了局部注射同种异体BM-和AT-MSC的安全性,可行性和潜在疗效。我们在这个大型动物模型中的数据支持通过调节愈合和上皮形成,将BM-和AT-MSC潜在地用于治疗皮肤伤口。

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