U.S. Army Institute of Surgical Research, Combat Trauma and Burn Injury Research, JBSA Fort Sam Houston, TX, USA.
U.S. Army Institute of Surgical Research, Coagulation and Blood Research, JBSA Fort Sam Houston, TX, USA.
Acta Biomater. 2019 Mar 15;87:76-87. doi: 10.1016/j.actbio.2019.01.039. Epub 2019 Jan 18.
Despite great advances in skin wound care utilizing grafting techniques, the resulting severe scarring, deformity and ineffective vascularization remains a challenge. Alternatively, tissue engineering of new skin using patient-derived stem cells and scaffolding materials promises to greatly increase the functional and aesthetic outcome of skin wound healing. This work focused on the optimization of a polyethylene glycol modified (PEGylated) platelet-rich plasma (PRP) hydrogel for the protracted release of cytokines, growth factors, and signaling molecules and also the delivery of a provisional physical framework for stem cell angiogenesis. Freshly collected whole blood was utilized to synthesize PEGylated PRP hydrogels containing platelet concentrations ranging from 0 to 200,000 platelets/µl. Hydrogels were characterized using thromboelastography and impedance aggregometry for platelet function and were visualized using scanning electron microscopy. To assess the effects of PEGylated PRP hydrogels on cells, PRP solutions were seeded with human adipose-derived stem cells (ASCs) prior to gelation. Following 14 days of incubation in vitro, increased platelet concentrations resulted in higher ASC proliferation and vascular gene and protein expression (assessed via RT-PCR, ELISA, and immunochemistry). Using a rat skin excision model, wounds treated with PRP + ASC hydrogels increased the number of vessels in the wound by day 8 (80.2 vs. 62.6 vessels/mm) compared to controls. In conclusion, the proposed PEGylated PRP hydrogel promoted both in vitro and transient in vivo angiogenesis of ASCs for improved wound healing. STATEMENT OF SIGNIFICANCE: Our findings support an innovative means of cellular therapy intervention to improve surgical wound healing in a normal wound model. ASCs seeded within PEGylated PRP could be an efficacious and completely autologous therapy for treating patients who have poorly healing wounds caused by vascular insufficiency, previous irradiation, or full-thickness burns. Because wound healing is a dynamic and complex process, the application of more than one growth factor with ASCs demonstrates an advantageous way of improving healing.
尽管在皮肤伤口护理方面取得了很大进展,采用了移植物技术,但由此导致的严重瘢痕形成、畸形和血管化效果不佳仍然是一个挑战。另一方面,利用患者来源的干细胞和支架材料进行组织工程学构建新皮肤,有望极大地提高皮肤伤口愈合的功能和美观效果。本研究工作重点优化了一种聚乙二醇修饰(PEGylated)的富含血小板血浆(PRP)水凝胶,以实现细胞因子、生长因子和信号分子的持续释放,并为干细胞血管生成提供临时物理框架。使用新鲜采集的全血合成了 PRP 水凝胶,其中血小板浓度范围为 0 至 200,000 个血小板/µl。使用血栓弹性图和阻抗聚集度测定法对血小板功能进行了水凝胶特性分析,并通过扫描电子显微镜进行了可视化观察。为了评估 PEGylated PRP 水凝胶对细胞的影响,将 PRP 溶液与人类脂肪来源的干细胞(ASCs)一起接种,然后凝胶化。在体外孵育 14 天后,随着血小板浓度的增加,ASCs 的增殖以及血管生成基因和蛋白表达(通过 RT-PCR、ELISA 和免疫化学测定)也随之增加。在大鼠皮肤切除模型中,与对照组相比,用 PRP+ASC 水凝胶处理的伤口在第 8 天增加了伤口中的血管数量(80.2 个/毫米与 62.6 个/毫米)。总之,所提出的 PEGylated PRP 水凝胶促进了 ASC 的体外和短暂体内血管生成,从而改善了伤口愈合。研究意义:我们的研究结果为改善正常伤口模型中的外科伤口愈合提供了一种创新的细胞治疗干预手段。在 PEGylated PRP 中接种的 ASC 可以作为一种有效的完全自体疗法,用于治疗因血管功能不全、先前的辐射或全层烧伤导致伤口愈合不良的患者。由于伤口愈合是一个动态且复杂的过程,因此将一种以上的生长因子与 ASC 联合应用展示了改善愈合的有利方法。