Department of Otolaryngology-Head and Neck Surgery, LSUH-S, Shreveport, Louisiana, U.S.A.
Laryngoscope. 2014 Mar;124(3):642-8. doi: 10.1002/lary.24293. Epub 2013 Jul 19.
OBJECTIVES/HYPOTHESIS: To determine if the intravascular delivery of mesenchymal stem cells improves wound healing and blood perfusion to postischemic cutaneous flap tissues.
Randomized controlled study.
A murine model of a cutaneous flap was created based on the inferior epigastric vessels. Mice (n = 14) underwent 3.5 hours of ischemia followed by reperfusion. Bone marrow stromal cells (BMSCs) 1 × 10(6) were injected intravenously. Wound healing was then assessed measuring percent flap necrosis, flap perfusion, and tensile strength of the flap after a period of 14 days. Localization of BMSCs was determined with radiolabeled and fluorescent labeled BMSCs.
Postischemic cutaneous flap tissues treated with BMSCs demonstrated significantly less necrosis than control flaps (P <0.01). Beginning on postoperative day 5, BMSC-treated flaps demonstrated greater blood perfusion than untreated flaps (P <0.01). Tensile strength of BMSC-treated cutaneous flaps was significantly higher (P <0.01), with a mean strength of 283.4 ± 28.4 N/m than control flaps with a mean of 122.4 ± 23.5 N/m. Radiolabeled BMSCs localized to postischemic flaps compared to untreated tissues (P = 0.001). Fluorescent microscopy revealed incorporation of BMSCs into endothelial and epithelial tissues of postischemic flaps.
This study demonstrates that the intravascular delivery of BMSCs increases wound healing and promotes flap survival following ischemia-reperfusion injury of cutaneous tissue flaps.
目的/假设:确定间质干细胞的血管内输送是否能改善缺血性皮瓣组织的伤口愈合和血液灌注。
随机对照研究。
基于下腹血管创建了一种皮肤瓣的小鼠模型。小鼠(n=14)经历 3.5 小时的缺血,然后再灌注。静脉内注射骨髓基质细胞(BMSCs)1×10(6)个。14 天后,通过测量皮瓣坏死的百分比、皮瓣灌注和皮瓣的拉伸强度来评估伤口愈合。用放射性标记和荧光标记的 BMSC 来确定 BMSC 的定位。
用 BMSC 处理的缺血性皮瓣组织的坏死明显少于对照组(P <0.01)。从术后第 5 天开始,BMSC 处理的皮瓣的血液灌注明显高于未处理的皮瓣(P <0.01)。BMSC 处理的皮瓣的拉伸强度明显更高(P <0.01),平均强度为 283.4±28.4 N/m,而对照组的平均强度为 122.4±23.5 N/m。与未处理的组织相比,放射性标记的 BMSC 定位于缺血性皮瓣(P=0.001)。荧光显微镜显示 BMSC 整合到缺血性皮瓣的内皮和上皮组织中。
这项研究表明,BMSC 的血管内输送可以增加伤口愈合,并促进缺血性皮肤组织瓣再灌注损伤后的皮瓣存活。