Histological Evidence for Therapeutic Induction of Angiogenesis Using Mast Cells and Platelet-Rich Plasma within A Bioengineered Scaffold following Rat Hindlimb Ischemia

A. Karimi, R. Shahrooz, Rahim Hobbenagh, R. Mohammadi, N. Delirezh, S. Amani, J. Garssen, E. Mortaz, I. M Adcock
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引用次数: 5

Abstract

Objective Peripheral arterial disease results from obstructed blood flow in arteries and increases the risk of amputation in acute cases. Therapeutic angiogenesis using bioengineered tissues composed of a chitosan scaffold that was enriched with mast cells (MCs) and/or platelet-rich plasma (PRP) was used to assess the formation of vascular networks and subsequently improved the functional recovery following hindlimb ischemia. This study aimed to find an optimal approach for restoring local vascularization. Materials and Methods In this experimental study, thirty rats were randomly divided into six experimental groups: a. Ischemic control group with right femoral artery transection, b. Ischemia with phosphate-buffered saline (PBS) control group, c. Ischemia with chitosan scaffold, d. Ischemia with chitosan and MCs, e. Ischemia with chitosan and PRP, and f. Ischemia with chitosan, PRP, and MCs. The left hind limbs served as non-ischemic controls. The analysis of capillary density, arterial diameter, histomorphometric analysis and immunohistochemistry at the transected locations and in gastrocnemius muscles was performed. Results The group treated with chitosan/MC significantly increased capillary density and the mean number of large blood vessels at the site of femoral artery transection compared with other experimental groups (P<0.05). The treatment with chitosan/MC also significantly increased the muscle fiber diameter and the capillary-to-muscle fiber ratio in gastrocnemius muscles compared with all other ischemic groups (P<0.05). Conclusion These findings suggested that chitosan and MCs together could offer a new approach for the therapeutic induction of angiogenesis in cases of peripheral arterial diseases.
生物工程支架内使用肥大细胞和富血小板血浆诱导大鼠后肢缺血后血管生成的组织学证据
目的外周动脉疾病是由动脉血流阻塞引起的,增加了急性病例截肢的风险。利用富含肥大细胞(MCs)和/或富血小板血浆(PRP)的壳聚糖支架组成的生物工程组织进行治疗性血管生成,以评估血管网络的形成,并随后改善后肢缺血后的功能恢复。本研究旨在寻找恢复局部血管化的最佳方法。材料与方法将30只大鼠随机分为6个实验组:a.右股动脉缺血对照组,b.磷酸缓冲盐水(PBS)缺血对照组,c.壳聚糖支架缺血组,d.壳聚糖和MCs缺血组,e.壳聚糖和PRP缺血组,f.壳聚糖、PRP和MCs缺血组。左后肢作为非缺血对照。对横断部位及腓肠肌的毛细血管密度、动脉直径、组织形态学分析及免疫组织化学进行分析。结果与其他实验组相比,壳聚糖/MC组大鼠股动脉横断部位毛细血管密度和平均大血管数显著增加(P<0.05)。壳聚糖/MC组与其他缺血组相比,显著增加了腓肠肌肌纤维直径和毛细血管/肌纤维比(P<0.05)。结论壳聚糖与MCs联合应用可为外周动脉病变诱导血管生成提供新的治疗途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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