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MSC 移植联合 netrin-1 可改善大鼠后肢缺血模型中的新生血管形成。

Transplantation of MSCs in combination with netrin-1 improves neoangiogenesis in a rat model of hind limb ischemia.

机构信息

Department of Endocrinology, Nanjing First Hospital Affiliated to Nanjing Medical University, Nanjing, 210006, China.

出版信息

J Surg Res. 2011 Mar;166(1):162-9. doi: 10.1016/j.jss.2009.08.031. Epub 2009 Sep 23.

Abstract

BACKGROUND

Similar to the neural network, the vascular network is formed from central axial structures that send sprouts along predetermined trajectories to their distal destinations. Indeed, recent evidence indicates that neuronal guidance factors and their receptors function as angiogenic regulators. As neural guidance cues, netrin-1 is the most extensively studied gene in the field of angiogenesis. Despite achieving some advances in mesenchymal stem cell (MSC) therapy in angiogenesis, there are still a certain number of patients who fail to respond to cell therapy. Thus, a novel therapeutic strategy to enhance the angiogenic property of transplanted cells is desirable. This study examined the impact of combined netrin-1 protein and MSC implantation on therapeutic angiogenesis in a rat model of hind limb ischemia.

METHODS

Hind limb ischemic rats (n = 24) were divided randomly into four groups (six rats per group): control group (0.05 mL saline); netrin-1 group (1 μg netrin-1 dissolved in 0.05 mL saline); MSC group (1 × 10(6) MSCs); and netrin-1/MSCs group (1 μg netrin-1 combined with MSCs). Netrin-1 and/or MSCs were injected directly into the muscle of the ischemic limb. Gross appearance of ischemic limb, collateral vessel formation, and vascular endothelial growth factor (VEGF) level were assessed 28 d after treatment.

RESULTS

The results showed that pretreatment of MSCs with a recombinant netrin-1 protein markedly augmented the angiographic score and capillary density, improved function of the ischemic limb, and increased levels of VEGF in the plasma and damaged tissues. Further studies assaying the cell migration and network formation suggested that netrin-1 promoted MSC migration and enhanced its ability to participate in tube formation.

CONCLUSIONS

These results demonstrated that transplantation of MSCs pretreated with netrin-1 protein significantly improved the therapeutic effect of MSCs and, therefore, may provide a novel therapeutic approach for ischemic disease.

摘要

背景

类似于神经网络,血管网络是由中央轴向结构形成的,这些结构沿着预定的轨迹发出芽,到达它们的远端目的地。事实上,最近的证据表明,神经元导向因子及其受体作为血管生成调节剂发挥作用。作为神经导向线索,轴突导向因子 netrin-1 是血管生成领域研究最多的基因。尽管在血管生成的间充质干细胞(MSC)治疗方面取得了一些进展,但仍有一定数量的患者对细胞治疗无反应。因此,需要一种新的治疗策略来增强移植细胞的血管生成特性。本研究在大鼠后肢缺血模型中,研究了 netrin-1 蛋白与 MSC 联合植入对治疗性血管生成的影响。

方法

将后肢缺血大鼠(n = 24)随机分为四组(每组 6 只):对照组(0.05 mL 生理盐水);netrin-1 组(1 μg netrin-1 溶解于 0.05 mL 生理盐水);MSC 组(1×106 MSC);netrin-1 / MSC 组(1 μg netrin-1 与 MSC 联合)。将 netrin-1 和/或 MSC 直接注射到缺血肢体的肌肉中。治疗 28 天后评估缺血肢体的大体外观、侧支血管形成和血管内皮生长因子(VEGF)水平。

结果

结果表明,用重组 netrin-1 蛋白预处理 MSC 可显著提高血管造影评分和毛细血管密度,改善缺血肢体功能,并增加血浆和损伤组织中的 VEGF 水平。进一步的细胞迁移和网络形成研究表明,netrin-1 促进 MSC 迁移并增强其参与管形成的能力。

结论

这些结果表明,用 netrin-1 蛋白预处理的 MSC 移植可显著改善 MSC 的治疗效果,因此可能为缺血性疾病提供一种新的治疗方法。

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