Department of Family Medicine, College of Medicine, Dong-A University, Busan, Korea.
Department of Medicine, College of Medicine, Catholic Kwandong University, Gangneung, Korea.
Cardiovasc Res. 2018 Aug 1;114(10):1400-1409. doi: 10.1093/cvr/cvy086.
In present study, we sought to characterize the angio-vasculogenic property of human adipose mesenchymal stem cells (ASCs) overexpressing dual chemokine GCP-2 and SDF-1α (ASC-G/S) and to determine the therapeutic potential of ASC-G/S in the context of experimental ischaemia.
We generated ASC-G/S line and performed flow cytometry, quantitative (q)-PCR, Matrigel tube formation, Matrigel plug assays, and in vivo therapeutic assays using hind limb ischaemia mouse model. Q-PCR results showed that the representative pro-angiogenic factors were highly upregulated in ASC-G/S compared with ASCs single chemokine overexpressing GCP-2 (ASC-G). In addition, ASC-G/S exhibited high expression of endothelium-specific genes shch as vWF and Flk-1 and showed robust in vitro micro-vascular formation. ASC-G/S was transplanted into ischaemic mouse hind limbs and compared with control groups. ASC-G/S injection prevented limb loss and augmented blood perfusion, suggesting that ASC-G/S enhances neovascularization in hind limb ischaemia. In addition, transplanted ASC-G/S revealed high vasculogenic potential in vivo compared with transplanted ASC-G.
Our data suggest that ASC-G/S has high therapeutic effects on hind limb ischaemia via robust angiogenic and vasculogenic action.
在本研究中,我们试图描述过表达双趋化因子 GCP-2 和 SDF-1α 的人脂肪间充质干细胞(ASCs)的血管生成特性,并确定 ASC-G/S 在实验性缺血情况下的治疗潜力。
我们生成了 ASC-G/S 系,并通过流式细胞术、定量(q)-PCR、Matrigel 管形成、Matrigel plugs 分析以及使用后肢缺血小鼠模型进行体内治疗实验来进行研究。q-PCR 结果表明,与过表达单趋化因子 GCP-2 的 ASC(ASC-G)相比,ASC-G/S 中代表性的促血管生成因子高度上调。此外,ASC-G/S 表现出高表达内皮特异性基因,如 vWF 和 Flk-1,并显示出强大的体外微血管形成能力。将 ASC-G/S 移植到缺血性小鼠后肢,并与对照组进行比较。ASC-G/S 注射可预防肢体丧失并增强血液灌注,表明 ASC-G/S 增强了后肢缺血中的新生血管形成。此外,与移植的 ASC-G 相比,移植的 ASC-G/S 显示出更高的体内血管生成潜力。
我们的数据表明,通过强大的血管生成和血管生成作用,ASC-G/S 对后肢缺血具有很高的治疗效果。