Radiodiagnostic Institute, University Hospital Ostrava, Ostrava, Czech Republic.
Department of Deputy Director of Science and Research, University Hospital Ostrava, Ostrava, Czech Republic.
Med Sci Monit. 2018 Jan 26;24:511-522. doi: 10.12659/msm.905442.
BACKGROUND Paracrine factors secreted by adipose-derived stem cells can be captured, fractionated, and concentrated to produce therapeutic factor concentrate (TFC). The present study examined whether TFC effects could be enhanced by combining TFC with a biological matrix to provide sustained release of factors in the target region. MATERIAL AND METHODS Unilateral hind limb ischemia was induced in rabbits. Ischemic limbs were injected with either placebo control, TFC, micronized small intestinal submucosa tissue (SIS), or TFC absorbed to SIS. Blood flow in both limbs was assessed with laser Doppler perfusion imaging. Tissues harvested at Day 48 were assessed immunohistochemically for vessel density; in situ hybridization and quantitative real-time PCR were employed to determine miR-126 expression. RESULTS LDP ratios were significantly elevated, compared to placebo control, on day 28 in all treatment groups (p=0.0816, p=0.0543, p=0.0639, for groups 2-4, respectively) and on day 36 in the TFC group (p=0.0866). This effect correlated with capillary density in the SIS and TFC+SIS groups (p=0.0093 and p=0.0054, respectively, compared to placebo). A correlation was observed between miR-126 levels and LDP levels at 48 days in SIS and TFC+SIS groups. CONCLUSIONS A single bolus administration of TFC and SIS had early, transient effects on reperfusion and promotion of ischemia repair. The effects were not additive. We also discovered that TFC modulated miR-126 levels that were expressed in cell types other than endothelial cells. These data suggested that TFC, alone or in combination with SIS, may be a potent therapy for patients with CLI that are at risk of amputation.
脂肪来源的干细胞分泌的旁分泌因子可以被捕获、分离和浓缩,以产生治疗因子浓缩物(TFC)。本研究旨在探讨 TFC 与生物基质结合是否可以增强 TFC 的效果,从而在靶区提供因子的持续释放。
在兔的单侧后肢缺血模型中,将安慰剂对照、TFC、微粉化的小肠黏膜下层组织(SIS)或 TFC 吸收到 SIS 中注射到缺血肢体。用激光多普勒灌注成像评估两条肢体的血流。在第 48 天,通过免疫组织化学评估血管密度;通过原位杂交和定量实时 PCR 来确定 miR-126 的表达。
与安慰剂对照组相比,所有治疗组在第 28 天(分别为 p=0.0816、p=0.0543、p=0.0639)和第 36 天的 TFC 组(p=0.0866)的 LDP 比值显著升高。这种效果与 SIS 和 TFC+SIS 组中的毛细血管密度相关(与安慰剂相比,分别为 p=0.0093 和 p=0.0054)。在 SIS 和 TFC+SIS 组中,miR-126 水平与 48 天时的 LDP 水平之间存在相关性。
TFC 和 SIS 的单次推注对再灌注和促进缺血修复有早期、短暂的作用。这种效果不是累加的。我们还发现,TFC 调节了除内皮细胞以外的细胞类型中表达的 miR-126 水平。这些数据表明,TFC 单独或与 SIS 联合使用可能是一种有效的 CLI 患者治疗方法,这些患者有截肢的风险。