Hong Yoonki, Kim You-Sun, Hong Seok-Ho, Oh Yeon-Mok
Department of Internal Medicine, Kangwon National University Hospital, Chuncheon, Korea.
Asan Institute for Life Sciences, Department of Pulmonary and Critical Care Medicine, University of Ulsan College of Medicine, Seoul, Korea.
Exp Mol Med. 2016 Oct 21;48(10):e266. doi: 10.1038/emm.2016.93.
There is no therapy currently available that influences the natural history of disease progression in patients with chronic obstructive pulmonary disease (COPD). Although stem cell therapy is considered a potential therapeutic option in COPD, there are no clinical trials proving definitive therapeutic effects in patients with COPD. Recently, it was reported that pioglitazone might potentiate the therapeutic effects of stem cells in patients with heart or liver disease. To test the capacity of pioglitazone pretreatment of stem cells for emphysema repair, we evaluated the therapeutic effects of pioglitazone-pretreated human adipose-derived mesenchymal stem cells (ASCs) on elastase-induced or cigarette smoke-induced emphysema in mice. We also investigated the mechanisms of action of pioglitazone-pretreated ASCs. Pioglitazone-pretreated ASCs had a more potent therapeutic effect than non-pretreated ASCs in the repair of both elastase-induced and smoke-induced emphysema models (mean linear intercept, 78.1±2.5 μm vs 83.2±2.6 μm in elastase models and 75.6±1.4 μm vs 80.5±3.2 μm in smoke models, P<0.05). Furthermore, we showed that pioglitazone-pretreated ASCs increased vascular endothelial growth factor (VEGF) production both in vitro and in mouse lungs in the smoke-induced emphysema model. Pioglitazone-pretreated ASCs may have more potent therapeutic effects than non-pretreated ASCs in emphysema mouse models.
目前尚无能够影响慢性阻塞性肺疾病(COPD)患者疾病进展自然史的治疗方法。尽管干细胞疗法被认为是COPD的一种潜在治疗选择,但尚无临床试验证明其对COPD患者有确切的治疗效果。最近,有报道称吡格列酮可能增强干细胞对心脏病或肝病患者的治疗效果。为了测试吡格列酮预处理干细胞对肺气肿修复的能力,我们评估了吡格列酮预处理的人脂肪间充质干细胞(ASC)对弹性蛋白酶诱导或香烟烟雾诱导的小鼠肺气肿的治疗效果。我们还研究了吡格列酮预处理的ASC的作用机制。在弹性蛋白酶诱导和烟雾诱导的肺气肿模型修复中,吡格列酮预处理的ASC比未预处理的ASC具有更强的治疗效果(弹性蛋白酶模型中平均线性截距分别为78.1±2.5μm和83.2±2.6μm,烟雾模型中分别为75.6±1.4μm和80.5±3.2μm,P<0.05)。此外,我们发现在烟雾诱导的肺气肿模型中,吡格列酮预处理的ASC在体外和小鼠肺中均增加了血管内皮生长因子(VEGF)的产生。在肺气肿小鼠模型中,吡格列酮预处理的ASC可能比未预处理的ASC具有更强的治疗效果。