Shigemura Norihisa, Okumura Meinoshin, Mizuno Shinya, Imanishi Yukiko, Matsuyama Akifumi, Shiono Hiroyuki, Nakamura Toshikazu, Sawa Yoshiki
Division of Cardiothoracic Surgery, Department of Surgery, Course of Advanced Medicine, Medical Center for Translational Research, Osaka University Graduate School of Medicine, Osaka, Japan.
Am J Respir Crit Care Med. 2006 Dec 1;174(11):1199-205. doi: 10.1164/rccm.200603-406OC. Epub 2006 Sep 28.
Hepatocyte growth factor (HGF) is a potent regenerative factor generated after a lung injury, and HGF supplementation after surgical reduction has been shown to enhance compensatory growth in remnant lungs and improve pathophysiologic conditions in a rat model of emphysema. Adipose tissue-derived stromal cells (ASCs) produce a large amount of angiogenic factors, including HGF. After lung volume reduction surgery (LVRS), we treated rats by implanting HGF-secreting ASCs with a scaffold onto the remnant lung tissue to determine the usefulness of this technique for treating respiratory dysfunction.
Cells were isolated from rat inguinal adipose tissue and characterized by flow cytometry. ASCs were cultured on a polyglycolic acid felt sheet as a sealant material, and were shown to secrete significantly greater amounts of HGF than other angiogenic factors. Next, ASCs on polyglycolic acid felt sheets were used to cover the cut edge of the remaining lungs after LVRS for emphysema in rats. One week after implantation of the ASCs, both alveolar and vascular regeneration were significantly accelerated as compared with the rats that underwent LVRS alone. Consequently, gas exchange and exercise tolerance were also significantly restored, with these good results persisting for more than 1 mo.
The present findings demonstrate the therapeutic potential of cell therapy using ASCs with a scaffold for selective delivery of HGF to remnant lungs, which resulted in enhancement of compensatory growth, after surgical resection. This approach may provide a new strategy for lung tissue engineering to improve LVRS outcome.
肝细胞生长因子(HGF)是肺损伤后产生的一种强效再生因子,手术减容后补充HGF已被证明可增强残余肺的代偿性生长,并改善肺气肿大鼠模型的病理生理状况。脂肪组织来源的基质细胞(ASC)可产生大量包括HGF在内的血管生成因子。在肺减容手术(LVRS)后,我们通过将分泌HGF的ASC与支架一起植入大鼠残余肺组织来进行治疗,以确定该技术治疗呼吸功能障碍的有效性。
从大鼠腹股沟脂肪组织中分离细胞,并通过流式细胞术进行鉴定。将ASC培养在聚乙醇酸毡片上作为密封材料,结果显示其分泌的HGF量显著高于其他血管生成因子。接下来,将聚乙醇酸毡片上的ASC用于覆盖大鼠肺气肿LVRS后剩余肺的切缘。与仅接受LVRS的大鼠相比,植入ASC一周后,肺泡和血管再生均显著加速。因此,气体交换和运动耐力也显著恢复,且这些良好结果持续超过1个月。
本研究结果表明,使用ASC与支架进行细胞治疗具有治疗潜力,可将HGF选择性递送至残余肺,从而在手术切除后增强代偿性生长。这种方法可能为肺组织工程提供一种新策略,以改善LVRS的疗效。