Sekiya Naosumi, Matsumiya Goro, Miyagawa Shigeru, Saito Atsuhiro, Shimizu Tatsuya, Okano Teruo, Kawaguchi Naomasa, Matsuura Nariaki, Sawa Yoshiki
Department of Cardiovascular Surgery, Osaka University Graduate School of Medicine, Osaka, Japan.
J Thorac Cardiovasc Surg. 2009 Oct;138(4):985-93. doi: 10.1016/j.jtcvs.2009.02.004.
We previously showed that autologous myoblast sheets constructed with tissue-engineering techniques improved the function of the impaired heart. In this study, we evaluated the effects of layered myoblast sheets to clarify whether increasing the number of sheets provides improvement of cardiac function.
Myoblast sheets were constructed in dishes that release confluent cells from the dish surface via temperature reduction. Sixty infarcted Lewis rats underwent implantation of myoblast sheets on the infarcted area. There were 4 groups (n = 15 in each group): S1: one layer, S3: three layers, S5: five layers, and a sham group. We examined cardiac function by echocardiography and catheterization, mRNA expression by real time reverse-transcriptase polymerase chain reaction, and histology.
The ejection fraction and end-systolic pressure-volume relationship in the S5 and S3 groups were significantly improved. End-diastolic area was significantly reduced in the S5 group. The mRNAs for hepatocyte growth factor, vascular endothelial growth factor, and stromal cell-derived factor-1 were all up-regulated in dose-dependent fashion. On histologic examination, fibrosis was most decreased in S5, and vascular density was increased. Cellular hypertrophy was attenuated in both the S5 and S3 groups. Elastic fibers were massively up-regulated in the infarction and implanted sheets in the S5 and S3 groups, with expression of the elastin gene.
Implantation of three- and five-layered myoblast sheets yields favorable results, with better improvement of cardiac function, induction of angiogenesis, more elastic fibers, and less fibrosis. Thus, layered myoblast sheets, in optimal numbers, may attenuate adverse cardiac remodeling of the infarcted heart.
我们之前表明,利用组织工程技术构建的自体成肌细胞片可改善受损心脏的功能。在本研究中,我们评估了分层成肌细胞片的效果,以阐明增加细胞片层数是否能改善心脏功能。
在通过降温从培养皿表面释放融合细胞的培养皿中构建成肌细胞片。60只梗死的Lewis大鼠在梗死区域植入成肌细胞片。分为4组(每组n = 15):S1组:一层,S3组:三层,S5组:五层,以及假手术组。我们通过超声心动图和导管插入术检查心脏功能,通过实时逆转录聚合酶链反应检测mRNA表达,并进行组织学检查。
S5组和S3组的射血分数和收缩末期压力 - 容积关系显著改善。S5组的舒张末期面积显著减小。肝细胞生长因子、血管内皮生长因子和基质细胞衍生因子 - 1的mRNA均呈剂量依赖性上调。组织学检查显示,S5组纤维化程度降低最明显,血管密度增加。S5组和S3组的细胞肥大均减轻。S5组和S3组梗死区域及植入细胞片中弹性纤维大量上调,伴有弹性蛋白基因表达。
植入三层和五层成肌细胞片可产生良好效果,能更好地改善心脏功能,诱导血管生成,增加弹性纤维,减少纤维化。因此,最佳数量的分层成肌细胞片可能减轻梗死心脏的不良心脏重塑。