Shudo Yasuhiro, Cohen Jeffrey E, MacArthur John W, Goldstone Andrew B, Otsuru Satoru, Trubelja Alen, Patel Jay, Edwards Bryan B, Hung George, Fairman Alexander S, Brusalis Christopher, Hiesinger William, Atluri Pavan, Hiraoka Arudo, Miyagawa Shigeru, Sawa Yoshiki, Woo Y Joseph
1 Department of Cardiothoracic Surgery, Stanford University School of Medicine , Stanford, California.
4 Department of Cardiovascular Surgery, Osaka University Graduate School of Medicine , Osaka, Japan .
Tissue Eng Part A. 2015 Oct;21(19-20):2515-25. doi: 10.1089/ten.TEA.2014.0155. Epub 2015 Sep 18.
There exists a substantial body of work describing cardiac support devices to mechanically support the left ventricle (LV); however, these devices lack biological effects. To remedy this, we implemented a cell sheet engineering approach utilizing chondrocytes, which in their natural environment produce a relatively elastic extracellular matrix (ECM) for a cushioning effect. Therefore, we hypothesized that a chondrocyte cell sheet applied to infarcted and borderzone myocardium will biologically enhance the ventricular ECM and increase elasticity to augment cardiac function in a model of ischemic cardiomyopathy (ICM). Primary articular cartilage chondrocytes of Wistar rats were isolated and cultured on temperature-responsive culture dishes to generate cell sheets. A rodent ICM model was created by ligating the left anterior descending coronary artery. Rats were divided into two groups: cell sheet transplantation (1.0 × 10(7) cells/dish) and no treatment. The cell sheet was placed onto the surface of the heart covering the infarct and borderzone areas. At 4 weeks following treatment, the decreased fibrotic extension and increased elastic microfiber networks in the infarct and borderzone areas correlated with this technology's potential to stimulate ECM formation. The enhanced ventricular elasticity was further confirmed by the axial stretch test, which revealed that the cell sheet tended to attenuate tensile modulus, a parameter of stiffness. This translated to increased wall thickness in the infarct area, decreased LV volume, wall stress, mass, and improvement of LV function. Thus, the chondrocyte cell sheet strengthens the ventricular biomechanical properties by inducing the formation of elastic microfiber networks in ICM, resulting in attenuated myocardial stiffness and improved myocardial function.
有大量工作描述了用于机械支持左心室(LV)的心脏支持装置;然而,这些装置缺乏生物学效应。为了弥补这一点,我们采用了一种细胞片工程方法,利用软骨细胞,软骨细胞在其自然环境中会产生相对有弹性的细胞外基质(ECM)以起到缓冲作用。因此,我们假设将软骨细胞片应用于梗死和边缘区心肌将在生物学上增强心室ECM并增加弹性,从而在缺血性心肌病(ICM)模型中增强心脏功能。分离Wistar大鼠的原代关节软骨细胞,并在温度响应培养皿上培养以生成细胞片。通过结扎左前降支冠状动脉建立啮齿动物ICM模型。将大鼠分为两组:细胞片移植组(1.0×10⁷个细胞/培养皿)和未治疗组。将细胞片放置在覆盖梗死和边缘区的心脏表面。治疗后4周,梗死和边缘区纤维化扩展的减少以及弹性微纤维网络的增加与该技术刺激ECM形成的潜力相关。轴向拉伸试验进一步证实了心室弹性的增强,该试验表明细胞片倾向于降低拉伸模量,拉伸模量是一个刚度参数。这转化为梗死区域壁厚度增加、左心室容积减小、壁应力和质量降低以及左心室功能改善。因此,软骨细胞片通过在ICM中诱导弹性微纤维网络的形成来增强心室生物力学特性,从而导致心肌僵硬度降低和心肌功能改善。