首页> 美国卫生研究院文献>Tissue Engineering. Part A >A Tissue-Engineered Chondrocyte Cell Sheet Induces Extracellular Matrix Modification to Enhance Ventricular Biomechanics and Attenuate Myocardial Stiffness in Ischemic Cardiomyopathy
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A Tissue-Engineered Chondrocyte Cell Sheet Induces Extracellular Matrix Modification to Enhance Ventricular Biomechanics and Attenuate Myocardial Stiffness in Ischemic Cardiomyopathy

机译:组织工程化的软骨细胞片诱导细胞外基质修饰以增强缺血性心肌病的心室生物力学和减轻心肌的僵硬。

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摘要

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 × 107 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.
机译:存在大量的工作,描述了心脏支撑装置以机械方式支撑左心室(LV)。然而,这些装置缺乏生物学效应。为了解决这个问题,我们实施了一种利用软骨细胞的细胞表工程方法,该细胞在自然环境中产生相对弹性的细胞外基质(ECM)以产生缓冲作用。因此,我们假设在缺血性心肌病(ICM)模型中,将一种软骨细胞片应用于梗塞和边界区的心肌会生物增强心室ECM并增加弹性以增强心脏功能。分离Wistar大鼠的原发性软骨软骨细胞,并在温度响应性培养皿上培养以产生细胞片。通过结扎左冠状动脉前降支,建立啮齿动物ICM模型。大鼠分为两组:细胞片移植(1.0××10 7 细胞/皿)和不治疗。将细胞片放在覆盖梗塞和边界带区域的心脏表面上。治疗后第4周,梗死区和边界区的纤维化延伸减少,弹性微纤维网络增加,与该技术刺激ECM形成的潜力有关。通过轴向拉伸试验进一步证实了增强的心室弹性,这表明细胞片倾向于减弱拉伸模量,这是刚性的参数。这导致梗死区域壁厚增加,LV体积减少,壁应力,肿块和LV功能改善。因此,软骨细胞片通过诱导ICM中的弹性微纤维网络的形成来增强心室的生物力学性能,从而减弱了心肌的硬度并改善了心肌的功能。

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