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使用仿生心脏组织模型(BCTM)进行血液动力学刺激可增强人诱导多能干细胞衍生的心肌细胞的成熟。

Hemodynamic Stimulation Using the Biomimetic Cardiac Tissue Model (BCTM) Enhances Maturation of Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes.

机构信息

Division of Cardiovascular Disease, Departments of Medicine and Biomedical Engineering, University of Alabama at Birmingham, Birmingham, Alabama, USA,

Department of Biomedical Engineering, University of Alabama at Birmingham, Birmingham, Alabama, USA.

出版信息

Cells Tissues Organs. 2018;206(1-2):82-94. doi: 10.1159/000496934. Epub 2019 Mar 6.

Abstract

Human induced pluripotent stem cell (hiPSC)-derived cardio-myocytes (hiPSC-CMs) hold great promise for cardiovascular disease modeling and regenerative medicine. However, these cells are both structurally and functionally -immature, primarily due to their differentiation into cardiomyocytes occurring under static culture which only reproduces biomolecular cues and ignores the dynamic hemo-dynamic cues that shape early and late heart development during cardiogenesis. To evaluate the effects of hemodynamic stimuli on hiPSC-CM maturation, we used the biomimetic cardiac tissue model to reproduce the hemodynamics and pressure/volume changes associated with heart development. Following 7 days of gradually increasing stimulation, we show that hemodynamic loading results in (a) enhanced alignment of the cells and extracellular matrix, (b) significant increases in genes associated with physiological hypertrophy, (c) noticeable changes in sarcomeric organization and potential changes to cellular metabolism, and (d) a significant increase in fractional shortening, suggestive of a positive force frequency response. These findings suggest that culture of hiPSC-CMs under conditions that accurately reproduce hemodynamic cues results in structural orga-nization and molecular signaling consistent with organ growth and functional maturation.

摘要

人诱导多能干细胞(hiPSC)衍生的心肌细胞(hiPSC-CMs)在心血管疾病建模和再生医学方面具有巨大的应用潜力。然而,这些细胞在结构和功能上都不成熟,主要是由于它们在静态培养条件下分化为心肌细胞,这种培养方式仅能复制生物分子信号,而忽略了在心脏发生过程中塑造早期和晚期心脏发育的动态血液动力学信号。为了评估血液动力学刺激对 hiPSC-CM 成熟的影响,我们使用仿生心脏组织模型来模拟与心脏发育相关的血液动力学和压力/容积变化。经过 7 天逐渐增加的刺激,我们发现血液动力学负荷导致:(a)细胞和细胞外基质的排列增强;(b)与生理肥大相关的基因显著增加;(c)肌节组织的明显变化和细胞代谢的潜在变化;(d)分数缩短显著增加,提示存在正向力频率反应。这些发现表明,在能够准确复制血液动力学信号的条件下培养 hiPSC-CMs 会导致结构组织和分子信号与器官生长和功能成熟一致。

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