Visone Roberta, Talò Giuseppe, Occhetta Paola, Cruz-Moreira Daniela, Lopa Silvia, Pappalardo Omar Antonio, Redaelli Alberto, Moretti Matteo, Rasponi Marco
Department of Electronics, Information and Bioengineering, Politecnico di Milano, 20133 Milan, Italy.
Cell and Tissue Engineering Lab, IRCCS Istituto Ortopedico Galeazzi, 20161 Milan, Italy.
APL Bioeng. 2018 Oct 29;2(4):046102. doi: 10.1063/1.5037968. eCollection 2018 Dec.
Organs-on-chip technology has recently emerged as a promising tool to generate advanced cardiac tissue models, by recapitulating key physiological cues of the native myocardium. Biochemical, mechanical, and electrical stimuli have been investigated and demonstrated to enhance the maturation of cardiac constructs. However, the combined application of such stimulations on 3D organized constructs within a microfluidic platform was not yet achieved. For this purpose, we developed an innovative microbioreactor designed to provide a uniform electric field and cyclic uniaxial strains to 3D cardiac microtissues, recapitulating the complex electro-mechanical environment of the heart. The platform encompasses a compartment to confine and culture cell-laden hydrogels, a pressure-actuated chamber to apply a cyclic uniaxial stretch to microtissues, and stainless-steel electrodes to accurately regulate the electric field. The platform was exploited to investigate the effect of two different electrical stimulation patterns on cardiac microtissues from neonatal rat cardiomyocytes: a controlled electric field [5 V/cm, or low voltage (LV)] and a controlled current density [74.4 mA/cm, or high voltage (HV)]. Our results demonstrated that LV stimulation enhanced the beating properties of the microtissues. By fully exploiting the platform, we combined the LV electrical stimulation with a physiologic mechanical stretch (10% strain) to recapitulate the key cues of the native cardiac microenvironment. The proposed microbioreactor represents an innovative tool to culture improved miniaturized cardiac tissue models for basic research studies on heart physiopathology and for drug screening.
芯片器官技术最近已成为一种有前景的工具,可通过重现天然心肌的关键生理线索来生成先进的心脏组织模型。生化、机械和电刺激已得到研究,并证明可促进心脏构建体的成熟。然而,尚未实现将这些刺激联合应用于微流控平台内的三维组织化构建体。为此,我们开发了一种创新的微生物反应器,旨在为三维心脏微组织提供均匀的电场和循环单轴应变,重现心脏复杂的机电环境。该平台包括一个用于限制和培养负载细胞水凝胶的隔室、一个用于对微组织施加循环单轴拉伸的压力驱动腔室以及用于精确调节电场的不锈钢电极。利用该平台研究了两种不同电刺激模式对新生大鼠心肌细胞来源的心脏微组织的影响:可控电场[5 V/cm,即低电压(LV)]和可控电流密度[74.4 mA/cm,即高电压(HV)]。我们的结果表明,LV刺激增强了微组织的跳动特性。通过充分利用该平台,我们将LV电刺激与生理机械拉伸(10%应变)相结合,以重现天然心脏微环境的关键线索。所提出的微生物反应器是一种创新工具,用于培养改进的小型化心脏组织模型,用于心脏生理病理学基础研究和药物筛选。