Effects of Physiologic Mechanical Stimulation on Embryonic Chick Cardiomyocytes Using a Microfluidic Cardiac Cell Culture Model

• Published in: Analytical chemistry (Washington) 2015-02, Vol.87 (4), p.2107-2113
• Main Authors: Nguyen, Mai-Dung, Tinney, Joseph P, Ye, Fei, Elnakib, Ahmed A, Yuan, Fangping, El-Baz, Ayman, Sethu, Palaniappan, Keller, Bradley B, Giridharan, Guruprasad A
• Format: Article
• Language: English
• Subjects: Animals; Biochemistry; Biotechnology; Calcium; Cardiomyocytes; Cardiotonic Agents - pharmacology; Cell culture; Cell Culture Techniques - instrumentation; Cells, Cultured; Chick Embryo - cytology; Chicks; Cues; Equipment Design; Gene Expression; Handling; Isoproterenol - pharmacology; Mechanical Phenomena; Microfluidic Analytical Techniques - instrumentation; Microfluidics; Myocytes, Cardiac - cytology; Myocytes, Cardiac - drug effects; Myocytes, Cardiac - metabolism; Protein Biosynthesis; Protein synthesis; Stimulation; Tissue engineering
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/ac503716z

Hemodynamic mechanical cues play a critical role in the early development and functional maturation of cardiomyocytes (CM). Therefore, tissue engineering approaches that incorporate immature CM into functional cardiac tissues capable of recovering or replacing damaged cardiac muscle require physiologically relevant environments to provide the appropriate mechanical cues. The goal of this work is to better understand the subcellular responses of immature cardiomyocytes using an in vitro cardiac cell culture model that realistically mimics in vivo mechanical conditions, including cyclical fluid flows, chamber pressures, and tissue strains that could be experienced by implanted cardiac tissues. Cardiomyocytes were cultured in a novel microfluidic cardiac cell culture model (CCCM) to achieve accurate replication of the mechanical cues experienced by ventricular CM. Day 10 chick embryonic ventricular CM (3.5 × 104 cell clusters per cell chamber) were cultured for 4 days in the CCCM under cyclic mechanical stimulation (10 mmHg, 8–15% stretch, 2 Hz frequency) and ventricular cells from the same embryo were cultured in a static condition for 4 days as controls. Additionally, ventricular cell suspensions and ventricular tissue from day 16 chick embryo were collected and analyzed for comparison with CCCM cultured CM. The gene expressions and protein synthesis of calcium handling proteins decreased significantly during the isolation process. Mechanical stimulation of the cultured CM using the CCCM resulted in an augmentation of gene expression and protein synthesis of calcium handling proteins compared to the 2D constructs cultured in the static conditions. Further, the CCCM conditioned 2D constructs have a higher beat rate and contractility response to isoproterenol. These results demonstrate that early mechanical stimulation of embryonic cardiac tissue is necessary for tissue proliferation and for protein synthesis of the calcium handling constituents required for tissue contractility. Thus, physiologic mechanical conditioning may be essential for generating functional cardiac patches for replacement of injured cardiac tissue.