A novel method of cultivating cardiac myocytes in agarose microchamber chips for studying cell synchronization
© Kojima et al; licensee BioMed Central Ltd. 2004
Received: 20 December 2003
Accepted: 09 September 2004
Published: 09 September 2004
We have developed a new method that enables agar microstructures to be used to cultivate cardiac myocyte cells in a manner that allows their connection patterns to be controlled. Non-contact three-dimensional photo-thermal etching with a 1064-nm infrared focused laser beam was used to form the shapes of agar microstructures. This wavelength was selected as it is not absorbed by water or agar. Identical rat cardiac myocytes were cultured in adjacent microstructures connected by microchannels and the interactions of asynchronous beating cardiac myocyte cells observed. Two isolated and independently beating cardiac myocytes were shown to form contacts through the narrow microchannels and by 90 minutes had synchronized their oscillations. This occurred by one of the two cells stopping their oscillation and following the pattern of the other cell. In contrast, when two sets of synchronized beating cells came into contact, those two sets synchronized without any observable interruptions to their rhythms. The results indicate that the synchronization process of cardiac myocytes may be dependent on the community size and network pattern of these cells.
Single-cell based analysis methods have become more and more important for understanding the cell-group effects such as how information is controlled and recorded in a cell group or a network shape. Early tissue culture studies of cardiac myocyte cells demonstrated that a single beating cell can influence the rate of a neighbouring cell in close contact and that a group of heart cells in a culture, beating synchronously with a rapid rhythm, can act as pacemaker for a contiguous cell sheet . Though the former results predicted that a rapidly beating region of tissue acts as pacemaker for a slower one and examined how the synchronization process of two isolated beating cardiac myocytes , the cell-to-cell connection could not be controlled completely without using microstructures on the cultivation plate. As means of attaining the spatial arrangement of cardiac myocytes, we have developed a new single-cell cultivation method and a system using agar microstructures, based on 1064-nm photo-thermal etching [3–6]. We have also developed the on-chip single-cell sorting method for cultivating particular cells chosen from clued mixture of cells , and have found the adaptation process of epigenetic memorization in cells by storing the information as the localization of proteins .
This paper reports the practical use of the agar chamber for screening the community size effect of the synchronization process of adjacent cardiac myocyte cells having independent oscillation.
Neonatal rat cardiac myocytes were isolated and purified as follows. First, the hearts of 1- to 3-day-old Wistar rats (Nippon Bio-supp. Center, Tokyo, Japan) were excised under ether anaesthesia. The ventricles were separated from the atria and then washed with phosphate buffered saline (PBS, 137 mM NaCl, 2.7 mM KCl, 8 mM Na2 HPO4, 1.5 mM KH2PO4, pH 7.4) containing 0.9 mM CaCl2 and 0.5 mM MgCl2. The ventricles were minced in PBS without CaCl2 or MgCl2 and then incubated in PBS containing 0.25% collagenase (Wako, Osaka, Japan) for 30 minutes at 37°C to digest the ventricular tissue. This procedure was repeated twice more and the cell suspension was then transferred to cell culture medium (DMEM [Invitrogen Corp., Carlsbad, CA USA] supplemented with 10% fetal bovine serum, 100 U/ml penicillin, and 100 μg/ml Streptomycin) at 4°C. The cells were filtered through a 40-μm nylon mesh and centrifuged at 180 g for 5 minutes at room temperature. The cell pellet was re-suspended in a HEPES buffer (20 mM HEPES, 110 mM NaCl, 1 mM NaH2PO4, 5 mM glucose, 5 mM KCl, and 1 mM MgSO4, pH 7.4). Cardiac myocytes present in the suspension were separated from other cells (i.e., fibroblasts and endothelial cells) by the density centrifugation method. The cell suspension was then layered onto 40.5% Percoll (Amersham Biosciences, Uppsala, Sweden) diluted in the HEPES buffer, which had previously been layered onto 58.5% Percoll diluted in the same buffer. The cell suspension was then centrifuged at 2200 g for 30 minutes at room temperature. Cardiac myocytes were retrieved from the interface of the 40.5% and 58.5% Percoll layers. Retrieved cells were then re-suspended in the cell culture medium. An aliquot (5- μl) of the suspension was diluted to achieve a final concentration of 3.0 × 105 cells/ml then plated into the chip. Individual cardiac myocytes were picked up by a micropipette and manually introduced into each chip microchamber and incubated on a cell-cultivation microscope system at 37°C in the presence of a humidified atmosphere of 95% air /5% CO2. It should be noted that because the microchamber sidewalls were made of agar, then the cells could not easily pass over the chambers.
Phase-contrast microscopy was used to measure the contraction rhythm of the cardiac myocytes and the network formation of cells in the two adjacent chambers that were connected by the focused beam.
The spontaneous contraction rhythm of cultured cardiac myocytes was evaluated by a video-image recording method. Images of beating cardiac myocytes were recorded with a CCD camera through the use of a phase contrast microscope. The sizes (cross-section of volume) of cardiac myocytes, which changed considerably with contraction, were also analyzed and recorded every 1/30 s by a personal computer with a video capture board.
Additional File 1: two cells. synchronized oscillation of the two cells (MPG 5 MB)
The same method was also used to make more complicated network patterns of cardiac myocytes. Figure 1 shows a micrograph of a four-cell network. As shown in the graph (Fig. 1), two sets of the beating pairs synchronized without having to stop unlike that previously observed for the synchronization of isolated cells (see additional file 2 "movie2.mpg"). This suggests that the synchronization dynamics and rhythm of the cell group is more stable than that of single cells.
In conclusion, we present a 1064-nm photo-thermal etching technology with which to create agarose microchambers for growing networks of cardiac myocyte cells. Using the system, we first observed the differences of the synchronization process of cardiac myocyte cells and their dependence on community size. This system has great potential for use in the biological/medical fields for cultivating the next stage of single-cell based networks and measuring their properties in laboratories.
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