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.

Figure Figure11 shows the schematic drawing of the agar microchambers on the chip. The microchambers and microchannels were constructed by localized melting of a portion of the 5-μm-thick agar layer using a 1064-nm the infrared focused laser beam, a process we have termed photo-thermal etching. The 1064-nm laser beam is not absorbed by either water or the agar, and selectively melts a portion of the agar just near the chromium thin layer as this layer absorbs the beam energy. Microstructures such as holes and channels can be easily produced using this non-contact etching within only a few minutes without the requirement of any cast moulding process. The melting of agar by laser occurred as follows: (a) the 1064-nm infrared laser beam was focused on the agar layer on the glass slide; (b) the agar at the focal point and on the light pathway started to melt; (c) when the focused beam was moved parallel to the chip surface, a portion of agar around the focal spot of laser melted and diffused into water; (d) after the heated spot had been moved, a channel was created at the bottom of the agar layer connecting the two adjacent holes. The microscope confirmed the melting had occurred, and then either the heating was continued until the spot size reached the desired size, or the heating position was shifted to achieve the desired shape. Cardiac myocytes were cultivated in each hole of the agar microchambers on the chip as shown in Fig. Fig.1.1. Collagen-type I (Nitta gelatin, Osaka, Japan) was coated on the glass layer surface to improve the attachment of the cell to the bottom of the microchambers.

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.

Figure Figure11 shows a micrograph image of two isolated, independently beating cardiac myocytes coming into contact through the microchannel. Ninety min after the physical contact, the two connected cells started to oscillate synchronously. The time course change of the heart beating was as shown in Fig. Fig.1.1. As shown in the graph, the process of synchronization was accomplished only after one of the cells stopped beating and then synchronized its oscillation with other cell. Movie 1 (see additional file 1 "movie1.mpg") depicts the process of beating synchronization. Once the synchronized oscillation of the two cells was accomplished (arrowhead in Fig. Fig.1),1), then the two cells maintained synchronization similar to that observed in whole tissue. A time interval of approximately 90 min was needed to form the gap junction between the two adjacent cells.

The same method was also used to make more complicated network patterns of cardiac myocytes. Figure Figure11 shows a micrograph of a four-cell network. As shown in the graph (Fig. (Fig.1),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.