Geometric understanding of local fluctuation distribution of conduction time in lined-up cardiomyocyte network in agarose-microfabrication multi-electrode measurement assay

Kazufumi Sakamoto, Shota Aoki, Yuhei Tanaka, Kenji Shimoda, Yoshitsune Hondo, Kenji Yasuda*

*この研究の対応する著者

研究成果: Article査読

2 被引用数 (Scopus)

抄録

We examined characteristics of the propagation of conduction in width-controlled cardiomyocyte cell networks for understanding the contribution of the geometrical arrangement of cardiomyocytes for their local fluctuation distribution. We tracked a series of extracellular field potentials of linearly lined-up human embryonic stem (ES) cell-derived cardiomyocytes and mouse primary cardiomyocytes with 100 kHz sampling intervals of multi-electrodes signal acquisitions and an agarose microfabrication technology to localize the cardiomyocyte geometries in the lined-up cell networks with 100–300 µm wide agarose microstructures. Conduction time between two neighbor microelectrodes (300 µm) showed Gaussian distribution. However, the distributions maintained their form regardless of its propagation distances up to 1.5 mm, meaning propagation diffusion did not occur. In contrast, when Quinidine was applied, the propagation time distributions were increased as the faster firing regulation simulation predicted. The results indicate the “faster firing regulation” is not sufficient to explain the conservation of the propagation time distribution in cardiomyocyte networks but should be expanded with a kind of community effect of cell networks, such as the lower fluctuation regulation.

本文言語English
論文番号1105
ページ(範囲)1-14
ページ数14
ジャーナルMicromachines
11
12
DOI
出版ステータスPublished - 2020 12月

ASJC Scopus subject areas

  • 制御およびシステム工学
  • 機械工学
  • 電子工学および電気工学

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