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培养过程中愿原力不与你同在:消除培养过程中机械相关反馈可保留培养的心房细胞和起搏细胞功能。

May the Force Not Be With You During Culture: Eliminating Mechano-Associated Feedback During Culture Preserves Cultured Atrial and Pacemaker Cell Functions.

作者信息

Kirschner Peretz Noa, Segal Sofia, Yaniv Yael

机构信息

Biomedical Engineering Faculty, Technion Israel Institute of Technology, Haifa, Israel.

出版信息

Front Physiol. 2020 Mar 20;11:163. doi: 10.3389/fphys.2020.00163. eCollection 2020.

Abstract

Cultured cardiomyocytes have been shown to possess significant potential as a model for characterization of mechano-Ca, mechano-electric, and mechano-metabolic feedbacks in the heart. However, the majority of cultured cardiomyocytes exhibit impaired electrical, mechanical, biochemical, and metabolic functions. More specifically, the cells do not beat spontaneously (pacemaker cells) or beat at a rate far lower than their physiological counterparts and self-oscillate (atrial and ventricular cells) in culture. Thus, efforts are being invested in ensuring that cultured cardiomyocytes maintain the shape and function of freshly isolated cells. Elimination of contraction during culture has been shown to preserve the mechano-Ca, mechano-electric, and mechano-metabolic feedback loops of cultured cells. This review focuses on pacemaker cells, which reside in the sinoatrial node (SAN) and generate regular heartbeat through the initiation of the heart's electrical, metabolic, and biochemical activities. In parallel, it places emphasis on atrial cells, which are responsible for bridging the electrical conductance from the SAN to the ventricle. The review provides a summary of the main mechanisms responsible for mechano-electrical, Ca, and metabolic feedback in pacemaker and atrial cells and of culture methods existing for both cell types. The work concludes with an explanation of how the elimination of mechano-electrical, mechano-Ca, and mechano-metabolic feedbacks during culture results in sustained cultured cell function.

摘要

培养的心肌细胞已被证明具有巨大潜力,可作为表征心脏机械-钙、机械-电和机械-代谢反馈的模型。然而,大多数培养的心肌细胞表现出电、机械、生化和代谢功能受损。更具体地说,这些细胞在培养中不会自发搏动(起搏细胞),或者搏动频率远低于其生理对应物,也不会自我振荡(心房和心室细胞)。因此,人们正在努力确保培养的心肌细胞保持新鲜分离细胞的形态和功能。已证明在培养过程中消除收缩可保留培养细胞的机械-钙、机械-电和机械-代谢反馈回路。本综述重点关注位于窦房结(SAN)的起搏细胞,它们通过启动心脏的电、代谢和生化活动来产生规律的心跳。同时,它还强调了心房细胞,它们负责将电传导从窦房结桥接到心室。该综述总结了起搏细胞和心房细胞中机械-电、钙和代谢反馈的主要机制以及这两种细胞类型现有的培养方法。文章最后解释了在培养过程中消除机械-电、机械-钙和机械-代谢反馈如何导致培养细胞功能的持续。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99e2/7100534/07ca95a8ce9f/fphys-11-00163-g001.jpg

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