Evidence map›Paper›PMID 33015053›Full record

ArticleFrontiers in cell and developmental biology2020

Optimizing the Direction and Order of the Motion Unveiled the Ability of Conventional Monolayers of Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes to Show Frequency-Dependent Enhancement of Contraction and Relaxation Motion.

Hiroko Izumi-Nakaseko, Koki Chiba, Mihoko Hagiwara-Nagasawa, Ayano Satsuka, Ai Goto, Yoshio Nunoi, Ryuichi Kambayashi, Akio Matsumoto, Yoshinori Takei, Yasunari Kanda and 2 more

Abstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Hiroko Izumi-NakasekoDepartment of Pharmacology, Faculty of Medicine, Toho University, Tokyo, Japan.
Koki ChibaDepartment of Pharmacology, Faculty of Medicine, Toho University, Tokyo, Japan.
Mihoko Hagiwara-NagasawaDepartment of Pharmacology, Faculty of Medicine, Toho University, Tokyo, Japan.
Ayano SatsukaDivision of Pharmacology, National Institute of Health Sciences, Kanagawa, Japan.
Ai GotoDepartment of Pharmacology, Faculty of Medicine, Toho University, Tokyo, Japan.
Yoshio NunoiDepartment of Pharmacology, Faculty of Medicine, Toho University, Tokyo, Japan.
Ryuichi KambayashiDepartment of Pharmacology, Faculty of Medicine, Toho University, Tokyo, Japan.
Akio MatsumotoDepartment of Aging Pharmacology, Faculty of Medicine, Toho University, Tokyo, Japan.
Yoshinori TakeiDepartment of Translational Research & Cellular Therapeutics, Faculty of Medicine, Toho University, Tokyo, Japan.
Yasunari KandaDivision of Pharmacology, National Institute of Health Sciences, Kanagawa, Japan.
Atsuhiko T NaitoDepartment of Physiology, Division of Cell Physiology, Graduate School of Medicine, Toho University, Tokyo, Japan.
Atsushi SugiyamaDepartment of Pharmacology, Faculty of Medicine, Toho University, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Contractility of the human heart increases as its beating rate is elevated, so-called positive force-frequency relationship; however, human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) have been reported to exert a negative force-frequency relationship. We tested the hypothesis that the regulation of motion directions by electrical pacing and/or oxygen supply may improve the electro-mechanical properties of hiPSC-CMs monolayers. To better evaluate the spatial and temporal relationship between electrical excitation and contractile motion, we simultaneously observed the field potential and motion vector of hiPSC-CMs sheets. Under spontaneous contraction, although an electrical excitation originating from a region propagated unidirectionally over the cell sheet, contraction wave started from multiple sites, and relaxation wave was initiated from a geometric center of hiPSC-CMs sheet. During electrical pacing, contraction and relaxation waves were propagated from the stimulated site. Interestingly, the maximum contraction speed was more increased when the hiPSC-CMs sheet was stimulated at an area relaxation initiated under spontaneous condition. Furthermore, motion vector analysis demonstrated that "positive contraction velocity-frequency relationship" in contraction and "frequency-dependent enhancement of relaxation" were produced in the cell sheet by optimizing the direction and order of the contractile motion with pacing at the relaxation-initiating area. A close analysis of motion vectors along with field potential recording demonstrated that relaxation process consists of fast and slow phases, and suggest that intracellular Ca

Indexed as

contraction velocity-frequency relationshipfield potentialfrequency-dependent enhancement of relaxationhuman induced pluripotent stem cell-derived cardiomyocytesmotion vector

Identifiers

PMID33015053
PMCPMC7511828

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