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Title: | Systems for the Functional Evaluation of Human Heart Tissues Derived from Pluripotent Stem Cells |
Authors: | Murata, Kozue Masumoto, Hidetoshi |
Author's alias: | 村田, 梢 升本, 英利 |
Keywords: | organ-on-a-chip pluripotent stem cell cardiomyocyte cardiotoxicity |
Issue Date: | Jun-2022 |
Publisher: | Oxford University Press (OUP) |
Journal title: | Stem Cells |
Volume: | 40 |
Issue: | 6 |
Start page: | 537 |
End page: | 545 |
Abstract: | Human pluripotent stem cells (hPSCs) are expected to be a promising cell source in regenerative medicine and drug discovery for the treatment of various intractable diseases. An approach for creating a 3-dimensional (3D) structure from hPSCs that mimics human cardiac tissue functions has made it theoretically possible to conduct drug discovery and cardiotoxicity tests by assessing pharmacological responses in human cardiac tissues by a screening system using a compound library. The myocardium functions as a tissue composed of organized vascular networks, supporting stromal cells and cardiac muscle cells. Considering this, the reconstruction of tissue structure by various cells of cardiovascular lineages, such as vascular cells and cardiac muscle cells, is desirable for the ideal conformation of hPSC-derived cardiac tissues. Heart-on-a-chip, an organ-on-a-chip system to evaluate the physiological pump function of 3D cardiac tissues might hold promise in medical researchs such as drug discovery and regenerative medicine. Here, we review various modalities to evaluate the function of human stem cell-derived cardiac tissues and introduce heart-on-a-chip systems that can recapitulate physiological parameters of hPSC-derived cardiac tissues. |
Rights: | © The Author(s) 2022. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
URI: | http://hdl.handle.net/2433/279357 |
DOI(Published Version): | 10.1093/stmcls/sxac022 |
PubMed ID: | 35303744 |
Appears in Collections: | Journal Articles |
This item is licensed under a Creative Commons License