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New Modalities of 3D Pluripotent Stem Cell-Based Assays in Cardiovascular Toxicity
Orsolits, B. [Orsolits, Barbara (Idegi sejtbiológia), szerző] Kardiológia Központ - Kardiológiai Tanszék (SE / AOK / K)
;
Kovács, Z.
;
Kriston-Vizi, J.
;
Merkely, B. [Merkely, Béla Péter (Kardiológia), szerző] Kardiológia Központ - Kardiológiai Tanszék (SE / AOK / K); Sportorvostan Tanszék (SE / AOK / K)
;
Földes, G. ✉ [Földes, Gábor (Belgyógyászat, ka...), szerző] Kardiológia Központ - Kardiológiai Tanszék (SE / AOK / K)
Angol nyelvű Összefoglaló cikk (Folyóiratcikk) Tudományos
Megjelent:
FRONTIERS IN PHARMACOLOGY 1663-9812
12
Paper: 603016
, 10 p.
2021
SJR Scopus - Pharmacology (medical): Q1
Azonosítók
MTMT: 31980732
DOI:
10.3389/fphar.2021.603016
WoS:
000639131300001
Scopus:
85104018692
PubMed:
33854431
Támogatások:
(Higher Education Institutional Excellence Programme of the Ministry of Human Capacities in Hungary, within the framework of the Neurology thematic programme of the Semmelweis University)
National Heart Program(NVKP-16-1-2016-0017)
(128444)
The substantial progress of the human induced pluripotent stem cell (hiPSC) technologies over the last decade has provided us with new opportunities for cardiovascular drug discovery, regenerative medicine, and disease modeling. The combination of hiPSC with 3D culture techniques offers numerous advantages for generating and studying physiological and pathophysiological cardiac models. Cells grown in 3D can overcome many limitations of 2D cell cultures and animal models. Furthermore, it enables the investigation in an architecturally appropriate, complex cellular environment in vitro. Yet, generation and study of cardiac organoids—which may contain versatile cardiovascular cell types differentiated from hiPSC—remain a challenge. The large-scale and high-throughput applications require accurate and standardised models with highly automated processes in culturing, imaging and data collection. Besides the compound spatial structure of organoids, their biological processes also possess different temporal dynamics which require other methods and technologies to detect them. In this review, we summarise the possibilities and challenges of acquiring relevant information from 3D cardiovascular models. We focus on the opportunities during different time-scale processes in dynamic pharmacological experiments and discuss the putative steps toward one-size-fits-all assays. © Copyright © 2021 Orsolits, Kovács, Kriston-Vizi, Merkely and Földes.
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2025-03-30 06:05
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