Human-induced pluripotent stem cell-derived cardiomyocytes, 3D cardiac structures, and heart-on-a-chip as tools for drug research

K Andrysiak, J Stępniewski, J Dulak - Pflügers Archiv-European Journal of …, 2021 - Springer
Abstract Development of new drugs is of high interest for the field of cardiac and
cardiovascular diseases, which are a dominant cause of death worldwide. Before being …

RYR2-ryanodinopathies: from calcium overload to calcium deficiency

C Steinberg, TM Roston, C van der Werf, S Sanatani… - Europace, 2023 - academic.oup.com
The sarcoplasmatic reticulum (SR) cardiac ryanodine receptor/calcium release channel
RyR2 is an essential regulator of cardiac excitation–contraction coupling and intracellular …

Personalized medicine in the dish to prevent calcium leak associated with short-coupled polymorphic ventricular tachycardia in patient-derived cardiomyocytes

Y Sleiman, S Reiken, A Charrabi, F Jaffré… - Stem Cell Research & …, 2023 - Springer
Background Polymorphic ventricular tachycardia (PMVT) is a rare genetic disease
associated with structurally normal hearts which in 8% of cases can lead to sudden cardiac …

Decoding genetics of congenital heart disease using patient-derived induced pluripotent stem cells (iPSCs)

H Lin, KL McBride, V Garg, MT Zhao - Frontiers in Cell and …, 2021 - frontiersin.org
Congenital heart disease (CHD) is the most common cause of infant death associated with
birth defects. Recent next-generation genome sequencing has uncovered novel genetic …

“Ryanopathies” and RyR2 dysfunctions: can we further decipher them using in vitro human disease models?

Y Sleiman, A Lacampagne, AC Meli - Cell Death & Disease, 2021 - nature.com
The regulation of intracellular calcium (Ca2+) homeostasis is fundamental to maintain
normal functions in many cell types. The ryanodine receptor (RyR), the largest intracellular …

[HTML][HTML] Patient-specific induced pluripotent stem cells as “disease-in-a-dish” models for inherited cardiomyopathies and channelopathies–15 years of research

MM Micheu, AM Rosca - World journal of stem cells, 2021 - ncbi.nlm.nih.gov
Among inherited cardiac conditions, a special place is kept by cardiomyopathies (CMPs)
and channelopathies (CNPs), which pose a substantial healthcare burden due to the …

Impact of neurons on patient-derived cardiomyocytes using organ-on-A-chip and iPSC biotechnologies

AA Bernardin, S Colombani, A Rousselot, V Andry… - Cells, 2022 - mdpi.com
In the heart, cardiac function is regulated by the autonomic nervous system (ANS) that
extends through the myocardium and establishes junctions at the sinus node and ventricular …

Using hiPSC‐CMs to examine mechanisms of catecholaminergic polymorphic ventricular tachycardia

A Arslanova, S Shafaattalab, K Ye, P Asghari… - Current …, 2021 - Wiley Online Library
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a potentially lethal
inherited cardiac arrhythmia condition, triggered by physical or acute emotional stress, that …

A SPRY1 domain cardiac ryanodine receptor variant associated with short-coupled torsade de pointes

Z Touat-Hamici, M Blancard, R Ma, L Lin, Y Iddir… - Scientific Reports, 2021 - nature.com
Idiopathic ventricular fibrillation (IVF) causes sudden death in young adult patients without
structural or ischemic heart disease. Most IVF cases are sporadic and some patients present …

[HTML][HTML] Progress of organoid platform in cardiovascular research

X Du, H Jia, Y Chang, Y Zhao, J Song - Bioactive Materials, 2024 - Elsevier
Cardiovascular disease is a significant cause of death in humans. Various models are
necessary for the study of cardiovascular diseases, but once cellular and animal models …