State-of-the-Art Differentiation Protocols for Patient-Derived Cardiac Pacemaker Cells.

hiPSC-derived cardiac pacemaker cells protocols sinoatrial node

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
16 Mar 2024
Historique:
received: 15 02 2024
revised: 12 03 2024
accepted: 14 03 2024
medline: 28 3 2024
pubmed: 28 3 2024
entrez: 28 3 2024
Statut: epublish

Résumé

Human-induced pluripotent stem cell (hiPSC)-derived cardiomyocytes raise the possibility of generating pluripotent stem cells from a wide range of human diseases. In the cardiology field, hiPSCs have been used to address the mechanistic bases of primary arrhythmias and in investigations of drug safety. These studies have been focused primarily on atrial and ventricular pathologies. Consequently, many hiPSC-based cardiac differentiation protocols have been developed to differentiate between atrial- or ventricular-like cardiomyocytes. Few protocols have successfully proposed ways to obtain hiPSC-derived cardiac pacemaker cells, despite the very limited availability of human tissues from the sinoatrial node. Providing an in vitro source of pacemaker-like cells would be of paramount importance in terms of furthering our understanding of the mechanisms underlying sinoatrial node pathophysiology and testing innovative clinical strategies against sinoatrial node dysfunction (i.e., biological pacemakers and genetic- and pharmacological- based therapy). Here, we summarize and detail the currently available protocols used to obtain patient-derived pacemaker-like cells.

Identifiants

pubmed: 38542361
pii: ijms25063387
doi: 10.3390/ijms25063387
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Fondation Leducq
ID : TNE 19CV03
Organisme : Agence Nationale de la Recherche
ID : ANR-22-CE17-0012-02

Auteurs

Eleonora Torre (E)

Institut de Génomique Fonctionnelle, Université de Montpellier, CNRS, INSERM, 34090 Montpellier, France.
LabEx Ion Channels Science and Therapeutics (ICST), 06560 Valbonne, France.

Matteo E Mangoni (ME)

Institut de Génomique Fonctionnelle, Université de Montpellier, CNRS, INSERM, 34090 Montpellier, France.
LabEx Ion Channels Science and Therapeutics (ICST), 06560 Valbonne, France.

Alain Lacampagne (A)

PhyMedExp, University of Montpellier, Inserm, CNRS, 371 Avenue du Doyen G. Giraud, CEDEX 5, 34295 Montpellier, France.

Albano C Meli (AC)

PhyMedExp, University of Montpellier, Inserm, CNRS, 371 Avenue du Doyen G. Giraud, CEDEX 5, 34295 Montpellier, France.
Montpellier Organoid Platform, Biocampus, University of Montpellier, CNRS, INSERM, 34090 Montpellier, France.

Pietro Mesirca (P)

Institut de Génomique Fonctionnelle, Université de Montpellier, CNRS, INSERM, 34090 Montpellier, France.
LabEx Ion Channels Science and Therapeutics (ICST), 06560 Valbonne, France.

Classifications MeSH