Casein Kinase 1 Phosphomimetic Mutations Negatively Impact Connexin-43 Gap Junctions in Human Pluripotent Stem Cell-Derived Cardiomyocytes.

connexin 43 gap junctions human pluripotent stem cell-derived cardiomyocytes phosphorylation

Journal

Biomolecules
ISSN: 2218-273X
Titre abrégé: Biomolecules
Pays: Switzerland
ID NLM: 101596414

Informations de publication

Date de publication:
02 Jan 2024
Historique:
received: 10 11 2023
revised: 14 12 2023
accepted: 25 12 2023
medline: 23 1 2024
pubmed: 23 1 2024
entrez: 23 1 2024
Statut: epublish

Résumé

The transplantation of human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) has shown promise in preclinical models of myocardial infarction, but graft myocardium exhibits incomplete host-graft electromechanical integration and a propensity for pro-arrhythmic behavior. Perhaps contributing to this situation, hPSC-CM grafts show low expression of connexin 43 (Cx43), the major gap junction (GJ) protein, in ventricular myocardia. We hypothesized that Cx43 expression and function could be rescued by engineering Cx43 in hPSC-CMs with a series of phosphatase-resistant mutations at three casein kinase 1 phosphorylation sites (Cx43-S3E) that have been previously reported to stabilize Cx43 GJs and reduce arrhythmias in transgenic mice. However, contrary to our predictions, transgenic Cx43-S3E hPSC-CMs exhibited reduced Cx43 expression relative to wild-type cells, both at baseline and following ischemic challenge. Cx43-S3E hPSC-CMs showed correspondingly slower conduction velocities, increased automaticity, and differential expression of other connexin isoforms and various genes involved in cardiac excitation-contraction coupling. Cx43-S3E hPSC-CMs also had phosphorylation marks associated with Cx43 GJ internalization, a finding that may account for their impaired GJ localization. Taken collectively, our data indicate that the Cx43-S3E mutation behaves differently in hPSC-CMs than in adult mouse ventricular myocytes and that multiple biological factors likely need to be addressed synchronously to ensure proper Cx43 expression, localization, and function.

Identifiants

pubmed: 38254663
pii: biom14010061
doi: 10.3390/biom14010061
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Canada Research Chairs Program
ID : CRC-2020-00245
Organisme : University of Toronto's Medicine by Design/Canada First Research Excellence Fund initiative, the Government of Canada's New Frontiers in Research Fund
ID : NFRF-2022-00447
Organisme : U.S. National Institutes of Health grant number
ID : GM55632
Organisme : BlueRock Therapeutics
ID : Sponsored research agreement

Auteurs

Rasha Al-Attar (R)

McEwen Stem Cell Institute, University Health Network, Toronto, ON M5G 1L7, Canada.

Joseph Jargstorf (J)

McEwen Stem Cell Institute, University Health Network, Toronto, ON M5G 1L7, Canada.

Rocco Romagnuolo (R)

McEwen Stem Cell Institute, University Health Network, Toronto, ON M5G 1L7, Canada.

Mariam Jouni (M)

McEwen Stem Cell Institute, University Health Network, Toronto, ON M5G 1L7, Canada.

Faisal J Alibhai (FJ)

McEwen Stem Cell Institute, University Health Network, Toronto, ON M5G 1L7, Canada.

Paul D Lampe (PD)

Translational Research Program, Public Health Sciences and Human Biology Divisions, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.

Joell L Solan (JL)

Translational Research Program, Public Health Sciences and Human Biology Divisions, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.

Michael A Laflamme (MA)

McEwen Stem Cell Institute, University Health Network, Toronto, ON M5G 1L7, Canada.
Peter Munk Cardiac Centre, University Health Network, Toronto, ON M5G 1L7, Canada.
Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON M5G 1L7, Canada.

Classifications MeSH