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  3. Promoting differentiation of human-induced pluripotent stem cells into sinoatrial node-like cells through programmed regulation of AMPK signalling pathway

Promoting differentiation of human-induced pluripotent stem cells into sinoatrial node-like cells through programmed regulation of AMPK signalling pathway

  • Europace. 2025 Oct 31;27(11):euaf288. doi: 10.1093/europace/euaf288.
Feng Liu 1 2 3 4,  Zongqian Xue 1 5,  Huan Lan 3,  Juyi Wan 2 3,  Chenyu Yang 1 4,  Lukas Cyganek 6 7,  Nazha Hamdani 8 9 10,  Fengxu Yu 2 3,  Bin Liao 2 3,  Xiaobo Zhou 1 2 3 4,  Ibrahim El-Battrawy 8 9 10,  Ibrahim Akin 1 4
Affiliations

Affiliations

  • 1 Department of Cardiology, Angiology, Hemostaseology and Medical Intensive Care, Medical Faculty Mannheim, University Medical Centre Mannheim (UMM), Heidelberg University, Theodor-Kutzer-Ufer 1-3, Mannheim 68167, Germany.
  • 2 Department of Cardiovascular Surgery, the Affiliated Hospital, Metabolic Vascular Diseases Key Laboratory of Sichuan Province, Key Laboratory of Cardiovascular Remodelling and Dysfunction, Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
  • 3 Key Laboratory of Medical Electrophysiology of Ministry of Education & Medical Electrophysiological Key Laboratory of Sichuan Province, Collaborative Innovation Center for Prevention of Cardiovascular Diseases, Institute of Cardiovascular Research, Southwest Medical University, Luzhou, Sichuan 646000, P.R. China.
  • 4 German Center for Cardiovascular Research (DZHK), Partner Site Heidelberg/Mannheim, Mannheim, Germany.
  • 5 Department of Cardiology, Aoyang Hospital Affiliated to Jiangsu University, Zhangjiagang, Jiangsu 215600, P.R. China.
  • 6 Stem Cell Unit, Clinic for Cardiology and Pneumology, University Medical Center Göttingen, Göttingen, Germany.
  • 7 DZHK (German Center for Cardiovascular Research), Partner Site Göttingen, Göttingen, Germany.
  • 8 Institute of Physiology, Department of Cellular and Translational Physiology, Medical Faculty, Ruhr University Bochum, Bochum, Germany.
  • 9 Institut für Forschung und Lehre (IFL), Molecular and Experimental Cardiology, Ruhr University Bochum, Bochum, Germany.
  • 10 Department of Cardiology and Rhythmology, St. Josef Hospital, Ruhr University Bochum, Bochum, Germany.
PMID: 41206581 DOI: 10.1093/europace/euaf288
Abstract

Aims: The differentiation of human-induced pluripotent stem cells (hiPSCs) into sinoatrial node (SAN)-like cells (SANLCs) remains challenged by complex differentiation protocols and low efficiency. This study aims to reveal the role of AMPK signalling in the differentiation process of hiPSCs into SANLCs, providing new strategies for obtaining SANLCs in vitro.

Methods and results: Cells from the cardiac mesodermal stage, cardiac progenitor cell stage, and cardiomyocyte stage during differentiation of hiPSCs to cardiomyocytes (hiPSC-CMs) were taken for transcriptome Sequencing and analyses. PCR, immunostaining, western blot, FACS, and patch-clamp techniques were employed for the analyses of differentiated hiPSC-CMs. Kyoto Encyclopedia of Genes and Genomes analysis identified that the AMPK signalling pathway is significantly enriched with the expression of NKX2.5 (sinus node cell development-related transcription factor). The early activation and late inhibition of AMPK signalling were both effective in the up-regulation of SANLC markers. In addition, the combined manipulation of both stages further enhanced the differentiation efficiency reflected by higher SANLC marker expression, which was also confirmed at the protein level by immunofluorescence, western blot, and flow cytometry analyses. SANLCs obtained from the differentiation with combined modulation of AMPK signalling displayed typical features of native pacemaker cells in the heart, including ion channel currents (IKAch, ICaT, ICaL, If), action potentials, and robust autonomic responsiveness to both β-adrenergic and muscarinic stimulation.

Conclusion: Early activation and then inhibition of the AMPK signalling pathway during the differentiation process can promote hiPSC differentiation to SANLCs, which may provide a novel strategy for obtaining SANLCs for studies on SAN diseases.

Keywords

AMPK signalling; Human-induced pluripotent stem cells; Sinoatrial node-like cells.

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