iPSC-Derived Endothelial Cells as Experimental Models for Predictive and Personalized Strategies in Cardiovascular and Cerebrovascular Disease

Endothelial cells (ECs) regulate vascular homeostasis, and their dysfunction is a key driver of many cardiovascular and cerebrovascular diseases. Human-induced pluripotent stem cell-derived endothelial cells (hiPSC-ECs) provide access to patient-specific vascular cells that can be directed toward arterial, venous, or organotypic phenotypes, enabling personalized in vitro modeling of endothelial pathology. In this review, we discuss how patient-specific iPSC-ECs are used as predictive and personalized two- and three-dimensional models to dissect disease mechanisms and prioritize targeted therapies. We highlight some limitations of this methodology and outline future directions for integrating iPSC-EC-based assays into individualized treatment algorithms.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2026-01-13
DOI
https://doi.org/10.3390/ijms27020780
Citations
1
Primary Topic
Angiogenesis and VEGF in Cancer
Type
article
Field-Weighted Citation Impact
22.24
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article

iPSC-Derived Endothelial Cells as Experimental Models for Predictive and Personalized Strategies in Cardiovascular and Cerebrovascular Disease

F RECCHIA, Andrea Borghini, Lorenzo Fontanelli, Federico Vozzi et al.
1 citations
International Journal of Molecular Sciences
Angiogenesis and VEGF in Cancer
22.24
article

iPSC-Derived Endothelial Cells as Experimental Models for Predictive and Personalized Strategies in Cardiovascular and Cerebrovascular Disease

F RECCHIA, Andrea Borghini, Lorenzo Fontanelli, Federico Vozzi, Alessio Castronovo, Carolina Ferri
article en
1 citations

Abstract

Endothelial cells (ECs) regulate vascular homeostasis, and their dysfunction is a key driver of many cardiovascular and cerebrovascular diseases. Human-induced pluripotent stem cell-derived endothelial cells (hiPSC-ECs) provide access to patient-specific vascular cells that can be directed toward arterial, venous, or organotypic phenotypes, enabling personalized in vitro modeling of endothelial pathology. In this review, we discuss how patient-specific iPSC-ECs are used as predictive and personalized two- and three-dimensional models to dissect disease mechanisms and prioritize targeted therapies. We highlight some limitations of this methodology and outline future directions for integrating iPSC-EC-based assays into individualized treatment algorithms.

International Journal of Molecular SciencesVol. 27(2)
University of Pisa (IT), Scuola Superiore Sant'Anna (IT), University of Chicago (US), Istituto di Fisiologia Clinica (IT)
Good health and well-being
Openalex Percentile: Top 3%
Angiogenesis and VEGF in Cancer
22.24
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