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iPSC-Derived Endothelial Cells as Experimental Models for Predictive and Personalized Strategies in Cardiovascular
Lorenzo Fontanelli1, Alessio Castronovo1, Carolina Ferri2
1Health Science Interdisciplinary Centre, Sant'Anna School of Advanced Studies, 56124 Pisa, Italy.
Insights
Patient-specific human-induced pluripotent stem cell-derived endothelial cells (hiPSC-ECs) offer personalized models for studying vascular diseases. These models help understand disease mechanisms and guide targeted therapy development.
Area of Science:
- Cardiovascular Research
- Stem Cell Biology
- Vascular Biology
Background:
- Endothelial cells (ECs) are crucial for vascular homeostasis.
- EC dysfunction contributes significantly to cardiovascular and cerebrovascular diseases.
Purpose of the Study:
- To review the application of patient-specific hiPSC-ECs in personalized medicine.
- To explore their use in modeling endothelial dysfunction and disease pathology.
- To discuss limitations and future directions for hiPSC-EC-based research.
Main Methods:
- Utilizing human-induced pluripotent stem cells (hiPSCs) to generate patient-specific endothelial cells (hiPSC-ECs).
- Directing hiPSC-ECs toward specific vascular phenotypes (arterial, venous, organotypic).
- Developing and employing 2D and 3D in vitro models for disease simulation.
Main Results:
- hiPSC-ECs enable personalized in vitro modeling of endothelial pathology.
- These models facilitate the dissection of disease mechanisms.
- Patient-specific hiPSC-ECs aid in prioritizing targeted therapies.
Conclusions:
- hiPSC-ECs represent a powerful tool for personalized cardiovascular research.
- Further integration of hiPSC-EC assays into treatment algorithms is promising.
- Addressing current limitations will enhance the clinical utility of hiPSC-EC models.
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.
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