Aug 2026· Cells· Vol 15· 0 citations· 209 references
Medicine
TL;DR
This review consolidates current progress and future potential of iPSC technology across five domains: technical reprogramming challenges and advances; conservation applications including genetic rescue, in vitro gametogenesis, and de-extinction; medical applications within a one medicine framework; agricultural applications spanning disease resistance, climate resilience, and cultured meat; and species-specific iPSC-derived systems in ecotoxicology.
Abstract
Induced pluripotent stem cells have revolutionized biomedical research—yet the vast majority of life on Earth remains beyond their reach. Non-model species lack the annotated genomes, validated reagents, and species-specific culture infrastructure that make iPSC technology routine in humans and mice, and this infrastructure deficit, compounded by genuine biological differences in pluripotency network architecture across taxa, is what has kept the field narrow. The deep conservation of the core pluripotency network across vertebrates suggests that reprogramming may, in principle, be achievable across a far broader range of species than currently demonstrated—though the extent to which this holds across more divergent taxa remains to be established. This review consolidates current progress and future potential of iPSC technology across five domains: technical reprogramming challenges and advances; conservation applications including genetic rescue, in vitro gametogenesis, and de-extinction; medical applications within a one medicine framework; agricultural applications spanning disease resistance, climate resilience, and cultured meat; and species-specific iPSC-derived systems in ecotoxicology. Throughout, we distinguish what has been demonstrated from what remains aspirational and identify the priorities that will determine whether the iPSC revolution can be extended—rigorously and at scale—beyond model organism research.
This Review evaluates the technological and translational trajectories that have defined the iPSC era and analyzes the operational barriers to therapeutic development, envisioning a paradigm shift in which iPSC-derived interventions transition from bespoke experimental models toward standardized, engineered biological...
Jaecheol Lee, Todd J. Herron, L. Studer et al.· Nature Medicine· 0 citations
This review summarizes the trajectory of iPSC reprogramming technologies and identifies the core “translational triltrilas”, namely, the inherent tradeoffs between security, homogeneity, and scalability, and proposes a comprehensive strategy to overcome these bottlenecks.
Meng-Meng Chen, N. Zuo, Qi Wang et al.· Frontiers in Cell and Develo...· 0 citations
The article traces the trend of directed differentiation technologies evolving from two-dimensional culture to three-dimensional organoids and details their practical applications in diseases such as stroke, Alzheimer's disease, and spinal cord injury—particularly in spinal cord injury models, where transplanted cells...
Dai-Yi Yang· International Journal of Bio...· 0 citations
Human-induced pluripotent stem cell-derived cardiomyocytes (iPSC-CMs) have revolutionized cardiac research and medicine by offering patient-specific platforms for disease modeling, drug discovery, and regenerative therapies. The ability of iPSC-CMs to replicate key aspects of human cardiac physiology makes them invalua...
Keshav Narayan Alagarsamy, Emilee Bueckert, Mehak Gupta et al.· Biochimica et Biophysica Act...· 0 citations
It is demonstrated that correction of BCOR mutation by CRISPR–Cas9 only partially restores the wildtype molecular state, highlighting the importance of early detection and monitoring of adaptive mutations in hiPSC cultures.
C. Badja, S. Boushaki, Yogesh Kumar et al.· bioRxiv· 0 citations
Background The clinical efficacy of anticancer drugs is often limited by dose-dependent toxicity to normal cells, particularly to rapidly dividing stem and progenitor cell populations. Traditional preclinical toxicity screening relies on animal models or primary human cells/immortalized lines, both of which have signif...
K. Vincze, N. Varga, Szilárd Tóth et al.· Pathology oncology research...· 0 citations
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