Pluripotent stem-cell-based screening uncovers sildenafil as a mitochondrial disease therapy
Summary
Mitochondrial disease encompasses inherited disorders affecting mitochondrial function. A severe and untreatable form of mitochondrial disease is Leigh syndrome (LS), causing psychomotor regression and metabolic crises. To accelerate drug discovery for LS, we screen a library of 5,632 repurposable compounds in neural cells from LS-patient-derived induced pluripotent stem cells (iPSCs). We identify phosphodiesterase type 5 (PDE5) inhibitors as leads and prioritize sildenafil for its clinica
Content
# Pluripotent stem-cell-based screening uncovers sildenafil as a mitochondrial disease therapy
*Published: 2026 Mar 19*
Mitochondrial disease encompasses inherited disorders affecting mitochondrial
function. A severe and untreatable form of mitochondrial disease is Leigh
syndrome (LS), causing psychomotor regression and metabolic crises. To
accelerate drug discovery for LS, we screen a library of 5,632 repurposable
compounds in neural cells from LS-patient-derived induced pluripotent stem cells
(iPSCs). We identify phosphodiesterase type 5 (PDE5) inhibitors as leads and
prioritize sildenafil for its clinical safety. Sildenafil corrects mitochondrial
membrane potential defects, restores neurodevelopmental pathways, and normalizes
calcium responses in LS brain organoids. In small and large mammalian models of
LS, sildenafil extends lifespan and ameliorates disease phenotypes. Off-label
treatment on an individual basis with sildenafil in six LS patients improves
their motor function and resistance to metabolic crises. Collectively, the
findings highlight the potential of iPSC-driven drug discovery and position
sildenafil as a promising drug candidate for mitochondrial disease.
DOI: 10.1016/j.cell.2026.02.008