[HTML][HTML] ActivinA induced SMAD1/5 signaling in an iPSC derived EC model of fibrodysplasia ossificans progressiva (FOP) can be rescued by the drug candidate …

S Hildebrandt, B Kampfrath, K Fischer… - Stem Cell Reviews and …, 2021 - Springer
S Hildebrandt, B Kampfrath, K Fischer, L Hildebrand, J Haupt, H Stachelscheid, P Knaus
Stem Cell Reviews and Reports, 2021Springer
Balanced signal transduction is crucial in tissue patterning, particularly in the vasculature.
Heterotopic ossification (HO) is tightly linked to vascularization with increased vessel
number in hereditary forms of HO, such as Fibrodysplasia ossificans progressiva (FOP). FOP
is caused by mutations in the BMP type I receptor ACVR1 leading to aberrant SMAD1/5
signaling in response to ActivinA. Whether observed vascular phenotype in human FOP
lesions is connected to aberrant ActivinA signaling is unknown. Blocking of ActivinA …
Abstract
Balanced signal transduction is crucial in tissue patterning, particularly in the vasculature. Heterotopic ossification (HO) is tightly linked to vascularization with increased vessel number in hereditary forms of HO, such as Fibrodysplasia ossificans progressiva (FOP). FOP is caused by mutations in the BMP type I receptor ACVR1 leading to aberrant SMAD1/5 signaling in response to ActivinA. Whether observed vascular phenotype in human FOP lesions is connected to aberrant ActivinA signaling is unknown. Blocking of ActivinA prevents HO in FOP mice indicating a central role of the ligand in FOP. Here, we established a new FOP endothelial cell model generated from induced pluripotent stem cells (iECs) to study ActivinA signaling. FOP iECs recapitulate pathogenic ActivinA/SMAD1/5 signaling. Whole transcriptome analysis identified ActivinA mediated activation of the BMP/NOTCH pathway exclusively in FOP iECs, which was rescued to WT transcriptional levels by the drug candidate Saracatinib. We propose that ActivinA causes transcriptional pre-patterning of the FOP endothelium, which might contribute to differential vascularity in FOP lesions compared to non-hereditary HO.
Graphical abstract
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