Forebrain microvasculature is defective in Alzheimer's disease. To model the role of cranial pericytes in influencing endothelial cell functions, we developed a method for cranial-pericyte derivation from iPSCs. Our studies reveal inherent defects in cranial pericytes from familial AD iPSC. We also demonstrate a similar pathophysiology in perimary pericytes isolated from sporadic AD patients that can be rescued. SOURCE: Ruchi Bajpai University of Southern California

Pluto Bioinformatics

GSE104141: Cranial pericytes derived from neural crest cells reveal an inherent cell type-specific defect in Alzheimer's Disease