Disease modelled | Organoid type | Cell type | Phenotype | References |
---|---|---|---|---|
Timothy syndrome | Assembloids (dorsal and ventral forebrain) | GABAergic interneuron | Abnormal saltation frequency and shorter saltation length | Birey et al., 2017 [32] |
Miller–Dieker syndrome | Forebrain | Ventricular zone radial glial cells (vRGCs) | Decreased neuroepithelial loops with distorted cortical niche, abnormal vRG cell division, reduced size of organoids | Iefremova et al., 2017 [74], Bershteyn, M. et al., 2017 [44], Karzburn et al., 2018 [75] |
Zika virus infection (ZIKV) | Forebrain | Neuronal progenitors | Smaller size organoids with larger ventricular lumen and reduced neuronal cell-layer thickness, increase ZIKV-induced cell apoptosis | |
Cytomegalovirus infection (CMV) | Dorsal forebrain | Neuronal progenitors | Decreased cellular proliferation, marred cortical lamination necrosis, induced-vacuolar and cystic degeneration | |
Herpes simplex virus (HSV) | Neurosphere | Neurons | Vulnerability of matured neurons (MAP2 +) to destruction via lysis of HSV-1 | D’Aiuto et al., 2019 [80] |
Autism spectrum disorder | Dorsal forebrain | GABA/Glutamate neuron | Increased generation of NPCs and GABAergic neurons, overexpression of FOXG1 | |
Alzheimer’s disease (AD) | Dorsal Forebrain | Neurons | Induced amyloid aggregation, hyperphosphorylated tau protein and endosome abnormalities | Raja et al., 2016 [83], Pavoni, S. et al., 2018 [84], Papaspyropoulos, A. et al., 2020 [85] |
Tuberous sclerosis complex (TSC) | Forebrain | Neuronal progenitors, neurons | A strong bias astro-glial fate generation, altered cellular morphology, activation of Mtorc1 signaling | Blair, J. D.et al., 2018 [86] |