Table 3.
Cell Lines | |||
---|---|---|---|
Cell Lines | Associated Cell Type and Tumor | Detailed Example | References |
Derived from tumor | |||
SH-SY5Y (also SH-SY6Y) cells | Neurons (cholinergic neurons after differentiation), derived from a neuroblastoma | In 3D culture, SH-SY5Y cells were used to model an AD-like tauopathy, induced with okadaic acid and the recombinant mutated human tau [121]. | 2D: [16,113,122,123,124] 3D: [121,125] |
SK-N-MC cells | Neurons, derived from a neuroepithelioma | Aβ-treated SK-N-MC cells were used to find efficient drugs able to cross the BBB and rescue the degenerating neurons from apoptosis. | [107] |
SK-N-SH cells | Neurons, derived from a neuroblastoma | Treatment of SK-N-SH with Aβ25-35 peptides was used to model AD in vitro. With this model, Gu et al. (2020) investigated genes and proteins involved in cell death during AD, identifying pathways to improve cell viability. | [126] |
BE(2)-M17 cells | Neurons, derived from a neuroblastoma | Su et al. (2010) studied the role of chronic oxidative stress on tau hyperphosphorylation with a M17-based cellular stress model. They showed that stress increases tau phosphorylation in vitro and suggested a role in neurofibrillary pathology in vivo. | [127] |
PC-12 cells | Chromaffin cells (modified neurons), derived from a pheochromocytoma | The neuroprotective effects of two marine-derived carotenoids was assessed with Aβ1-42-treated PC-12 cells [40]. | [40,121,128] |
7W-CHO cells | Chinese ovary cells overexpressing the human APP gene | 7W-CHO cells were used to screen drugs able to increase the ratio between sAPPα, a neurite extending fragment, and Aβ peptides, which are neurite retractive [129]. | [129,130] |
CALU-3 cells | Epithelial cells, from an adenocarcinoma | CALU-3 cells were used to measure drug delivery through epithelium of a β-sheet breaker [131]. | [131,132] |
Immortalized with a viral vector | |||
ReN cells and immortalized microglial cells | Neural stem cells and microglial cells | Park et al. (2018) engineered a 3D triculture system as a model of AD neurodegeneration and neuroinflammation. They notably cultured fAD-mutated ReN cells, which are neural progenitor cells, and induced their differentiation into Aβ-overexpressing neurons and astrocytes. They also added immortalized microglial cells, completing the triculture system [133]. | [133,134] |
Immortalized brain endothelial cells | Endothelial cells | Endothelial cells were used to model Aβ clearance through BBB [135]. | Human cells: [135,136] Mouse cells: [137] |
HEK293 cells | Embryonic kidney cells | Waxman and Giasson (2011) developed a cellular model to study the induction of tau aggregation with preformed α-synuclein fibrils, another protein involved in Parkinson’s disease [138]. | [138,139] |