Table 2.
Therapeutic and mechanistic methods of targeting inflammatory astrocytes.
Disease | Method | Primary target | Model system |
---|---|---|---|
Alzheimer’s Disease | Activation of melanocortin receptor by D-Tyrosine (Lau et al., 2021). | Astrocytes | in vivo |
Alzheimer’s Disease | Exercise (Belarbi et al., 2011; Nakanishia et al., 2021). | Astrocytes | in vivo |
Amyloid Lateral Sclerosis | Intrathecal transplantation of human-grade astrocytes (Izrael et al., 2020). | Astrocytes | in vivo (mouse and human) |
Glaucoma Associated Neurodegeneration | Preventing microglial release of IL-1α, TNFα, and C1q by NLY01 (Sterling et al., 2020). | Microglia | in vivo |
Huntington’s Disease | Transcriptional repression of mutant huntingtin protein using zinc finger proteins (Diaz-Castro et al., 2019). | Astrocytes | in vivo |
Parkinson’s Disease | Dopamine D2 receptor agonist inhibition of NLRP3 inflammasome activation in astrocytes (Zhu et al., 2018). | Astrocytes | in vivo |
Parkinson’s Disease | Genetic deletion of Kir6.2 (Song et al., 2021). | Astrocytes | in vivo |
Parkinson’s Disease | Prevent microglial release of IL-1α, TNFα, and C1q by NLY01 (Yun et al., 2018). | Microglia | in vitro/in vivo |
Prion Disease | Genetic deletion of TNFα, IL-1α, and C1q triple KO (Hartmann et al., 2019). | Microglia | in vivo |
Multiple Sclerosis | NLRP3 inflammasome inhibition (Hou et al., 2020). | Astrocytes | in vivo |