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. 2020 Jan 23;45(3):643–655. doi: 10.1007/s11064-020-02961-z

Table 1.

Glial cells mechanism in cerebellar development and disease

Glial cells in the cerebellum Mechanism in celebellar development Mechanism in disease
Astrocytes

Secrete cytokines and growth factors →  oligodendrocytes and myelin modulation

Bergmann glia →  provides a structure for cerebellar neuron migration and positioning

Glial inflammation disorders

EAE → proinflammatory cytokine release (IL-1β)

SCA1 → Bergmann glial cell reactivity through NF-Κβ

Neuron–glial interaction disorders

ADHD → increased GABA levels

SCA7 → GLAST function interference, cause Purkinje cell excitotoxicity

Oxidative stress disorders

Neonatal ischemia →  increased Ca2+ influx in Bergmann cells

Oligodendrocytes

Cerebella cytoarchitecture maintenance

Oligodendrocytes–Neuron interaction maintains and forms Ranvier nodes and paranodal regions of Purkineje cell

Oxidative stress disorders

Postnatal hiperoxia → oligodendroglial maldevelopment

Postnatal hypoxia → hypomielinization and reduced oligodendroglial maturation

Microglia Regulate neurite growth, synaptic pruning, spinogenesis, neuronal apoptosis and oligodendrocyte maturation and development

Inflammation disorders

EAE → increased INFβ release

SCA1 → inflammation (increase of TNFa)

SCA3 → upregulation of (MMP-2, IL-1 and SDF1alpha)