Type of glial cellOriginAppearanceFunctions
AstrocytesNeuroectodermRound vesicular nuclei
Contain glial fibrils, composed of glial fibrillary acidic protein
• Repair
• Structural & metabolic support
• Blood-brain barrier
Remove excess neurotransmitters, related with Hyperammonemia
OligodendrocytesNeuroectodermSmall nuclei surrounded by a pale halo
Fewer processes than astrocytes
• Myelinate axons in the CNS, including CN II
• Main glial cells in the cerebral white matter
MicrogliaPrimitive yolk sac macrophagesSmall elongated nuclei
Many short branching processes
Special macrophages in CNS, i.e. phagocytic
Ependymal cellsNeuroepithelial cells (neuroectoderm)Simple columnar glial cellsForm the epithelium lining the ventricles and central canal of the spinal cord

Mnemonic

Glial cells guard the axons of the nerve cells as COPS: CNS axons are myelinated by Oligodendrocytes; PNS axons are insulated by Schwann cells. Oligodendrocytes → multiple sclerosis Schwann cells → Guillain-Barré syndrome


CNS Glial Cells

  • Astrocytes

    • Function: Most abundant glial cell in the CNS. They provide structural and metabolic support, form the blood-brain barrier (BBB), regulate the extracellular environment by taking up K+ and neurotransmitters (e.g., glutamate), and contribute to scar formation (gliosis) after injury.
    • Key Features: Star-shaped cells. Marker: Glial Fibrillary Acidic Protein (GFAP). Communicate via gap junctions.
    • Clinical Correlation: Glioblastoma Multiforme (GBM) is the most common and aggressive primary brain tumor in adults, composed of astrocytes. It can cross the corpus callosum, creating a “butterfly glioma” appearance on MRI. Reactive gliosis is the brain’s response to traumatic injury.
  • Oligodendrocytes

    • Function: Myelinate axons in the CNS. A single oligodendrocyte can myelinate multiple axons (up to 30-50).
    • Key Features: Derived from the neuroectoderm. On histology, they often have a “fried egg” appearance with a round nucleus and clear cytoplasm.
    • Clinical Correlations:
      • Damaged in demyelinating diseases like Multiple Sclerosis (MS).
      • Also affected in progressive multifocal leukoencephalopathy (PML) and leukodystrophies.
      • Oligodendrogliomas are slow-growing tumors, often found in the frontal lobes.
  • Microglia

    • Function: Act as the resident macrophages of the CNS, responsible for phagocytosis of debris, damaged cells, and pathogens. They are involved in immune surveillance and synaptic pruning.
    • Key Features: Originate from the mesoderm (yolk sac). When activated by injury or inflammation, they change shape and proliferate.
    • Clinical Correlation: Microglia are activated in response to CNS injury and infection. They play a role in neurodegenerative diseases like Alzheimer’s.
  • Ependymal Cells

    • Function: Line the ventricles of the brain and the central canal of the spinal cord. Their cilia help to circulate cerebrospinal fluid (CSF), and they participate in its production.
    • Key Features: Ciliated simple columnar or cuboidal epithelial-like cells. Form a somewhat permeable barrier between CSF and the brain parenchyma.
    • Clinical Correlation: Ependymomas are glial tumors that most commonly arise in the 4th ventricle in children.

PNS Glial Cells

  • Schwann Cells

    • Function: Myelinate axons in the PNS. One Schwann cell myelinates only one segment of a single axon. They also aid in nerve regeneration after injury.
    • Key Features: Derived from the neural crest.
    • Clinical Correlations:
      • Destroyed in Guillain-Barré syndrome, an acute inflammatory demyelinating polyneuropathy.
      • Schwannomas are benign tumors of Schwann cells. A common example is a vestibular schwannoma (acoustic neuroma) at the cerebellopontine angle, which is S-100 positive.
  • Satellite Cells

    • Function: Surround the cell bodies of neurons in sensory and autonomic ganglia, providing support and regulating the microenvironment. Their function is analogous to astrocytes in the CNS.
    • Key Features: Small cells closely associated with neuron cell bodies in the PNS.