Cholinergic neuronal activity promotes diffuse midline glioma growth through muscarinic signaling

Cell. 2025 Aug 21;188(17):4640-4657.e30. doi: 10.1016/j.cell.2025.05.031. Epub 2025 Jun 19.

Abstract

Glutamatergic neuronal activity promotes proliferation of both oligodendrocyte precursor cells (OPCs) and gliomas, including diffuse midline glioma (DMG). However, the role of neuromodulatory brainstem neurons projecting to midline structures where DMGs arise remains unexplored. Here, we demonstrate that midbrain cholinergic neuronal activity modulates OPC and DMG proliferation in a circuit-dependent manner. Optogenetic stimulation of the cholinergic pedunculopontine nucleus (PPN) promotes glioma growth in pons, while stimulation of the laterodorsal tegmentum nucleus (LDT) drives proliferation in thalamus. DMG-bearing mice exhibit higher acetylcholine release and increased cholinergic neuronal activity over the disease course. In co-culture, cholinergic neurons enhance DMG proliferation, and acetylcholine directly acts on DMG cells. Single-cell RNA sequencing revealed high CHRM1 and CHRM3 expression in primary DMG samples. Pharmacological or genetic blockade of M1/M3 receptors abolished cholinergic activity-driven DMG proliferation. Taken together, these findings demonstrate that midbrain cholinergic long-range projections promote activity-dependent DMG growth, mirroring a parallel proliferative effect on healthy OPCs.

Keywords: DMG; LDT; OPC; PPN; cholinergic neuron; diffuse midline glioma; glioma; laterodorsal tegmentum nucleus; neuron; neuron-glioma; neuronal activity; oligodendrocyte; oligodendrogenesis; pedunculopontine nucleus.

MeSH terms

  • Acetylcholine / metabolism
  • Animals
  • Brain Neoplasms* / metabolism
  • Brain Neoplasms* / pathology
  • Cell Proliferation
  • Cholinergic Neurons* / metabolism
  • Female
  • Glioma* / metabolism
  • Glioma* / pathology
  • Humans
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Pedunculopontine Tegmental Nucleus / metabolism
  • Receptor, Muscarinic M1 / metabolism
  • Receptor, Muscarinic M3 / metabolism
  • Receptors, Muscarinic* / genetics
  • Receptors, Muscarinic* / metabolism
  • Signal Transduction

Substances

  • Acetylcholine
  • Receptors, Muscarinic
  • Receptor, Muscarinic M3
  • Receptor, Muscarinic M1