How omics is revealing new roles for glia in addiction.
David J BergkampJohn F NeumaierPublished in: Glia (2024)
Experiments to study the biology of addiction have historically focused on the mechanisms through which drugs of abuse drive changes in the functioning of neurons and neural circuits. Glia have often been ignored in these studies, however, and this has left many questions in the field unanswered, particularly, surrounding how glia contribute to changes in synaptic plasticity, regulation of neuroinflammation, and functioning of neural ensembles given massive changes in signaling across the CNS. Omics methods (transcriptomics, translatomics, epigenomics, proteomics, metabolomics, and others) have expanded researchers' abilities to generate hypotheses and carry out mechanistic studies of glial cells during acquisition of drug taking, intoxication, withdrawal, and relapse to drug seeking. Here, we present a survey of how omics technological advances are revising our understanding of astrocytes, microglia, oligodendrocytes, and ependymal cells in addiction biology.
Keyphrases
- induced apoptosis
- single cell
- cell cycle arrest
- mass spectrometry
- endoplasmic reticulum stress
- spinal cord
- cell death
- emergency department
- oxidative stress
- blood brain barrier
- signaling pathway
- cognitive impairment
- lipopolysaccharide induced
- spinal cord injury
- brain injury
- subarachnoid hemorrhage
- electronic health record