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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.<\/jats:p>","DOI":"10.1002\/glia.24584","type":"journal-article","created":{"date-parts":[[2024,6,19]],"date-time":"2024-06-19T06:50:40Z","timestamp":1718779840000},"page":"608-618","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":4,"title":["How omics is revealing new roles for glia in addiction"],"prefix":"10.1002","volume":"73","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-6314-5544","authenticated-orcid":false,"given":"David J.","family":"Bergkamp","sequence":"first","affiliation":[{"name":"Department of Pharmacology University of Washington  Seattle Washington USA"},{"name":"VISN 20 Mental Illness Research, Education and Clinical Center VA Puget Sound Health Care System  Seattle Washington 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