Bergkamp David J, Neumaier John F
Department of Pharmacology, University of Washington, Seattle, Washington, USA.
VISN 20 Mental Illness Research, Education and Clinical Center, VA Puget Sound Health Care System, Seattle, Washington, USA.
Glia. 2025 Mar;73(3):608-618. doi: 10.1002/glia.24584. Epub 2024 Jun 18.
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.
从历史角度来看,研究成瘾生物学的实验主要聚焦于滥用药物促使神经元和神经回路功能发生改变的机制。然而,在这些研究中,神经胶质细胞常常被忽视,这使得该领域的许多问题悬而未决,尤其是在中枢神经系统信号发生巨大变化的情况下,神经胶质细胞如何影响突触可塑性的改变、神经炎症的调节以及神经集合体的功能。组学方法(转录组学、翻译组学、表观基因组学、蛋白质组学、代谢组学等)扩展了研究人员提出假设的能力,并使他们能够在药物摄取、中毒、戒断以及复吸寻求药物的过程中,对神经胶质细胞进行机制研究。在此,我们概述了组学技术的进步如何修正我们对成瘾生物学中星形胶质细胞、小胶质细胞、少突胶质细胞和室管膜细胞的理解。