Glial gene networks associated with alcohol dependence

• Published in: Scientific reports 2019-07, Vol.9 (1), p.10949-13, Article 10949
• Main Authors: Erickson, Emma K., Blednov, Yuri A., Harris, R. Adron, Mayfield, R. Dayne
• Format: Article
• Language: English
• Subjects: 13/1; 13/51; 14/63; 38/39; 45/90; 45/91; 631/114/2114; 631/378/1689/5; 631/378/2596; 64/60; Abuse; Adaptation; Addictions; Alcohol; Alcohol abuse; Alcoholism - genetics; Alcohols; Animals; Astrocytes; Astrocytes - metabolism; Astrocytes - pathology; Calcium signalling; Drug addiction; Drug dependence; Ethanol; Ethanol - metabolism; Functional anatomy; Gene expression; Gene Regulatory Networks; Glial cells; Humanities and Social Sciences; Inflammation; Interferon; Male; Mice; Mice, Inbred C57BL; Microglia; Microglia - metabolism; Microglia - pathology; multidisciplinary; Phenotypes; Prefrontal cortex; Prefrontal Cortex - metabolism; Prefrontal Cortex - pathology; Ribonucleic acid; RNA; RNA-Seq; Science; Science (multidisciplinary); Signal transduction; Structure-function relationships; Transcriptome
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-019-47454-4

Chronic alcohol abuse alters the molecular structure and function of brain cells. Recent work suggests adaptations made by glial cells, such as astrocytes and microglia, regulate physiological and behavioral changes associated with addiction. Defining how alcohol dependence alters the transcriptome of different cell types is critical for developing the mechanistic hypotheses necessary for a nuanced understanding of cellular signaling in the alcohol-dependent brain. We performed RNA-sequencing on total homogenate and glial cell populations isolated from mouse prefrontal cortex (PFC) following chronic intermittent ethanol vapor exposure (CIE). Compared with total homogenate, we observed unique and robust gene expression changes in astrocytes and microglia in response to CIE. Gene co-expression network analysis revealed biological pathways and hub genes associated with CIE in astrocytes and microglia that may regulate alcohol-dependent phenotypes. Astrocyte identity and synaptic calcium signaling genes were enriched in alcohol-associated astrocyte networks, while TGF-β signaling and inflammatory response genes were disrupted by CIE treatment in microglia gene networks. Genes related to innate immune signaling, specifically interferon pathways, were consistently up-regulated across CIE-exposed astrocytes, microglia, and total homogenate PFC tissue. This study illuminates the cell-specific effects of chronic alcohol exposure and provides novel molecular targets for studying alcohol dependence.