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Alcohol Clin Exp Res ; 46(1): 29-39, 2022 01.
Article in English | MEDLINE | ID: mdl-34839533

ABSTRACT

BACKGROUND: Chloride intracellular channel 4 (CLIC4) is a multifunctional metamorphic protein for which a growing body of evidence supports a major role in the brain's molecular and behavioral responses to ethanol (EtOH). Although key to understanding the functional biology underlying this role, little is known about the cellular and subcellular expression patterns of CLIC4 in brain and how they are affected by EtOH. METHODS: We used qRT-PCR to assess Clic4 mRNA expression in the medial prefrontal cortex (mPFC) of C57BL/6J mice in the absence and presence of acute EtOH exposure. Two complementary immunohistochemical techniques were employed to assess the subcellular localization of the CLIC4 protein and its pattern of expression across brain cell types in the mPFC in the absence and presence of acute EtOH. RESULTS: Through immunohistochemical and stereological techniques, we show that CLIC4 protein is robustly expressed by oligodendrocytes (most abundant), microglia, and astrocytes, with minimal expression in neurons. Following acute EtOH exposure, we observed a rapid increase in Clic4 mRNA expression in female but not male mice and an overall increase in the number of oligodendrocytes and astrocytes expressing the CLIC4 protein. CONCLUSIONS: These findings suggest that Clic4 functions as an early response gene for acute EtOH in brain, which likely underlies its ability to modulate EtOH behavior. Our results also suggest that the role of CLIC4 in the brain's response to EtOH is mediated through oligodendrocytes.


Subject(s)
Chloride Channels/genetics , Ethanol/pharmacology , Gene Expression Regulation/drug effects , Mitochondrial Proteins/genetics , Prefrontal Cortex/metabolism , Transcriptome/drug effects , Animals , Astrocytes/metabolism , Astrocytes/ultrastructure , Behavior, Animal/drug effects , Chloride Channels/analysis , Chloride Channels/physiology , Female , Male , Mice , Mice, Inbred C57BL , Mitochondrial Proteins/analysis , Mitochondrial Proteins/physiology , Oligodendroglia/metabolism , Prefrontal Cortex/chemistry , Prefrontal Cortex/drug effects , RNA, Messenger/analysis , Sex Characteristics
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