4.5 Article

Alcohol alters IL-6 Signal Transduction in the CNS of Transgenic Mice with Increased Astrocyte Expression of IL-6

Journal

CELLULAR AND MOLECULAR NEUROBIOLOGY
Volume 41, Issue 4, Pages 733-750

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10571-020-00879-2

Keywords

STAT3; C; EPB beta; p42; 44 MAPK; Glia; GFAP; Chronic intermittent alcohol

Funding

  1. National Institutes of Health [AA024484]
  2. Integrated Neuroscience Initiative on Alcoholism (INIA)-West grant [AA020893]
  3. Scripps Research Institute's Mouse Behavioral Assessment Core

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Neuroimmune factors, such as IL-6, play crucial roles in regulating CNS function under physiological and pathological conditions. Elevated IL-6 expression in the CNS is associated with disorders like excessive alcohol use, affecting cerebellar function by altering gene expression. Interactions between IL-6 and alcohol can modify IL-6 signal transduction partners, potentially contributing to cerebellar actions of alcohol.
Neuroimmune factors, including the cytokine interleukin-6 (IL-6), are important chemical regulators of central nervous system (CNS) function under both physiological and pathological conditions. Elevated expression of IL-6 occurs in the CNS in a variety of disorders associated with altered CNS function, including excessive alcohol use. Alcohol-induced production of IL-6 has been reported for several CNS regions including the cerebellum. Cerebellar actions of alcohol occur through a variety of mechanisms, but alcohol-induced changes in signal transduction, transcription, and translation are known to play important roles. IL-6 is an activator of signal transduction that regulates gene expression. Thus, alcohol-induced IL-6 production could contribute to cerebellar effects of alcohol by altering gene expression, especially under conditions of chronic alcohol abuse, where IL-6 levels could be habitually elevated. To gain an understanding of the effects of alcohol on IL-6 signal transduction, we studied activation/expression of IL-6 signal transduction partners STAT3 (Signal Transducer and Activator of Transcription), CCAAT-enhancer binding protein (C/EBP) beta, and p42/p44 mitogen-activated protein kinase (MAPK) at the protein level. Cerebella of transgenic mice that express elevated levels of astrocyte produced IL-6 in the CNS were studied. Results show that the both IL-6 and chronic intermittent alcohol exposure/withdrawal affect IL-6 signal transduction partners and that the actions of IL-6 and alcohol interact to alter activation/expression of IL-6 signal transduction partners. The alcohol/IL-6 interactions may contribute to cerebellar actions of alcohol, whereas the effects of IL-6 alone may have relevance to cerebellar changes occurring in CNS disorders associated with elevated levels of IL-6.

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