Ethanol modulation of cerebellar neuroinflammation in a postnatal mouse model of fetal alcohol spectrum disorders. Issue 8 (2nd February 2021)

• Record Type: Journal Article
• Authors: Kane, Cynthia J. M.; Douglas, James C.; Rafferty, Tonya; Johnson, Jennifer W.; Niedzwiedz‐Massey, Victoria M.; Phelan, Kevin D.; Majewska, Ania Katarzyna; Drew, Paul D.
• Other Names: Marshall S. Alex guestEditor.
• Is Part Of: Journal of neuroscience research. Volume 99:Issue 8(2021)
• Page Start: 1986
• Page End: 2007
• Publication Date: 2021-02-02
• Subjects: FASD -- fractalkine -- microglia -- neuroinflammation -- RRID:AB_839504 -- RRID:IMSR_JAX:000664 -- RRID:SCR_016788 -- RRID:SCR_018042 -- RRID:SCR_018064 -- RRID:SCR_018453; Neurobiology -- Periodicals; 612
• DOI: 10.1002/jnr.24797
• Languages: English
• ISSNs: 0360-4012

Abstract

Abstract: Fetal alcohol spectrum disorders (FASD) are alarmingly common, result in significant personal and societal loss, and there is no effective treatment for these disorders. Cerebellar neuropathology is common in FASD and causes aberrant cognitive and motor function. Ethanol‐induced neuroinflammation is believed to contribute to neuropathological sequelae of FASD, and was previously demonstrated in the cerebellum in animal models of FASD. We now demonstrate neuroinflammation persists in the cerebellum several days following cessation of ethanol treatment in an early postnatal mouse model, with meaningful implications for timing of therapeutic intervention in FASD. We also demonstrate by Sholl analysis that ethanol decreases ramification of microglia cell processes in cells located near the Purkinje cell layer but not those near the external granule cell layer. Ethanol did not alter the expression of anti‐inflammatory molecules or molecules that constitute NLRP1 and NLRP3 inflammasomes. Interestingly, ethanol decreased the expression of IL‐23a (P19) and IL‐12Rβ1 suggesting that ethanol may suppress IL‐12 and IL‐23 signaling. Fractalkine‐fractalkine receptor (CX3CL1‐CX3CR1) signaling is believed to suppress microglial activation and our demonstration that ethanol decreases CX3CL1 expression suggests that ethanol modulation of CX3CL1‐CX3CR1 signaling may contribute to cerebellar neuroinflammation and neuropathology. We demonstrate ethanol alters the expression of specific molecules in the cerebellum understudied in FASD, but crucial for immune responses. Ethanol increases the expression of NOX‐2 and NGP and decreases the expression of RAG1, NOS1, CD59a, S1PR5, PTPN22, GPR37, and Serpinb1b. These molecules represent a new horizon as potential targets for development of FASD therapy. Abstract : Postnatal exposure to ethanol resulted in pro‐inflammatory molecule expression in mouse cerebellum that persisted for several days suggesting that anti‐inflammatory agents may be effective in treating infants with FASD. Cerebellar microglial ramification and novel immune molecules were differentially regulated by ethanol. We demonstrate novel mechanisms for ethanol modulation of neuroinflammation.