Astrocytic A20 ameliorates experimental autoimmune encephalomyelitis by inhibiting NF-kappa B- and STAT1-dependent chemokine production in astrocytes

作者：Wang Xu; Deckert Martina; Nguyen Thi Xuan; Nishanth Gopala; Just Sissy; Waisman Ari; Naumann Michael; Schlueter Dirk

来源：Acta Neuropathologica, 2013, 126(5): 711-724.

DOI：10.1007/s00401-013-1183-9

• A20
• Astrocytes
• Autoimmunity
• EAE

Single-nucleotide polymorphisms in the tumor necrosis factor, alpha-induced protein 3 gene, which encodes the ubiquitin-modifying protein A20, are linked to susceptibility to multiple sclerosis (MS), a demyelinating autoimmune disease of the central nervous system (CNS). Since it is unresolved how A20 regulates MS pathogenesis, we examined its function in a murine model of MS, namely experimental autoimmune encephalomyelitis (EAE). Deletion of A20 in neuroectodermal cells (astrocytes, neurons, and oligodendrocytes; Nestin-Cre A20(fl/fl) mice) or selectively in astrocytes (GFAP-Cre A20(fl/fl) mice) resulted in more severe EAE as compared to control animals. In Nestin-Cre A20(fl/fl) and GFAP-Cre A20(fl/fl) mice demyelination and recruitment of inflammatory leukocytes were increased as compared to A20(fl/fl) control mice. Importantly, numbers of encephalitogenic CD4(+) T cells producing interferon (IFN)-gamma, interleukin (IL)-17, and granulocyte-macrophage colony-stimulating factor (GM-CSF), respectively, as well as mRNA production of IFN-gamma, IL-17, tumor necrosis factor (TNF), GM-CSF, IL-6, CXCL1, CCL2, and CXCL10 were significantly increased in spinal cords of Nestin-Cre A20(fl/fl) and GFAP-Cre A20(fl/fl) mice, respectively. Compared to A20-sufficient astrocytes, A20-deficient astrocytes displayed stronger activation of nuclear factor kappa-light-chain enhancer of activated B cells (NF-kappa B) in response to TNF, IL-17, and GM-CSF, and of signal transducer and activator of transcription 1 (STAT1) upon IFN-gamma stimulation. Due to NF-kappa B and STAT1 hyperactivation, A20-deficient astrocytes produced significantly more chemokines in response to these key encephalitogenic cytokines of autoimmune CD4(+) T cells resulting in an amplification of CD4(+) T cell recruitment to the CNS. Thus, astrocytic A20 is an important inhibitor of autoimmune-mediated demyelination in the CNS.

• 出版日期2013-11
• 单位河北医科大学