VISTA expression by microglia decreases during inflammation and is differentially regulated in CNS diseases

Borggrewe, M., Grit, C., Den Dunnen, W. F. A., Burm, S. M., Bajramovic, J. J., Noelle, R. J., Eggen, B. J. L. & Laman, J. D., Dec-2018, In : Glia. 66, 12, p. 2645-2658 14 p.

Research output: Contribution to journalArticleAcademicpeer-review

V-type immunoglobulin domain-containing suppressor of T-cell activation (VISTA) is a negative checkpoint regulator (NCR) involved in inhibition of T cell-mediated immunity. Expression changes of other NCRs (PD-1, PD-L1/L2, CTLA-4) during inflammation of the central nervous system (CNS) were previously demonstrated, but VISTA expression in the CNS has not yet been explored. Here, we report that in the human and mouse CNS, VISTA is most abundantly expressed by microglia, and to lower levels by endothelial cells. Upon TLR stimulation, VISTA expression was reduced in primary neonatal mouse and adult rhesus macaque microglia in vitro. In mice, microglial VISTA expression was reduced after lipopolysaccharide (LPS) injection, during experimental autoimmune encephalomyelitis (EAE), and in the accelerated aging Ercc1 Δ/- mouse model. After LPS injection, decreased VISTA expression in mouse microglia was accompanied by decreased acetylation of lysine residue 27 in histone 3 in both its promoter and enhancer region. ATAC-sequencing indicated a potential regulation of VISTA expression by Pu.1 and Mafb, two transcription factors crucial for microglia function. Finally, our data suggested that VISTA expression was decreased in microglia in multiple sclerosis lesion tissue, whereas it was increased in Alzheimer's disease patients. This study is the first to demonstrate that in the CNS, VISTA is expressed by microglia, and that VISTA is differentially expressed in CNS pathologies.

Original languageEnglish
Pages (from-to)2645-2658
Number of pages14
Issue number12
Publication statusPublished - Dec-2018


  • autoimmunity, cancer, DD1alpha, immune checkpoints, immunotherapy, neurodegeneration, PD-1H, IMMUNE-CHECKPOINT BLOCKADE, MULTIPLE-SCLEROSIS, AMYLOID-BETA, CELLS, MOUSE, PATHWAY, ACTIVATION, PHENOTYPE, PATHOLOGY, RESPONSES

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