Evidence map›Paper›PMID 34006329›Full record

ArticleActa neuropathologica communications2021

VISTA regulates microglia homeostasis and myelin phagocytosis, and is associated with MS lesion pathology.

Malte Borggrewe, Susanne M Kooistra, Evelyn M Wesseling, Fenja L Gierschek, Maaike L Brummer, Elizabeth C Nowak, Tiago Medeiros-Furquim, Tegan A Otto, Sam W Lee, Randolph J Noelle and 2 more

Open access · goldAbstract read
In one paragraph

Article in Acta neuropathologica communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 15 citations in OpenAlex.

  1. Pervasive Somatic Mutations inbioRxiv : the preprint server for biology · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Malte BorggreweDepartment of Biomedical Sciences of Cells and Systems, Section Molecular Neurobiology, University Medical Center Groningen, University of Groningen, and MS Centrum Noord Nederland (MSCNN), Groningen, The Netherlands.
Susanne M KooistraDepartment of Biomedical Sciences of Cells and Systems, Section Molecular Neurobiology, University Medical Center Groningen, University of Groningen, and MS Centrum Noord Nederland (MSCNN), Groningen, The Netherlands.
Evelyn M WesselingDepartment of Biomedical Sciences of Cells and Systems, Section Molecular Neurobiology, University Medical Center Groningen, University of Groningen, and MS Centrum Noord Nederland (MSCNN), Groningen, The Netherlands.
Fenja L GierschekDepartment of Biomedical Sciences of Cells and Systems, Section Molecular Neurobiology, University Medical Center Groningen, University of Groningen, and MS Centrum Noord Nederland (MSCNN), Groningen, The Netherlands.
Maaike L BrummerDepartment of Biomedical Sciences of Cells and Systems, Section Molecular Neurobiology, University Medical Center Groningen, University of Groningen, and MS Centrum Noord Nederland (MSCNN), Groningen, The Netherlands.
Elizabeth C NowakDepartment of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Norris Cotton Cancer Center, Lebanon, NH, USA.
Tiago Medeiros-FurquimDepartment of Biomedical Sciences of Cells and Systems, Section Molecular Neurobiology, University Medical Center Groningen, University of Groningen, and MS Centrum Noord Nederland (MSCNN), Groningen, The Netherlands.
Tegan A OttoDepartment of Biomedical Sciences of Cells and Systems, Section Molecular Neurobiology, University Medical Center Groningen, University of Groningen, and MS Centrum Noord Nederland (MSCNN), Groningen, The Netherlands.
Sam W LeeYale University School of Medicine, New Haven, CT, USA.
Randolph J NoelleDepartment of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Norris Cotton Cancer Center, Lebanon, NH, USA.
Bart J L EggenDepartment of Biomedical Sciences of Cells and Systems, Section Molecular Neurobiology, University Medical Center Groningen, University of Groningen, and MS Centrum Noord Nederland (MSCNN), Groningen, The Netherlands.
Jon D LamanDepartment of Biomedical Sciences of Cells and Systems, Section Molecular Neurobiology, University Medical Center Groningen, University of Groningen, and MS Centrum Noord Nederland (MSCNN), Groningen, The Netherlands. j.d.laman@umcg.nl.ORCID 0000-0001-5085-9807
University Medical Center Groningen · NLDartmouth College · USYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

V-type immunoglobulin domain-containing suppressor of T-cell activation (VISTA) is a negative checkpoint regulator (NCR) that is involved in T-cell quiescence, inhibition of T-cell activation, and in myeloid cells regulates cytokine production, chemotaxis, phagocytosis, and tolerance induction. In the central nervous system (CNS), VISTA is expressed by microglia, the resident macrophage of the parenchyma, and expression is decreased during neuroinflammation; however, the function of VISTA in microglia is unknown. Here, we extensively analyzed VISTA expression in different MS lesion stages and characterized the function of VISTA in the CNS by deleting VISTA in microglia. VISTA is differentially expressed in distinct MS lesion stages. In mice, VISTA deletion in Cx3Cr1-expressing cells induced a more amoeboid microglia morphology, indicating an immune-activated phenotype. Expression of genes associated with cell cycle and immune-activation was increased in VISTA KO microglia. In response to LPS and during experimental autoimmune encephalomyelitis (EAE), VISTA KO and WT microglia shared similar transcriptional profiles and VISTA deletion did not affect EAE disease progression or microglia responses. VISTA KO in microglia in vitro decreased the uptake of myelin. This study demonstrates that VISTA is involved in microglia function, which likely affects healthy CNS homeostasis and neuroinflammation.

Indexed as

AnimalsAnimals, NewbornCells, CulturedEncephalomyelitis, Autoimmune, ExperimentalFemaleHomeostasisHumansJurkat CellsMaleMembrane ProteinsMiceMice, 129 StrainMice, Inbred C57BLMice, KnockoutMicrogliaMultiple SclerosisMembrane ProteinsVsir protein, mouseCheckpoint inhibitionDemyelinationGlial cellsImmunotherapyNeurodegenerationPD-1H

Identifiers

PMID34006329
PMCPMC8130385
OpenAlexW3160545496

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.