Evidence map›Paper›PMID 31525189›Full record

ArticlePLoS biology2019

NLRX1 inhibits the early stages of CNS inflammation and prevents the onset of spontaneous autoimmunity.

Marjan Gharagozloo, Shaimaa Mahmoud, Camille Simard, Kenzo Yamamoto, Diwakar Bobbala, Subburaj Ilangumaran, Matthew D Smith, Albert Lamontagne, Samir Jarjoura, Jean-Bernard Denault and 8 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

23 citing papers in PubMed, 36 citations in OpenAlex.

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  16. Pyroptosis in spinal cord injury.Frontiers in cellular neuroscience · 2022
    Review
  17. NOD-like receptors in autoimmune diseases.Acta pharmacologica Sinica · 2021
    Review
  18. Review
  19. Focusing on the Cell Type Specific Regulatory Actions of NLRX1.International journal of molecular sciences · 2021
    Review
  20. Article
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

18 authors at 4 institutions in 2 countries.

Marjan GharagozlooDepartment of Pharmacology and Physiology, Faculty of Medicine, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
Shaimaa MahmoudDepartment of Pharmacology and Physiology, Faculty of Medicine, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
Camille SimardDepartment of Pharmacology and Physiology, Faculty of Medicine, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
Kenzo YamamotoDepartment of Chemical Engineering and Biotechnological Engineering, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
Diwakar BobbalaDepartment of Anatomy and Cell Biology, Faculty of Medicine, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
Subburaj IlangumaranDepartment of Anatomy and Cell Biology, Faculty of Medicine, Université de Sherbrooke, Sherbrooke, Quebec, Canada.ORCID 0000-0002-7563-576X
Matthew D SmithDepartment of Neurology, Johns Hopkins University, Baltimore, Maryland, United States of America.ORCID 0000-0001-6614-569X
Albert LamontagneDepartment of Neurology, Faculty of Medicine, MS Clinic, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
Samir JarjouraDepartment of Neurology, Faculty of Medicine, MS Clinic, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
Jean-Bernard DenaultDepartment of Pharmacology and Physiology, Faculty of Medicine, Université de Sherbrooke, Sherbrooke, Quebec, Canada.ORCID 0000-0001-5392-0685
Véronique BlaisDepartment of Pharmacology and Physiology, Faculty of Medicine, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
Louis GendronDepartment of Pharmacology and Physiology, Faculty of Medicine, Université de Sherbrooke, Sherbrooke, Quebec, Canada.ORCID 0000-0002-2058-8863
Carles Vilariño-GüellDepartment of Medical Genetics, University of British Columbia, Vancouver, Canada.ORCID 0000-0002-5612-5940
A Dessa SadovnickDepartment of Medical Genetics, University of British Columbia, Vancouver, Canada.
Jenny P TingDepartment of Microbiology and Immunology, Lineberger Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States of America.ORCID 0000-0002-7846-0395
Peter A CalabresiDepartment of Neurology, Johns Hopkins University, Baltimore, Maryland, United States of America.ORCID 0000-0002-7776-6472
Abdelaziz AmraniDepartment of Pediatrics, Faculty of Medicine, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
Denis GrisDepartment of Pharmacology and Physiology, Faculty of Medicine, Université de Sherbrooke, Sherbrooke, Quebec, Canada.ORCID 0000-0003-1215-2434
Université de Sherbrooke · CAJohns Hopkins University · USUniversity of British Columbia · CAUniversity of North Carolina at Chapel Hill · US

Funding

Mechanisms by which effector T cells modulate endogenous remyelinationR37NS041435 · NINDS · JOHNS HOPKINS UNIVERSITY · PI CALABRESI, PETER A · 2013 to 2019
$3.0M
CIHR MOP-137051NINDS NIH HHS R37 NS041435
6 · The paper itself

Abstract

Nucleotide-binding, leucine-rich repeat containing X1 (NLRX1) is a mitochondria-located innate immune sensor that inhibits major pro-inflammatory pathways such as type I interferon and nuclear factor-κB signaling. We generated a novel, spontaneous, and rapidly progressing mouse model of multiple sclerosis (MS) by crossing myelin-specific T-cell receptor (TCR) transgenic mice with Nlrx1-/- mice. About half of the resulting progeny developed spontaneous experimental autoimmune encephalomyelitis (spEAE), which was associated with severe demyelination and inflammation in the central nervous system (CNS). Using lymphocyte-deficient mice and a series of adoptive transfer experiments, we demonstrate that genetic susceptibility to EAE lies within the innate immune compartment. We show that NLRX1 inhibits the subclinical stages of microglial activation and prevents the generation of neurotoxic astrocytes that induce neuronal and oligodendrocyte death in vitro. Moreover, we discovered several mutations within NLRX1 that run in MS-affected families. In summary, our findings highlight the importance of NLRX1 in controlling the early stages of CNS inflammation and preventing the onset of spontaneous autoimmunity.

Indexed as

AdultAnimalsAstrocytesCase-Control StudiesCentral Nervous SystemCodon, NonsenseDemyelinating DiseasesEncephalomyelitis, Autoimmune, ExperimentalFemaleHumansImmunity, InnateMaleMice, TransgenicMiddle AgedMitochondrial ProteinsMutation, MissenseCodon, NonsenseMitochondrial ProteinsNLRX1 protein, humanNLRX1 protein, mouse

Identifiers

PMID31525189
PMCPMC6762215
OpenAlexW2973370767

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.