Evidence map›Paper›PMID 26148848›Full record

ArticleASN neuro

Epigenetic Modulation of Microglial Inflammatory Gene Loci in Helminth-Induced Immune Suppression: Implications for Immune Regulation in Neurocysticercosis.

Arun Chauhan, Fredice Z Quenum, Ata Abbas, David S Bradley, Sergei Nechaev, Brij B Singh, Jyotika Sharma, Bibhuti B Mishra

Open access · goldAbstract read
In one paragraph

Article in ASN neuro. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
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  7. Article
  8. Frontiers in immunology · 2021
    Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Dopaminergic neurotoxins induce cell death by attenuating NF-κB-mediated regulation of TRPC1 expression and autophagy.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  15. Review
  16. Helminths in the gastrointestinal tract as modulators of immunity and pathology.American journal of physiology. Gastrointestinal and liver physiology · 2017
    Review
  17. Review
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

8 authors at 1 institution in 1 country.

Arun ChauhanDepartment of Basic Sciences, School of Medicine and Health Sciences, The University of North Dakota, Grand Forks, ND, USA.
Fredice Z QuenumDepartment of Basic Sciences, School of Medicine and Health Sciences, The University of North Dakota, Grand Forks, ND, USA.
Ata AbbasDepartment of Basic Sciences, School of Medicine and Health Sciences, The University of North Dakota, Grand Forks, ND, USA.
David S BradleyDepartment of Basic Sciences, School of Medicine and Health Sciences, The University of North Dakota, Grand Forks, ND, USA.
Sergei NechaevDepartment of Basic Sciences, School of Medicine and Health Sciences, The University of North Dakota, Grand Forks, ND, USA.
Brij B SinghDepartment of Basic Sciences, School of Medicine and Health Sciences, The University of North Dakota, Grand Forks, ND, USA.
Jyotika SharmaDepartment of Basic Sciences, School of Medicine and Health Sciences, The University of North Dakota, Grand Forks, ND, USA.
Bibhuti B MishraDepartment of Basic Sciences, School of Medicine and Health Sciences, The University of North Dakota, Grand Forks, ND, USA bibhuti.mishra@med.und.edu.
University of North Dakota · US

Funding

TRPC1, Calcium, and Saliva SecretionR01DE017102 · NIDCR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Brij B Singh · 2006 to 2026
$7.5M
Pilot Projects CoreP30GM103329 · NIGMS · UNIVERSITY OF NORTH DAKOTA · PI GEIGER, JONATHAN DAVID · 2012 to 2016
$5.1M
Identification of protective proteins of Francisella using a novel comparative imR21AI107457 · NIAID · UNIVERSITY OF NORTH DAKOTA · PI SHARMA, JYOTIKA · 2014 to 2015
$388k
Mechanism of sepsis development in pulmonary bacterial infectionR21AI101644 · NIAID · UNIVERSITY OF NORTH DAKOTA · PI SHARMA, JYOTIKA · 2012 to 2013
$387k
NIAID NIH HHS 1R21AI101644-01NIAID NIH HHS 1R21AI107457-01A1NIAID NIH HHS R21 AI107457NIDCR NIH HHS R01 DE017102NIGMS NIH HHS P30 GM103329NIGMS NIH HHS P30GM103329
6 · The paper itself

Abstract

In neurocysticercosis, parasite-induced immune suppressive effects are thought to play an important role in enabling site-specific inhibition of inflammatory responses to infections. It is axiomatic that microglia-mediated (M1 proinflammatory) response causes central nervous system inflammation; however, the mechanisms by which helminth parasites modulate microglia activation remain poorly understood. Here, we show that microglia display a diminished expression of M1-inflammatory mediators such as tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6), and nitric oxide synthase 2 (NOS2) in murine neurocysticercosis. Microglia also exhibited a lack of myeloid cell maturation marker major histocompatibility complex (MHC)-II in these parasite-infected brains. Treatment of microglia with helminth soluble/secreted factors (HSFs) in vitro did not induce expression of M1-inflammatory signature molecule NOS2 as well as MHC-II in primary microglia. However, HSF treatment completely inhibited lipopolysaccharide-induced increase in expression of MHC-II, NOS2 and nitric oxide production in these cells. As epigenetic modulation of chromatin states that regulates recruitment of RNA polymerase II (Pol-II) is a key regulatory step in determining gene expression and functional outcome, we next evaluated whether HSF induced modulation of these phenomenon in microglia in vitro. Indeed, HSF downregulated Pol-II recruitment to the promoter region of TNF-α, IL-6, NOS2, MHC-II, and transcription factor CIITA (a regulator of MHC-II expression), by itself. Moreover, HSF suppressed the lipopolysaccharide-induced increase in Pol-II recruitment as well. In addition, HSF exposure reduced the positive histone marks H3K4Me3 and H3K9/14Ac at the promoter of TNF-α, IL-6, NOS2, MHC-II, and CIITA. These studies provide a novel mechanistic insight into helminth-mediated immune suppression in microglia via modulation of epigenetic processes.

Indexed as

AnimalsAnimals, NewbornCells, CulturedCentral Nervous SystemChromatin ImmunoprecipitationCytokinesDisease Models, AnimalEpigenesis, GeneticHelminthiasisHelminthsHistocompatibility Antigens Class IIHistonesMiceMice, Inbred C57BLMicrogliaNitric Oxide Synthase Type IICytokinesHistocompatibility Antigens Class IIHistonesMHC class II transactivator proteinNitric Oxide Synthase Type IINos2 protein, mouseNuclear ProteinsPolysaccharidesRNA Polymerase IITrans-Activatorsepigeneticshelminthimmune suppressionmicroglianeurocysticercosis

Identifiers

PMID26148848
PMCPMC4552224
OpenAlexW1933555931

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.