Evidence map›Paper›PMID 28193696›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2017

Astrocytic Orosomucoid-2 Modulates Microglial Activation and Neuroinflammation.

Myungjin Jo, Jong-Heon Kim, Gyun Jee Song, Minchul Seo, Eun Mi Hwang, Kyoungho Suk

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 109 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
109citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 4% 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

109 citing papers in PubMed, 1 synthesis or guideline pooled it, 177 citations in OpenAlex.

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49 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Myungjin JoDepartment of Pharmacology, Brain Science and Engineering Institute, Biomedical Convergence Program for Creative Talent, Kyungpook National University School of Medicine, Daegu 41944, Republic of Korea, and.
Jong-Heon KimDepartment of Pharmacology, Brain Science and Engineering Institute, Biomedical Convergence Program for Creative Talent, Kyungpook National University School of Medicine, Daegu 41944, Republic of Korea, and.
Gyun Jee SongDepartment of Pharmacology, Brain Science and Engineering Institute, Biomedical Convergence Program for Creative Talent, Kyungpook National University School of Medicine, Daegu 41944, Republic of Korea, and.
Minchul SeoDepartment of Pharmacology, Brain Science and Engineering Institute, Biomedical Convergence Program for Creative Talent, Kyungpook National University School of Medicine, Daegu 41944, Republic of Korea, and.
Eun Mi HwangCenter for Functional Connectomics, Korea Institute of Science and Technology, Seoul 02792, Republic of Korea.ORCID 0000-0002-3130-8572
Kyoungho SukDepartment of Pharmacology, Brain Science and Engineering Institute, Biomedical Convergence Program for Creative Talent, Kyungpook National University School of Medicine, Daegu 41944, Republic of Korea, and ksuk@knu.ac.kr.ORCID 0000-0002-9555-4203
Kyungpook National University · KRKorea Institute of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Orosomucoid (ORM) is an acute-phase protein that belongs to the immunocalin subfamily, a group of small-molecule-binding proteins with immunomodulatory functions. Little is known about the role of ORM proteins in the CNS. The aim of the present study was to investigate the brain expression of ORM and its role in neuroinflammation. Expression of Orm2, but not Orm1 or Orm3, was highly induced in the mouse brain after systemic injection of lipopolysaccharide (LPS). Plasma levels of ORM2 were also significantly higher in patients with cognitive impairment than in normal subjects. RT-PCR, Western blot, and immunofluorescence analyses revealed that astrocytes are the major cellular sources of ORM2 in the inflamed mouse brain. Recombinant ORM2 protein treatment decreased microglial production of proinflammatory mediators and reduced microglia-mediated neurotoxicity

Indexed as

AnimalsBrainCytokinesEncephalitisHumansImmunologic FactorsMaleMiceMice, Inbred C57BLMicrogliaOrosomucoidCytokinesImmunologic FactorsORM2 protein, humanOrosomucoidastrocyteCCR5microgliamigrationneuroinflammationOrm2

Identifiers

PMID28193696
PMCPMC6596722
OpenAlexW2588926033

What OpenQuestion holds

Textmetadata
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.