Evidence map›Paper›PMID 29722109›Full record

ArticleThe Journal of eukaryotic microbiology2018

Toxoplasma gondii Histone 4 Affects Some Functions of Murine Ana-1 Macrophages In Vitro.

Xinchao Liu, Xiaoyu Li, Qiangqiang Wang, Xiaoni Sun, Mingmin Lu, Muhammad Ehsan, Lixin Xu, RuoFeng Yan, XiaoKai Song, XiangRui Li

Abstract read
In one paragraph

Article in The Journal of eukaryotic microbiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. RecombinantVaccines · 2021
    Article
  2. Modulation Effects ofVaccines · 2020
    Article
  3. 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

10 authors.

Xinchao LiuCollege of Veterinary Medicine, Nanjing Agricultural University, Nanjing, 210095, China.
Xiaoyu LiCollege of Veterinary Medicine, Nanjing Agricultural University, Nanjing, 210095, China.
Qiangqiang WangCollege of Veterinary Medicine, Nanjing Agricultural University, Nanjing, 210095, China.
Xiaoni SunCollege of Veterinary Medicine, Nanjing Agricultural University, Nanjing, 210095, China.
Mingmin LuCollege of Veterinary Medicine, Nanjing Agricultural University, Nanjing, 210095, China.
Muhammad EhsanCollege of Veterinary Medicine, Nanjing Agricultural University, Nanjing, 210095, China.
Lixin XuCollege of Veterinary Medicine, Nanjing Agricultural University, Nanjing, 210095, China.
RuoFeng YanCollege of Veterinary Medicine, Nanjing Agricultural University, Nanjing, 210095, China.
XiaoKai SongCollege of Veterinary Medicine, Nanjing Agricultural University, Nanjing, 210095, China.
XiangRui LiCollege of Veterinary Medicine, Nanjing Agricultural University, Nanjing, 210095, China.ORCID 0000-0002-7143-6827

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toxoplasma gondii (T. gondii) is an obligate intracellular protozoan that can infect almost all nucleated cells. Histone proteins and DNA form the nucleosomes, which are the fundamental building blocks of eukaryotic chromatin. Histone 4 is an essential component of a histone octamer. In the present study, T. gondii histone 4 (TgH4) was cloned and the regulatory effect of TgH4 on murine macrophages was characterized. Bioinformatics analysis revealed that TgH4 was highly conserved in structure. Recombinant TgH4 (rTgH4) protein was identified by sera from rats experimentally infected with T. gondii and native TgH4 in the total soluble protein of T. gondii tachyzoites was recognized by polyclonal antibodies against rTgH4, as indicated by immunoblotting analysis. Immunofluorescence assay showed that TgH4 binds to macrophages. Following incubation with rTgH4, the toll-like receptor 4 (TLR4) level of the macrophages was downregulated. Meanwhile, chemotaxis and the proliferation of macrophages were inhibited. However, rTgH4 can promote phagocytosis, apoptosis, and the secretion of nitric oxide, interleukin-6, and tumor necrosis factor-α from macrophages. Just 80 μg/ml rTgH4 can significantly elevate the secretion of interleukin-10 and interleukin-1β (p < 0.05 and p < 0.01). Viewed together, these outcomes indicated that rTgH4 can affect the functions of murine macrophages in vitro.

Indexed as

Amino Acid SequenceAnimalsAntibodies, ProtozoanAntigens, ProtozoanApoptosisCell Cycle ProteinsCytokinesDown-RegulationFemaleImmunodominant EpitopesInterleukin-10Interleukin-1betaInterleukin-6MacrophagesMiceNitric OxideAntibodies, ProtozoanAntigens, ProtozoanBtg3 protein, mouseCell Cycle ProteinsCytokinesH4 protein, Toxoplasma gondiiImmunodominant EpitopesInterleukin-10Interleukin-1betaInterleukin-6Nitric OxideProteinsProtozoan ProteinsRecombinant ProteinsTlr4 protein, mouseToll-Like Receptor 4Tumor Necrosis Factor-alpha

Identifiers

PMID29722109
PMCPMC6282536

What OpenQuestion holds

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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.