Evidence map›Paper›PMID 26722594›Full record

ArticleInternational journal of clinical and experimental pathology2015

Effect of rTsP53 on the M1/M2 activation of bone-marrow derived macrophage in vitro.

Zhibin Chen, Fan Li, Wen Yang, Yanbing Liang, Hao Tang, Zhenyu Li, Jingguo Wu, Huaping Liang, Zhongfu Ma

Abstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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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

5 citing papers in PubMed.

  1. Review
  2. Biochemistry and biophysics reports · 2023
    Article
  3. Food and waterborne parasitology · 2022
    Article
  4. Article
  5. 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

9 authors.

Zhibin ChenDepartment of General Internal Medicine, The 1st Affiliated Hospital of Sun Yet-sen University Guangzhou 510080, Guangdong, China.
Fan LiDepartment of General Internal Medicine, The 1st Affiliated Hospital of Sun Yet-sen University Guangzhou 510080, Guangdong, China.
Wen YangDepartment of General Internal Medicine, The 1st Affiliated Hospital of Sun Yet-sen University Guangzhou 510080, Guangdong, China.
Yanbing LiangDepartment of General Internal Medicine, The 1st Affiliated Hospital of Sun Yet-sen University Guangzhou 510080, Guangdong, China.
Hao TangDepartment of General Internal Medicine, The 1st Affiliated Hospital of Sun Yet-sen University Guangzhou 510080, Guangdong, China.
Zhenyu LiDepartment of General Internal Medicine, The 1st Affiliated Hospital of Sun Yet-sen University Guangzhou 510080, Guangdong, China.
Jingguo WuDepartment of General Internal Medicine, The 1st Affiliated Hospital of Sun Yet-sen University Guangzhou 510080, Guangdong, China.
Huaping LiangThe 3rd Military Medical University Chongqing 400038, China.
Zhongfu MaDepartment of General Internal Medicine, The 1st Affiliated Hospital of Sun Yet-sen University Guangzhou 510080, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We investigated that if rTsP53 could be used to activate bone-marrow derived macrophage (BMDM) into M2 macrophage and stop M1 macrophage activation. After 72 h incubation in blank culture medium, cells with PE-CCR7 (-) and FITC-CD206 (-) was extracted and its mean proportion was 92.30 ± 0.22%. With the stimulation of 20 μg/ml IFN-γ for 72 h, cells with PE-CCR7 (+) was extracted and its mean proportion was 16.24 ± 0.82%. With the stimulation of IL-3/IL-14 (both 10 μg/ml) for 72 h, cells with FICT-CD206 (+) was extracted and its mean proportion was 87.32 ± 4.29%. Co-incubation with different dose of rTsP53 (0.001 μg/ml, 0.01 μg/ml, 0.1 μg/ml, 1 μg/ml, 2 μg/ml, 5 μg/ml, 10 μg/ml, respectively) for 72 h, FITC-CD206 (+) macrophage was extracted. The mean proportion in each group was 1.09 ± 0.22%, 2.13 ± 0.13%, 4.91 ± 0.07%, 5.48 ± 0.29%, 9.81 ± 0.06%, 12.83 ± 0.55%, 17.87 ± 0.02%, respectively. The dose of rTsP53 was significantly positive correlated to the proportion of FITC-CD206 (+) macrophage. Co-incubation with 20 μg/ml IFN-γ and 5 μg/ml rTsP53 for 72 h, cells with PE-CCR7 (+) was extracted and its mean proportion was 10.60 ± 0.19%. Compared to that of mere co-incubation with IFN-γ, there was significant difference between the two groups. ELISA showed that Th1 cytokines' (IFN-γ, IL-6 and TNF-α) level decreased in the culture medium supernatant of BMDM co-incubated with rTsP53. There was negative correlation between the Th1 cytokines' level and the dose of rTsP53. Both Th2 cytokines (IL-4 and IL-13) and regulatory cytokines in the culture medium increased. There was positive correlation between the Th2 cytokines' level and the dose of rTsP53. There was also positive correlation between the regulatory cytokines' level and the dose of rTsP53. Compared to that of BMDM co-incubated with IFN-γ, levels of TNF-α and IL-6 were significant lower than that of BMDM co-incubated with both IFN-γ and rTsP53 (both P < 0.05), while the levels of IL-4 and TGF-β were significant higher (both P < 0.05). There was no significant difference in the levels of IL-13 and IL-10 between the two groups.

Indexed as

AnimalsBacterial ProteinsBone MarrowCell LineCytokinesMacrophage ActivationMacrophagesMiceRecombinant ProteinsTrichinella spiralisBacterial ProteinsCytokinesRecombinant Proteinsbone-marrow derived macrophageM1/M2rTsP53

Identifiers

PMID26722594
PMCPMC4680539

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Registered trials

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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.