Evidence map›Paper›PMID 29436649›Full record

ArticleMolecular medicine reports2018

Interleukin‑10 promotes primary rat hepatic stellate cell senescence by upregulating the expression levels of p53 and p21.

Yue-Hong Huang, Ming-Hua Chen, Qi-Lan Guo, Yun-Xin Chen, Li-Juan Zhang, Zhi-Xin Chen, Xiao-Zhong Wang

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

15 citing papers in PubMed, 33 citations in OpenAlex.

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  7. [Reversal mechanism of hepatic fibrosis].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2022
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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

7 authors at 2 institutions in 1 country.

Yue-Hong HuangDepartment of Gastroenterology, Fujian Medical University Union Hospital, Fuzhou, Fujian 350001, P.R. China.
Ming-Hua ChenDepartment of Gastroenterology, Fujian Medical University Union Hospital, Fuzhou, Fujian 350001, P.R. China.
Qi-Lan GuoDepartment of Gastroenterology, Fujian Medical University Union Hospital, Fuzhou, Fujian 350001, P.R. China.
Yun-Xin ChenDepartment of Gastroenterology, Fujian Medical University Union Hospital, Fuzhou, Fujian 350001, P.R. China.
Li-Juan ZhangDepartment of Gastroenterology, Fujian Medical University Union Hospital, Fuzhou, Fujian 350001, P.R. China.
Zhi-Xin ChenDepartment of Gastroenterology, Fujian Medical University Union Hospital, Fuzhou, Fujian 350001, P.R. China.
Xiao-Zhong WangDepartment of Gastroenterology, Fujian Medical University Union Hospital, Fuzhou, Fujian 350001, P.R. China.
Fujian Medical University · CNUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver fibrosis is characterized by the excessive deposition of extracellular matrix (ECM) components, and activated hepatic stellate cells (HSCs) are a primary source of ECM. Several studies have revealed that the induction of HSC senescence may reduce liver fibrosis. The effect of interleukin‑10 (IL‑10) on the senescence of activated HSCs is not fully understood. Therefore, the present study examined its effects and potential mechanisms in activated primary rat HSCs. Collagenase perfusion and density gradient centrifugation methods were used to isolate rat HSCs. HSCs were identified by autofluorescence, Oil Red O staining and immunocytochemical analysis. Activated HSCs were treated with 0, 10, 20 or 40 ng/ml IL‑10 for 24 h. Senescence‑associated β‑galactosidase (SA‑β‑Gal) staining, flow cytometry analysis and a cell counting kit‑8 assay were performed to detect the senescence, apoptosis and viability of rat HSCs, respectively. Reverse transcription‑quantitative polymerase chain reaction, western blot analysis and enzyme linked immunosorbent assays were used to detect the expression of senescence‑associated proteins and cytokines. Freshly isolated rat HSCs exhibited a striking blue‑green autofluorescence and HSC retinoid droplets were stained bright red by Oil Red O. Immunocytochemical analysis demonstrated the cytoplasmic expression of HSC markers desmin and α‑smooth muscle actin. The number of SA‑β‑Gal positive HSCs, the apoptotic rate and the expression levels of p53, p21 and tumor necrosis factor‑α were significantly increased following IL‑10 treatment. HSC viability and IL‑6 and IL‑8 expression levels were significantly decreased compared with the control group. In summary, primary rat HSCs were successfully isolated and IL‑10 was demonstrated to promote the senescence of activated primary rat HSCs through the upregulation of p53 and p21 expression.

Indexed as

AnimalsApoptosisCell ProliferationCellular SenescenceCytokinesGene Expression RegulationHepatic Stellate CellsInflammation MediatorsInterleukin-10MaleProto-Oncogene Proteins p21(ras)RatsSignal TransductionTumor Suppressor Protein p53CytokinesInflammation MediatorsInterleukin-10Proto-Oncogene Proteins p21(ras)Tumor Suppressor Protein p53cytokinehepatic stellate cellsinterleukin-10p21p53senescence

Identifiers

PMID29436649
PMCPMC5866012
OpenAlexW2793448621

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.