Evidence map›Paper›PMID 36474240›Full record

ArticleParasites & vectors2022

Activation of primary hepatic stellate cells and liver fibrosis induced by targeting TGF-β1/Smad signaling in schistosomiasis in mice.

Ping Huang, Huihui Ma, Yun Cao, Tingzheng Zhan, Tingting Zhang, Xinyi Wang, Yanan Zhang, Jing Xu, Chaoming Xia

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

13 citing papers in PubMed, 30 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Ping Huang *Department of Pathogen Biology, Suzhou Medical College of Soochow University, 199 Renai Road, Suzhou, 215123, Jiangsu, China.
Huihui Ma *Department of Pathogen Biology, Suzhou Medical College of Soochow University, 199 Renai Road, Suzhou, 215123, Jiangsu, China.
Yun Cao *Department of Pathogen Biology, Suzhou Medical College of Soochow University, 199 Renai Road, Suzhou, 215123, Jiangsu, China.
Tingzheng ZhanDepartment of Pathogen Biology, Suzhou Medical College of Soochow University, 199 Renai Road, Suzhou, 215123, Jiangsu, China.
Tingting ZhangDepartment of Pathogen Biology, Suzhou Medical College of Soochow University, 199 Renai Road, Suzhou, 215123, Jiangsu, China.
Xinyi WangDepartment of Pathogen Biology, Suzhou Medical College of Soochow University, 199 Renai Road, Suzhou, 215123, Jiangsu, China.
Yanan ZhangDepartment of Pathogen Biology, Suzhou Medical College of Soochow University, 199 Renai Road, Suzhou, 215123, Jiangsu, China.
Jing XuDepartment of Pathogen Biology, Suzhou Medical College of Soochow University, 199 Renai Road, Suzhou, 215123, Jiangsu, China.
Chaoming XiaDepartment of Pathogen Biology, Suzhou Medical College of Soochow University, 199 Renai Road, Suzhou, 215123, Jiangsu, China. xiachaoming@suda.edu.cn.
Soochow University · CNBengbu Medical College · CNGuangxi Medical University · CN

Funding

China Postdoctoral Science Foundation 2022M712307Hainan Provincial Natural Science Foundation of China 821RC1068Jiangsu Funding Program for Excellent Postdoctoral Talent 2022ZB573National Natural Science Foundation of China 82172294Priority Academic Program Development of Jiangsu Higher Education Institutions YX13400214
6 · The paper itself

Abstract

backgroundIn mice, liver fibrosis is the most serious pathologic change during Schistosoma japonicum (S. japonicum) infection. Schistosomiasis is mainly characterized by schistosome egg-induced granulomatous fibrosis. Hepatic stellate cells (HSCs) are mainly responsible for the net accumulation of collagens and fibrosis formation in the liver. Activated HSCs regulated by transforming growth factor-β1 (TGF-β1)/Smad signaling have emerged as the critical regulatory pathway in hepatitis virus or carbon tetrachloride-induced liver fibrosis. However, the detailed mechanism of HSC activation in schistosome-induced liver fibrosis is poorly understood.

methodsSchistosoma japonicum-induced murine models and a control group were generated by abdominal infection with 15 (± 1) cercariae. The purity of cultured primary HSCs was evaluated by immunocytochemistry. The histopathological changes in the livers of infected mice were estimated by hematoxylin-eosin and Masson staining. Dynamic expression of pro-fibrotic molecules and microRNAs was detected by real-time quantitative PCR (RT-qPCR). Mainly members involved in the TGF-β1/Smad signaling pathway were examined via RT-qPCR and Western blot.

resultsThe egg-induced granulomatous inflammation formed at 4 weeks post-infection (wpi) and developed progressively. Alpha-smooth muscle actin (α-SMA), collagen I, collagen III, TGF-β1, Smad2, Smad3, and Smad4 showed a significant increase in mitochondrial RNA (mRNA) and protein expression compared with the control group at 7 and 9 weeks post-infection (wpi), while an opposite effect on Smad7 was observed. In addition, the mRNA expression of microRNA-21 (miRNA-21) was significantly increased at 7 wpi, and the mRNA expression of miRNA-454 was decreased starting from 4 wpi.

conclusionOur present findings revealed that HSCs regulated by the TGF-β1/Smad signaling pathway play an important role in liver fibrosis in S. japonicum-infected mice, which may provide proof of concept for liver fibrosis in schistosomiasis.

Indexed as

Hepatic Stellate CellsMicroRNAsAnimalsFibrosisLiver CirrhosisMiceRNA, MessengerSignal TransductionTransforming Growth Factor beta1MicroRNAsRNA, MessengerTransforming Growth Factor beta1Hepatic stellate cellsLiver fibrosisMicroRNAsSchistosomiasisTGF-β1/Smad signaling

Identifiers

PMID36474240
PMCPMC9727849
OpenAlexW4311588907

What OpenQuestion holds

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LicenceCC BY
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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.