Evidence map›Paper›PMID 35987696›Full record

ArticleStem cell research & therapy2022

Protective effect of adipose-derived stromal cell-secretome attenuate autophagy induced by liver ischemia-reperfusion and partial hepatectomy.

Yajun Ma, Zhihui Jiao, Xiaoning Liu, Qianzhen Zhang, Chenxi Piao, Jiayuan Xu, Hongbin Wang

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

12 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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  4. European journal of translational myology · 2026
    Article
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  8. Review
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  12. The paradigm of stem cell secretome in tissue repair and regeneration: Present and future perspectives.Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society
    Review
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 1 institution in 1 country.

Yajun MaCollege of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, People's Republic of China.
Zhihui JiaoCollege of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, People's Republic of China.
Xiaoning LiuCollege of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, People's Republic of China.
Qianzhen ZhangCollege of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, People's Republic of China.
Chenxi PiaoCollege of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, People's Republic of China.
Jiayuan XuCollege of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, People's Republic of China.
Hongbin WangCollege of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, People's Republic of China. hbwang1940@neau.edu.cn.ORCID 0000-0002-4454-3328
Northeast Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe therapeutic effects of adipose-derived mesenchymal stromal cells (ADSCs) may be mainly mediated by their paracrine effects. The ADSC-secretome can ameliorate hepatic ischemia-reperfusion injury (IRI). We explored the therapeutic effect of the ADSC-secretome from the perspective of excessive hepatocyte autophagy induced by hepatic IRI.

methodsWe established a miniature pig model of hepatic ischemia-reperfusion (I/R) and hepatectomy using a laparoscopic technique and transplanted ADSCs and the ADSC-secretome into the liver parenchyma immediately after surgery. Liver injury and hepatocyte autophagy were evaluated by histopathological examination and assessment of relevant cytokines and other factors.

resultsThe results showed that the ADSC-secretome alleviated the pathological changes of liver tissue and the microstructural damage of hepatocytes after IRI. Moreover, the expression levels of autophagy-related markers including Beclin-1, ATG5, ATG12, and LC3II/LC3I decreased, whereas those of p62 increased during phagophore expansion. Furthermore, the expression levels of markers related to the autophagy inhibition pathway phosphatidylinositol-3-kinase/Akt/mammalian target of rapamycin (PI3K/Akt/mTOR), including PI3K, Akt, and mTOR, increased.

conclusionThe ADSC-secretome attenuates hepatic I/R and hepatectomy-induced liver damage by inhibiting autophagy, which is possibly mediated by activation of the PI3K/Akt/mTOR signaling pathway. In addition, there was no significant difference between ADSCs and the ADSC-secretome in the regulation of hepatocyte autophagy. Therefore, ADSCs may improve the excessive autophagy-induced injury of hepatocytes in hepatic I/R and hepatectomy through paracrine effect. Our findings provide new insight into the therapeutic potential of cell-free products, which could replace cell therapy in liver diseases.

Indexed as

Liver DiseasesMesenchymal Stem CellsReperfusion InjuryAnimalsAutophagyHepatectomyIschemiaLiverMammalsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReperfusionSecretomeSwineTOR Serine-Threonine KinasesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesADSC-secretomeAutophagyIRILaparoscopyMiniature pig

Identifiers

PMID35987696
PMCPMC9392224
OpenAlexW4292824627

What Socratic holds

Textmetadata
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 Socratic graph.