Evidence map›Paper›PMID 32270546›Full record

ArticleCell proliferation2020

Interleukin-11 regulates the fate of adipose-derived mesenchymal stem cells via STAT3 signalling pathways.

Wenlong Yang, Shuning Zhang, Tiantong Ou, Hao Jiang, Daile Jia, Zhiyong Qi, Yunzeng Zou, Juying Qian, Aijun Sun, Junbo Ge

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  6. Harnessing the regenerative potential ofbioRxiv : the preprint server for biology · 2024
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Roles and mechanism of IL-11 in vascular diseases.Frontiers in cardiovascular medicine · 2023
    Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
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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

10 authors at 1 institution in 1 country.

Wenlong YangDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai, China.ORCID https://orcid.org/0000-0002-4264-1266
Shuning ZhangDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai, China.
Tiantong OuDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai, China.
Hao JiangDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai, China.
Daile JiaDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai, China.
Zhiyong QiDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai, China.
Yunzeng ZouDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai, China.
Juying QianDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai, China.
Aijun SunDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai, China.
Junbo GeDepartment of Cardiology, Zhongshan Hospital, Fudan University, Shanghai, China.
Sun Yat-sen University · CN

Funding

Excellent Key Youth Program of Zhongshan Hospital of Fudan University 2019ZSYXGG13National Natural Science Foundation of China 81570317National Natural Science Foundation of China Innovation Research Group Science Foundation 81521001National Science Fund for Distinguished Young Scholars 81725002
6 · The paper itself

Abstract

objectiveAdipose-derived mesenchymal stem cells (ADSCs) offer great promise as cell therapy for ischaemic diseases. Due to their poor survival in the ischaemic environment, the therapeutic efficacy of ADSCs is still relatively low. Interleukin-11 (IL-11) has been shown to play a key role in promoting cell proliferation and protecting cells from oxidative stress injury. The aim of this study was to determine whether IL-11 could improve therapeutic efficacy of ADSCs in ischaemic diseases. METHODS AND

resultsADSCs were prepared from inguinal subcutaneous adipose tissue and exposed to hypoxic environment. The protein expression of IL-11 was decreased after hypoxic treatment. In addition, ADSCs viability was increased after IL-11 treatment under hypoxia. Moreover, IL-11 enhanced ADSCs viability in a dose-dependent manner under normoxia. Importantly, IL-11 promoted ADSCs proliferation and migration and protected ADSCs against hydrogen peroxide-induced cellular death. Notably, IL-11 enhanced ADSCs proliferation and migration, also promoted cell survival and apoptosis resistance by STAT3 signalling. In vivo, mice were subjected to limb ischaemia and treated with IL-11 overexpression ADSCs and control ADSCs. IL-11 overexpression ADSCs improved perfusion recovery in the ischaemic muscles.

conclusionsWe provide the evidence that IL-11 promoted ADSCs proliferation, stimulated ADSCs migration and attenuated ADSCs apoptosis by activation of STAT3 signalling. These results suggest that IL-11 facilitated ADSCs engraftment in ischaemic tissue, thereby enhanced ADSCs therapeutic efficacy.

Indexed as

Adipose TissueAnimalsApoptosisCell DifferentiationCell MovementCell ProliferationCells, CulturedCell SurvivalInterleukin-11IschemiaMesenchymal Stem CellsMiceMice, Inbred C57BLSignal TransductionSTAT3 Transcription FactorInterleukin-11Stat3 protein, mouseSTAT3 Transcription Factoradipose-derived mesenchymal stem cellscell therapyinterleukin-11limb ischaemia

Identifiers

PMID32270546
PMCPMC7260062
OpenAlexW3015367575

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.