Evidence map›Paper›PMID 28458256›Full record

ArticleAging2017

Aging-associated oxidative stress inhibits liver progenitor cell activation in mice.

Yiji Cheng, Xue Wang, Bei Wang, Hong Zhou, Shipeng Dang, Yufang Shi, Li Hao, Qingquan Luo, Min Jin, Qianjun Zhou and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Aging, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

23 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Stem cell-based therapeutic strategies for liver aging.Liver research (Beijing, China) · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Overview of Innate Immune Cell Landscape in Liver Aging.International journal of molecular sciences · 2023
    Review
  10. Article
  11. Review
  12. Article
  13. Cell Sources and Influencing Factors of Liver Regeneration: A Review.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Review
  14. Article
  15. The Role of Autophagy for the Regeneration of the Aging Liver.International journal of molecular sciences · 2020
    Review
  16. Article
  17. Hallmarks of Aging in the Liver.Computational and structural biotechnology journal · 2019
    Review
  18. Review
  19. Article
  20. 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

11 authors at 4 institutions in 1 country.

Yiji ChengShanghai Institute of Immunology and Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Xue WangShanghai Institute of Immunology and Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Bei WangKey Laboratory of Stem Cell Biology, Institute of Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences and Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Hong ZhouKey Laboratory of Stem Cell Biology, Institute of Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences and Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Shipeng DangKey Laboratory of Stem Cell Biology, Institute of Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences and Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yufang ShiKey Laboratory of Stem Cell Biology, Institute of Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences and Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Li HaoClinical Laboratory, The First Affiliated Hospital of Anhui Medical University, Hefei, China.
Qingquan LuoShanghai Institute of Immunology and Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Min JinKey Laboratory of Stem Cell Biology, Institute of Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences and Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Qianjun ZhouShanghai Institute of Immunology and Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yanyun ZhangShanghai Institute of Immunology and Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Shanghai Jiao Tong University · CNShanghai Chest Hospital · CNFirst Affiliated Hospital of Anhui Medical University · CNShanghai Institutes for Biological Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have discovered aging-associated changes of adult stem cells in various tissues and organs, which potentially contribute to the organismal aging. However, aging-associated changes of liver progenitor cells (LPCs) remain elusive. Employing young (2-month-old) and old (24-month-old) mice, we found diverse novel alterations in LPC activation during aging. LPCs in young mice could be activated and proliferate upon liver injury, whereas the counterparts in old mice failed to respond and proliferate, leading to the impaired liver regeneration. Surprisingly, isolated LPCs from young and old mice did not exhibit significant difference in their clonogenic and proliferative capacity. Later, we uncovered that the decreased activation and proliferation of LPCs were due to excessive reactive oxygen species produced by neutrophils infiltrated into niche, which was resulted from chemokine production from activated hepatic stellate cells during aging. This study demonstrates aging-associated changes in LPC activation and reveals critical roles for the stem cell niche, including neutrophils and hepatic stellate cells, in the negative regulation of LPCs during aging.

Indexed as

Cell ProliferationLiver RegenerationOxidative StressAge FactorsAgingAnimalsCells, CulturedChemokines, CXCHepatic Stellate CellsLiverMice, Inbred C57BLNeutrophil InfiltrationNeutrophilsParacrine CommunicationPhenotypeReactive Oxygen SpeciesChemokines, CXCCxcl7 protein, mouseReactive Oxygen Speciesagingliver regenerationneutrophilreactive oxygen speciesstem cells

Identifiers

PMID28458256
PMCPMC5472737
OpenAlexW2608238429

What OpenQuestion 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 OpenQuestion graph.