Evidence map›Paper›PMID 37817516›Full record

ArticleCurrent stem cell research & therapy2024

Mesenchymal Stem Cell-conditioned Medium Protecting Renal Tubular Epithelial Cells by Inhibiting Hypoxia-inducible Factor-1α and Nuclear Receptor Coactivator-1.

Chunling Liao, Yiping Liu, Yongda Lin, Jiali Wang, Tianbiao Zhou, Wenjuan Weng

Abstract read
PubMed Publisher
In one paragraph

Article in Current stem cell research & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 22% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 1 institution in 1 country.

Chunling LiaoDepartment of Nephrology, the Second Affiliated Hospital of Shantou University Medical College, Shantou, 515041, China.
Yiping LiuDepartment of Nephrology, the Second Affiliated Hospital of Shantou University Medical College, Shantou, 515041, China.
Yongda LinDepartment of Nephrology, the Second Affiliated Hospital of Shantou University Medical College, Shantou, 515041, China.
Jiali WangDepartment of Nephrology, the Second Affiliated Hospital of Shantou University Medical College, Shantou, 515041, China.
Tianbiao ZhouDepartment of Nephrology, the Second Affiliated Hospital of Shantou University Medical College, Shantou, 515041, China.
Wenjuan WengDepartment of Nephrology, the Second Affiliated Hospital of Shantou University Medical College, Shantou, 515041, China.
Shantou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute kidney injury (AKI) is characterized by inflammatory infiltration and damage and death of renal tubular epithelial cells (RTECs), in which hypoxia plays an important role. Deferoxamine (DFO) is a well-accepted chemical hypoxia-mimetic agent. Mesenchymal stem cell-conditioned medium (MSC-CM) can reduce local inflammation and repair tissue. In this study, we explored the effect and molecular mechanism of MSC-CM-mediated protection of RTECs under DFO-induced hypoxia.

methodsRat renal proximal tubule NRK-52E cells were treated with different concentrations of DFO for 24 hours, followed by evaluation of RTEC injury, using a Cell Counting Kit-8 (CCK-8) to detect cell viability and western blotting to evaluate the expression of transforming growth factor- beta 1 (TGF-β1), α-smooth muscle actin (α-SMA), and hypoxia-inducible factor-1 alpha (HIF-1α) in NRK-52E cells. Then, three groups of NRK-52E cells were used in experiments, including normal control (NC), 25 μM DFO, and 25 μM DFO + MSC-CM. MSC-CM was obtained from the human umbilical cord. MSC-CM was used to culture cells for 12 hours before DFO treatment, then fresh MSC-CM and 25 μM DFO were added, and cells were cultured for another 24 hours before analysis.

resultsWestern blotting and cellular immunofluorescence staining showed culture of NRK-52E cells in 25 μM DFO for 24 hours induced HIF-1α and nuclear receptor coactivator-1 (NCoA-1), simulating hypoxia. MSC-CM could inhibit the DFO-induced up-regulation of α-SMA, TGF-β1, HIF-1α and NCoA-1.

conclusionOur results suggest that MSC-CM has a protective effect on RTECs by down-regulating HIF-1α and NCoA-1, which may be the harmful factors in renal injury.

Indexed as

Epithelial CellsHypoxia-Inducible Factor 1, alpha SubunitMesenchymal Stem CellsAcute Kidney InjuryAnimalsCell HypoxiaCell LineCell SurvivalCulture Media, ConditionedDeferoxamineHumansKidney TubulesKidney Tubules, ProximalNuclear Receptor Coactivator 1RatsTransforming Growth Factor beta1Culture Media, ConditionedDeferoxamineHif1a protein, ratHypoxia-Inducible Factor 1, alpha SubunitNcoa1 protein, ratNuclear Receptor Coactivator 1Transforming Growth Factor beta1Acute kidney injury (AKI)deferoxamine (DFO)HIF-1αMSC-conditioned medium (MSC-CM)NCoA-1.renal tubular epithelial cells (RTECs)

Identifiers

PMID37817516
OpenAlexW4387456768

What OpenQuestion holds

Textmetadata
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.