Evidence map›Paper›PMID 36949464›Full record

ArticleStem cell research & therapy2023

Superior protective effects of PGE2 priming mesenchymal stem cells against LPS-induced acute lung injury (ALI) through macrophage immunomodulation.

Kamal Hezam, Chen Wang, Enze Fu, Manqian Zhou, Yue Liu, Hui Wang, Lihong Zhu, Zhibo Han, Zhong-Chao Han, Ying Chang and 1 more

Open access · goldFull text read
In one paragraph

Article in Stem cell research & therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
13.2field-weighted citation impact, top 1% 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

33 citing papers in PubMed, 46 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

11 authors at 3 institutions in 1 country.

Kamal Hezam *Nankai University School of Medicine, Tianjin, 300071, China.
Chen Wang *Nankai University School of Medicine, Tianjin, 300071, China.
Enze FuNankai University School of Medicine, Tianjin, 300071, China.
Manqian ZhouDepartment of Radiation Oncology, Tianjin Union Medical Center, Nankai University, Tianjin, 300120, China.
Yue LiuNankai University School of Medicine, Tianjin, 300071, China.
Hui WangDepartment of Radiation Oncology, Tianjin Union Medical Center, Nankai University, Tianjin, 300120, China.
Lihong ZhuDepartment of Gynecologic Oncology, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, 100026, China.
Zhibo HanJiangxi Engineering Research Center for Stem Cells, Shangrao, 334109, Jiangxi, China.
Zhong-Chao HanJiangxi Engineering Research Center for Stem Cells, Shangrao, 334109, Jiangxi, China.
Ying ChangTianjin Key Laboratory of Human Development and Reproductive Regulation, Tianjin Central Hospital of Gynecology Obstetrics, Nankai University Affiliated Hospital of Obstetrics and Gynecology, Tianjin, 300052, China. changying4470@126.com.
Zongjin LiNankai University School of Medicine, Tianjin, 300071, China. zongjinli@nankai.edu.cn.ORCID 0000-0002-4603-3743
Nankai University · CNSinovac Biotech · CNCapital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMesenchymal stem cells (MSCs) have demonstrated remarkable therapeutic promise for acute lung injury (ALI) and its severe form, acute respiratory distress syndrome (ARDS). MSC secretomes contain various immunoregulatory mediators that modulate both innate and adaptive immune responses. Priming MSCs has been widely considered to boost their therapeutic efficacy for a variety of diseases. Prostaglandin E2 (PGE2) plays a vital role in physiological processes that mediate the regeneration of injured organs.

methodsThis work utilized PGE2 to prime MSCs and investigated their therapeutic potential in ALI models. MSCs were obtained from human placental tissue. MSCs were transduced with firefly luciferase (Fluc)/eGFP fusion protein for real-time monitoring of MSC migration. Comprehensive genomic analyses explored the therapeutic effects and molecular mechanisms of PGE2-primed MSCs in LPS-induced ALI models.

resultsOur results demonstrated that PGE2-MSCs effectively ameliorated lung injury and decreased total cell numbers, neutrophils, macrophages, and protein levels in bronchoalveolar lavage fluid (BALF). Meanwhile, treating ALI mice with PGE2-MSCs dramatically reduced histopathological changes and proinflammatory cytokines while increasing anti-inflammatory cytokines. Furthermore, our findings supported that PGE2 priming improved the therapeutic efficacy of MSCs through M2 macrophage polarization.

conclusionPGE2-MSC therapy significantly reduced the severity of LPS-induced ALI in mice by modulating macrophage polarization and cytokine production. This strategy boosts the therapeutic efficacy of MSCs in cell-based ALI therapy.

Indexed as

Acute Lung InjuryMesenchymal Stem CellsMesenchymal Stem Cell TransplantationAnimalsCytokinesDinoprostoneFemaleHumansImmunityImmunomodulationLipopolysaccharidesLungMacrophagesMicePlacentaPregnancyCytokinesDinoprostoneLipopolysaccharidesAcute lung injury (ALI)Acute respiratory distress syndrome (ARDS)Mesenchymal stem cells (MSCs)PrimingProstaglandin E2 (PGE2)

Identifiers

PMID36949464
PMCPMC10032272
OpenAlexW4353092950

What OpenQuestion holds

Textfull text, public
LicenceCC BY
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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.