Evidence map›Paper›PMID 31665090›Full record

ArticleStem cell research & therapy2019

Radio-detoxified LPS alters bone marrow-derived extracellular vesicles and endothelial progenitor cells.

Hargita Hegyesi, Nikolett Sándor, Géza Sáfrány, Virág Lovas, Árpád Kovács, Angéla Takács, László Kőhidai, Lilla Turiák, Ágnes Kittel, Krisztina Pálóczi and 2 more

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

5 citing papers in PubMed, 11 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

12 authors at 4 institutions in 1 country.

Hargita HegyesiDepartment of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary. hegyesi.hargita@med.semmelweis-univ.hu.ORCID 0000-0002-8800-5169
Nikolett SándorNational Research Directorate for Radiobiology and Radiohygiene, National Public Health Center, Budapest, Hungary.
Géza SáfrányNational Research Directorate for Radiobiology and Radiohygiene, National Public Health Center, Budapest, Hungary.
Virág LovasDepartment of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
Árpád KovácsDepartment of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
Angéla TakácsDepartment of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
László KőhidaiDepartment of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
Lilla TuriákMS Proteomics Research Group, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary.
Ágnes KittelInstitute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.
Krisztina PálócziDepartment of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
Lóránd BertókNational Research Directorate for Radiobiology and Radiohygiene, National Public Health Center, Budapest, Hungary.
Edit Irén BuzásDepartment of Genetics, Cell- and Immunobiology, Semmelweis University, Budapest, Hungary.
Semmelweis University · HUFrédéric Joliot-Curie National Research Institute for Radiobiology and Radiohygiene · HUHungarian Academy of Sciences · HUHUN-REN Institute of Experimental Medicine · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stem cell-based therapies raise hope for cell replacement and provide opportunity for cardiac regenerative medicine and tumor therapy. Extracellular vesicles are a membrane-enclosed intercellular delivery system with the potential to improve the therapeutic efficacy of the treatment of a variety of disorders. As the incidence of breast cancer continues to rise, radiotherapy has emerged as a leading treatment modality. Radiotherapy also increases the risk of coronary heart disease and cardiac mortality. In a chest-irradiated mouse model of cardiac injury, we investigated the effects of local irradiation. We found an increased lethality after 16 Gy irradiation. Importantly, radio-detoxified LPS (RD-LPS) treatment prolonged the survival significantly. By flow cytometry, we demonstrated that upon administration of RD-LPS, the number of bone marrow-derived endothelial progenitor cells increased in the bone marrow and, in particular, in the circulation. Furthermore, mass spectrometry analysis showed that RD-LPS altered the proteomic composition of bone marrow cell-derived small extracellular vesicles (sEVs). RD-LPS treatment increased interferon-induced transmembrane protein-3 (IFITM3) expression markedly both in bone marrow cells and in bone marrow cell-derived small extracellular vesicles. This is the first study to demonstrate that radio-detoxified LPS treatment induces an increase of circulating endothelial progenitor cells (EPCs) in parallel with a reduced radiotherapy-related mortality. While the total number of bone marrow-derived extracellular vesicles was significantly increased 24 h after treatment in the RD-LPS groups, the number of endothelial progenitor cells was reduced in animals injected with GW4896 (a chemical inhibitor of exosome biogenesis) as compared with controls. In contrast to these in vivo results, in vitro experiments did not support the effect of sEVs on EPCs. Our data raise the intriguing possibility that IFITM3 may serve as a marker of the radio-detoxified LPS treatment.

Indexed as

Gamma RaysAnimalsBone Marrow CellsCell MovementCell SurvivalEndothelial Progenitor CellsExtracellular VesiclesGene SilencingLipopolysaccharidesMembrane ProteinsMice, Inbred C57BLRadiation-Protective Agentsfragilis protein, mouseLipopolysaccharidesMembrane ProteinsRadiation-Protective AgentsBone marrowEndothelial progenitor cellExosomesExtracellular vesiclesIFITM3Radio-detoxified endotoxin

Identifiers

PMID31665090
PMCPMC6819448
OpenAlexW2982643102

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Registered trials

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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.