Evidence map›Paper›PMID 31355328›Full record

ArticleScience advances2019

Extracellular vesicles derived from ODN-stimulated macrophages transfer and activate Cdc42 in recipient cells and thereby increase cellular permissiveness to EV uptake.

Ying Zhang, Xue Jin, Jiaqi Liang, Yilan Guo, Gaoge Sun, Xianfeng Zeng, Hang Yin

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

27 citing papers in PubMed, 43 citations in OpenAlex.

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  17. Review
  18. Comparative Proteomic Analysis of Membrane Vesicles from ClinicalClinical, cosmetic and investigational dermatology · 2022
    Article
  19. Summary of Prof. Yin's CSEMV-EVCNA award lecture 2021.Extracellular vesicles and circulating nucleic acids · 2022
    Article
  20. Mesenchymal Stem Cell Senescence and Osteogenesis.Medicina (Kaunas, Lithuania) · 2021
    Review
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

7 authors at 2 institutions in 1 country.

Ying ZhangSchool of Pharmaceutical Sciences, Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Tsinghua University, Beijing 100082, China.ORCID 0000-0003-3362-3952
Xue JinTsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing 100084, China.ORCID 0000-0003-4214-6238
Jiaqi LiangTsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing 100084, China.ORCID 0000-0002-6777-6263
Yilan GuoTsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing 100084, China.ORCID 0000-0001-9058-0165
Gaoge SunTsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing 100084, China.ORCID 0000-0002-7656-1125
Xianfeng ZengTsinghua University-Peking University Joint Center for Life Sciences, Tsinghua University, Beijing 100084, China.ORCID 0000-0001-9593-3388
Hang YinSchool of Pharmaceutical Sciences, Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Tsinghua University, Beijing 100082, China.ORCID 0000-0002-9762-4818
Peking University · CNCenter for Life Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endosomal Toll-like receptors (TLRs) mediate intracellular innate immunity via the recognition of DNA and RNA sequences. Recent work has reported a role for extracellular vesicles (EVs), known to transfer various nucleic acids, in uptake of TLR-activating molecules, raising speculation about possible roles of EVs in innate immune surveillance. Whether EV-mediated uptake is a general mechanism, however, was unresolved; and the molecular machinery that might be involved was unknown. We show that, when macrophages are stimulated with the TLR9 agonist CpG oligodeoxynucleotides (ODN), the secreted EVs transport ODN into naïve macrophages and induce the release of chemokine TNF-α. In addition, these EVs transfer Cdc42 into recipient cells, resulting in further enhancement of their cellular uptake. Transport of ODN and Cdc42 from TLR9-activated macrophages to naïve cells via EVs exerts synergetic effects in propagation of the intracellular immune response, suggesting a general mechanism of EV-mediated uptake of pathogen-associated molecular patterns.

Indexed as

cdc42 GTP-Binding ProteinCell LineDNAEndosomesExtracellular VesiclesGene Expression RegulationHumansImmunity, CellularMacrophagesNanoparticlesOligodeoxyribonucleotidesProteomicsRNAToll-Like Receptor 9Tumor Necrosis Factor-alphacdc42 GTP-Binding ProteinCDC42 protein, humanCPG-oligonucleotideDNAOligodeoxyribonucleotidesRNATLR9 protein, humanToll-Like Receptor 9Tumor Necrosis Factor-alpha

Identifiers

PMID31355328
PMCPMC6656539
OpenAlexW2964136915

What OpenQuestion holds

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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.