Evidence map›Paper›PMID 40609958›Full record

ArticleBiochimica et biophysica acta. Molecular cell research2025

GlycoRNA-L and glycoRNA-S mediate human monocyte adhesion via binding to Siglec-5.

Yong Li, Yisong Qian, Evan Huang, Zain Schwarz, Hannah Tai, Katherine Tillock, Tianhua Lei, Xiaofeng Yang, Mingui Fu

Abstract read
In one paragraph

Article in Biochimica et biophysica acta. Molecular cell research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

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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

9 authors.

Yong LiDepartment of Biomedical Science, School of Medicine, University of Missouri Kansas City, Kansas City, MO 64108, USA; Department of Anesthesiology, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi 330006, China.
Yisong QianKey Lab for Arteriosclerology of Hunan Province, International Joint Laboratory for Arteriosclerotic Disease Research of Hunan Province, Institute of Cardiovascular Disease, University of South China, Hengyang 421001, China.
Evan HuangDepartment of Biomedical Science, School of Medicine, University of Missouri Kansas City, Kansas City, MO 64108, USA.
Zain SchwarzDepartment of Biomedical Science, School of Medicine, University of Missouri Kansas City, Kansas City, MO 64108, USA.
Hannah TaiDepartment of Biomedical Science, School of Medicine, University of Missouri Kansas City, Kansas City, MO 64108, USA.
Katherine TillockDepartment of Biomedical Science, School of Medicine, University of Missouri Kansas City, Kansas City, MO 64108, USA.
Tianhua LeiDepartment of Biomedical Science, School of Medicine, University of Missouri Kansas City, Kansas City, MO 64108, USA.
Xiaofeng YangDepartment of Cardiovascular Sciences, Lemole Center for Integrated Lymphatics and Vascular Research, Lewis Katz School of Medicine at Temple University, Philadelphia, PA 19140, USA.
Mingui FuDepartment of Biomedical Science, School of Medicine, University of Missouri Kansas City, Kansas City, MO 64108, USA. Electronic address: fum@umkc.edu.

Funding

IL-35 inhibits gut microbiota-produced uremic toxin-accelerated endothelial cell activationR01HL147565 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI YANG, XIAOFENG · 2019 to 2022
$2.6M
LysoPI/GPR55 pathway promotes endothelial activation, vascular inflammation and atherosclerosisR01HL163570 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI Xiaofeng Yang · 2023 to 2026
$2.6M
NHLBI NIH HHS R01 HL147565NHLBI NIH HHS R01 HL163570
6 · The paper itself

Abstract

It was recently reported that RNAs can be glycosylated, and such glycosylated RNAs (referred to as glycoRNAs) are located on the outer cell surface. We here reported that there are two forms of glycoRNAs, named as glycoRNA-L and glycoRNA-S, robustly expressed in human monocytes. We verified that the glycoRNA-S specifically detected in human monocytes is synthesized by enzyme-catalyzed conjugation, but not artificial products of labelling probe. RNase-treatment removed both glycoRNA-L and glycoRNA-S, suggesting that they are localized on cell surface. Removing glycoRNAs significantly suppressed the interaction of human monocytes with endothelial cells, suggesting that glycoRNAs mediate human monocyte adhesion. Using flow cytometry, immunoprecipitation and northern blotting we identified Siglec-5 as the binding receptor of glycoRNAs. Siglec-5 is expressed in human endothelial cells but presented on endothelial cell surface when endothelial cells are activated. We observed that glycoRNA-L was heavily labeled with sialic acid, whereas glycoRNA-S was heavily labeled with N-acetylgalactosamine and N-acetylglucosamine. Together, these results demonstrate that two forms of glycoRNAs exist in human monocytes, which may play significant role in controlling the interaction of human monocytes and endothelial cells and contribute to the pathogenesis of inflammatory diseases.

Indexed as

Antigens, CDAntigens, Differentiation, B-LymphocyteAntigens, Differentiation, MyelomonocyticLectinsMonocytesRNA, Small NucleolarCell AdhesionEndothelial CellsGlycosylationHumansHuman Umbilical Vein Endothelial CellsProtein BindingAntigens, CDAntigens, Differentiation, B-LymphocyteAntigens, Differentiation, MyelomonocyticLectinsRNA, Small NucleolarSIGLEC5 protein, humanAdhesionGlycoRNAsMonocyteSiglec-5 and endothelial cells

Identifiers

PMID40609958
PMCPMC12281301

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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.