Evidence map›Paper›PMID 34484231›Full record

ArticleFrontiers in immunology2021

Precision N-Glycoproteomic Profiling of Murine Peritoneal Macrophages After Different Stimulations.

Lujie Yang, Tianqi Gong, Huali Shen, Jiangnan Pei, Lei Zhang, Quanqing Zhang, Yuanyu Huang, Zuojian Hu, Ziyue Pan, Pengyuan Yang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Modulation of Macrophages TLR4-Mediated Transcriptional Response byInternational journal of molecular sciences · 2025
    Article
  2. Article
  3. Impaired bisecting GlcNAc reprogrammed M1 polarization of macrophage.Cell communication and signaling : CCS · 2024
    Article
  4. Review
  5. Review
  6. 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

12 authors at 6 institutions in 2 countries.

Lujie YangInstitutes of Biomedical Sciences & Shanghai Stomatological Hospital, Fudan University, Shanghai, China.
Tianqi GongInstitutes of Biomedical Sciences & Shanghai Stomatological Hospital, Fudan University, Shanghai, China.
Huali ShenInstitutes of Biomedical Sciences & Shanghai Stomatological Hospital, Fudan University, Shanghai, China.
Jiangnan PeiObestetics & Gynecology Hospital, Fudan University, Shanghai, China.
Lei ZhangInstitutes of Biomedical Sciences & Shanghai Stomatological Hospital, Fudan University, Shanghai, China.
Quanqing ZhangDepartment of Chemistry and Environmental Toxicology Graduate Program, University of California, Riverside, CA, United States.
Yuanyu HuangInstitutes of Biomedical Sciences & Shanghai Stomatological Hospital, Fudan University, Shanghai, China.
Zuojian HuDepartment of Clinical Laboratory, First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Ziyue PanInstitutes of Biomedical Sciences & Shanghai Stomatological Hospital, Fudan University, Shanghai, China.
Pengyuan YangInstitutes of Biomedical Sciences & Shanghai Stomatological Hospital, Fudan University, Shanghai, China.
Ling LinXiamen Cardiovascular Hospital, Xiamen University, Xiamen, China.
Hongxiu YuInstitutes of Biomedical Sciences & Shanghai Stomatological Hospital, Fudan University, Shanghai, China.
Shanghai Stomatological Hospital · CNFudan University · CNFirst Affiliated Hospital of GuangXi Medical University · CNFirst Affiliated Hospital of Xiamen University · CNObstetrics and Gynecology Hospital of Fudan University · CNUniversity of California, Riverside · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophages are important immune cells that participate in both innate and adaptive immune responses, such as phagocytosis, recognition of molecular patterns, and activation of the immune response. In this study, murine peritoneal macrophages were isolated and then activated by LPS, HSV and VSV. Integrative proteomic and precision N-glycoproteomic profiling were conducted to assess the underlying macrophage activation. We identified a total of 587 glycoproteins, including 1239 glycopeptides, 526 monosaccharide components, and 8326 intact glycopeptides in glycoproteomics, as well as a total of 4496 proteins identified in proteomic analysis. These glycoproteins are widely involved in important biological processes, such as antigen presentation, cytokine production and glycosylation progression. Under the stimulation of the different pathogens, glycoproteins showed a dramatic change. We found that receptors in the Toll-like receptor pathway, such as Tlr2 and CD14, were increased under LPS and HSV stimulation. Glycosylation of those proteins was proven to influence their subcellular locations.

Indexed as

ProteomeProteomicsAnimalsChromatography, High Pressure LiquidComputational BiologyCytokinesGene Expression RegulationGene Regulatory NetworksGlycoproteinsMacrophage ActivationMacrophages, PeritonealMiceModels, BiologicalNIH 3T3 CellsRAW 264.7 CellsCytokinesGlycoproteinsProteomeglycoproteomicsinflammatory responsemacrophageN-glycosylationToll-like receptors

Identifiers

PMID34484231
PMCPMC8416091
OpenAlexW3196178904

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.