Evidence map›Paper›PMID 17890318›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Polylactosamine on glycoproteins influences basal levels of lymphocyte and macrophage activation.

Akira Togayachi, Yuko Kozono, Hiroyasu Ishida, Sumie Abe, Nami Suzuki, Yuki Tsunoda, Kozue Hagiwara, Atsushi Kuno, Takashi Ohkura, Nobuo Sato and 5 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

54 citing papers in PubMed, 119 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Metabolomics andCommunications biology · 2024
    Article
  6. Immunometabolism (Cobham, Surrey) · 2023
    Review
  7. Cells · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Aberrant Protein Glycosylation in Brain Cancers, with Emphasis on Glioblastoma.Advances in experimental medicine and biology · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. The Role of Glycosylation in Inflammatory Diseases.Advances in experimental medicine and biology · 2021
    Article
  16. Core-Fucosylated Tetra-AntennaryInternational journal of molecular sciences · 2019
    Article
  17. Article
  18. Article
  19. Article
  20. 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

15 authors at 1 institution in 2 countries.

Akira TogayachiResearch Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology, Central-2 OSL, 1-1-1 Umezono, Tsukuba, Ibaraki 305-8568, Japan.
Yuko Kozono
Hiroyasu Ishida
Sumie Abe
Nami Suzuki
Yuki Tsunoda
Kozue Hagiwara
Atsushi Kuno
Takashi Ohkura
Nobuo Sato
Takashi Sato
Jun Hirabayashi
Yuzuru Ikehara
Kouichi Tachibana
Hisashi Narimatsu
National Institute of Advanced Industrial Science and Technology · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

beta1,3-N-acetylglucosaminyltransferase 2 (beta3GnT2) is a polylactosamine synthase that synthesizes a backbone structure of carbohydrate structures onto glycoproteins. Here we generated beta3GnT2-deficient (beta3GnT2(-/-)) mice and showed that polylactosamine on N-glycans was markedly reduced in their immunological tissues. In WT mice, polylactosamine was present on CD28 and CD19, both known immune costimulatory molecules. However, polylactosamine levels on these molecules were reduced in beta3GnT2(-/-) mice. beta3GnT2(-/-) T cells lacking polylactosamine were more sensitive to the induction of intracellular calcium flux on stimulation with anti-CD3epsilon/CD28 and proliferated more strongly than T cells from WT mice. beta3GnT2(-/-) B cells also showed hyperproliferation on BCR stimulation. Macrophages from beta3GnT2(-/-) mice had higher cell surface CD14 levels and enhanced responses to endotoxin. These results indicate that polylactosamine on N-glycans is a putative immune regulatory factor presumably suppressing excessive responses during immune reactions.

Indexed as

Amino SugarsAnimalsAntigens, CD19CD28 AntigensLymphocyte ActivationMacrophage ActivationMiceMice, KnockoutN-AcetylglucosaminyltransferasesPlant LectinsPolysaccharidesReceptors, Antigen, T-CellSolanum lycopersicumT-LymphocytesAmino SugarsAntigens, CD19B3GNT2 protein, humanCD28 AntigensN-AcetylglucosaminyltransferasesPlant LectinspolylactosaminePolysaccharidesReceptors, Antigen, T-Cell

Identifiers

PMID17890318
PMCPMC2000437
OpenAlexW1992056223

What OpenQuestion holds

Textmetadata
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.