Evidence map›Paper›PMID 22084235›Full record

ArticleThe Journal of biological chemistry2012

Core fucosylation of μ heavy chains regulates assembly and intracellular signaling of precursor B cell receptors.

Wenzhe Li, Qingping Liu, Yue Pang, Jinhua Jin, Huiguo Wang, Hongyu Cao, Zhi Li, Xu Wang, Biao Ma, Yan Chi and 4 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  6. Review
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  8. Review
  9. Review
  10. Review
  11. The role ofFrontiers in immunology · 2023
    Review
  12. Synthetic nanobodies as tools to distinguish IgG Fc glycoforms.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Review
  14. Review
  15. The Role of Glycosylation in Inflammatory Diseases.Advances in experimental medicine and biology · 2021
    Article
  16. Article
  17. Journal of immunology (Baltimore, Md. : 1950) · 2020
    Article
  18. Article
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

14 authors at 6 institutions in 2 countries.

Wenzhe LiInstitute of Immunology, College of Life Science and Technology, Dalian University, 10-Xuefu Avenue, Dalian Economical and Technological Development Zone, Liaoning 116622, China. liwenzhe46@hotmail.com
Qingping Liu
Yue Pang
Jinhua Jin
Huiguo Wang
Hongyu Cao
Zhi Li
Xu Wang
Biao Ma
Yan Chi
Renjun Wang
Akihiro Kondo
Jianguo Gu
Naoyuki Taniguchi
Dalian University of Technology · CNDalian University · CNDalian Municipal Central Hospital · CNRIKEN Advanced Science Institute · JPThe University of Osaka · JPTohoku Medical and Pharmaceutical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

α1,6-Fucosyltransferase (Fut8) knock-out (Fut8(-/-)) mice showed an abnormality in pre-B cell generation. Membrane assembly of pre-BCR is a crucial checkpoint for pre-B cell differentiation and proliferation in both humans and mice. The assembly of pre-BCR on the cell surface was substantially blocked in the Fut8-knockdown pre-B cell line, 70Z/3-KD cells, and then completely restored by re-introduction of the Fut8 gene to 70Z/3-KD (70Z/3-KD-re) cells. Moreover, loss of α1,6-fucosylation (also called core fucosylation) of μHC was associated with the suppression of the interaction between μHC and λ5. In contrast to Fut8(+/+) CD19(+)CD43(-) cells, the subpopulation expressing the μHC·λ5 complex in the Fut8(-/-) CD19(+)CD43(-) cell fraction was decreased. The pre-BCR-mediated tyrosine phosphorylation of CD79a and activation of Btk were attenuated in Fut8-KD cells, and restored in 70Z/3-KD-re cells. The frequency of CD19(low)CD43(-) cells (pre-B cell enriched fraction) was also reduced in Fut8(-/-) bone marrow cells, and then the levels of IgM, IgG, and IgA of 12-week-old Fut8(-/-) mice sera were significantly lower than those of Fut8(+/+) mice. Our results suggest that the core fucosylation of μHC mediates the assembly of pre-BCR to regulate pre-BCR intracellular signaling and pre-B cell proliferation.

Indexed as

AnimalsFucoseFucosyltransferasesGlycosylationImmunoglobulin AImmunoglobulin GImmunoglobulin lambda-ChainsImmunoglobulin MImmunoglobulin mu-ChainsMiceMice, KnockoutPrecursor Cells, B-LymphoidReceptors, Antigen, B-CellSignal TransductionFucoseFucosyltransferasesGlycoprotein 6-alpha-L-fucosyltransferaseImmunoglobulin AImmunoglobulin GImmunoglobulin lambda-ChainsImmunoglobulin MImmunoglobulin mu-ChainsReceptors, Antigen, B-Cell

Identifiers

PMID22084235
PMCPMC3268410
OpenAlexW2059027548

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.