Evidence map›Paper›PMID 10900005›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2000

Internalization of CD26 by mannose 6-phosphate/insulin-like growth factor II receptor contributes to T cell activation.

H Ikushima, Y Munakata, T Ishii, S Iwata, M Terashima, H Tanaka, S F Schlossman, C Morimoto

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

53 citing papers in PubMed, 117 citations in OpenAlex.

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  17. Dipeptidyl Peptidase-4 at the Interface Between Inflammation and Metabolism.Clinical medicine insights. Endocrinology and diabetes · 2020
    Review
  18. CD26 and Asthma: a Comprehensive Review.Clinical reviews in allergy & immunology · 2019
    Review
  19. Review
  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

8 authors at 4 institutions in 2 countries.

H IkushimaDepartment of Cancer Immunology and AIDS, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.
Y Munakata
T Ishii
S Iwata
M Terashima
H Tanaka
S F Schlossman
C Morimoto
Dana-Farber Cancer Institute · USHarvard University · USHarvard University Press · USThe University of Tokyo · JP

Funding

IMMUNOREGULATORY CIRCUITS IN MANR01AR033713 · NIAMS · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI MORIMOTO, CHIKAO · 1986 to 2002
$869k
HUMAN T-CELL SUBSETS--ISOLATION AND CHARACTERIZATIONR01AI012069 · NIAID · DANA-FARBER CANCER INSTITUTE · PI SCHLOSSMAN, STUART F · 1985 to 2001
$832k
HUMAN T-CELL SUBSETS--ISOLATION AND CHARACTERIZATIONR37AI012069 · NIAID · DANA-FARBER CANCER INSTITUTE · PI SCHLOSSMAN, STUART F · 1990 to 1996
–
NIAID NIH HHS AI12069NIAMS NIH HHS AR33713
6 · The paper itself

Abstract

CD26 is a T cell activation antigen known to bind adenosine deaminase and have dipeptidyl peptidase IV activity. Cross-linking of CD26 and CD3 with immobilized mAbs can deliver a costimulatory signal that contributes to T cell activation. Our earlier studies revealed that cross-linking of CD26 induces its internalization, the phosphorylation of a number of proteins involved in the signaling pathway, and subsequent T cell proliferation. Although these findings suggest the importance of internalization in the function of CD26, CD26 has only 6 aa residues in its cytoplasmic region with no known motif for endocytosis. In the present study, we have identified the mannose 6-phosphate/insulin-like growth factor II receptor (M6P/IGFIIR) as a binding protein for CD26 and that mannose 6-phosphate (M6P) residues in the carbohydrate moiety of CD26 are critical for this binding. Activation of peripheral blood T cells results in the mannose 6 phosphorylation of CD26. In addition, the cross-linking of CD26 with an anti-CD26 antibody induces not only capping and internalization of CD26 but also colocalization of CD26 with M6P/IGFIIR. Finally, both internalization of CD26 and the T cell proliferative response induced by CD26-mediated costimulation were inhibited by the addition of M6P, but not by glucose 6-phosphate or mannose 1-phosphate. These results indicate that internalization of CD26 after cross-linking is mediated in part by M6P/IGFIIR and that the interaction between mannose 6-phosphorylated CD26 and M6P/IGFIIR may play an important role in CD26-mediated T cell costimulatory signaling.

Indexed as

Lymphocyte ActivationCarbohydrate MetabolismCell DivisionDipeptidyl Peptidase 4HumansK562 CellsMannosephosphatesPhosphorylationReceptor, IGF Type 2T-LymphocytesDipeptidyl Peptidase 4mannose-6-phosphateMannosephosphatesReceptor, IGF Type 2

Identifiers

PMID10900005
PMCPMC26966
OpenAlexW1967273546

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.