Evidence map›Paper›PMID 2530300›Full record

ArticleThe Journal of experimental medicine1989

The specific interaction of helper T cells and antigen-presenting B cells. IV. Membrane and cytoskeletal reorganizations in the bound T cell as a function of antigen dose.

A Kupfer, S J Singer

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1989. 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
4.9field-weighted citation impact, top 4% 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, 166 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Role of Polycomb Complexes in Normal and Malignant Plasma Cells.International journal of molecular sciences · 2020
    Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. The immunological synapse.Cancer immunology research · 2014
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Modular design of immunological synapses and kinapses.Cold Spring Harbor perspectives in biology · 2009
    Review
  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

2 authors at 1 institution in 1 country.

A KupferDepartment of Biology, University of California at San Diego, La Jolla 92093.
S J Singer
University of California San Diego · US

Funding

CELL BIOLOGY OF IMMUNE INTERACTIONSR37AI023764 · NIAID · NATIONAL JEWISH HEALTH · PI KUPFER, ABRAHAM · 2000 to 2009
$4.0M
STRUCTURE OF ANTIBODY MOLECULES AND CELL MEMBRANESR01AI006659 · NIAID · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI SINGER, S J · 1985 to 1989
–
CELL BIOLOGY OF IMMUNE INTERACTIONSR01AI023764 · NIAID · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI KUPFER, ABRAHAM · 1986 to 1999
–
NIAID NIH HHS AI-06659NIAID NIH HHS AI-23764
6 · The paper itself

Abstract

We have used double-immunofluorescence labeling to determine the surface distributions of LFA-1 and CD4, and the intracellular distributions of the cytoskeletal protein talin and of the microtubule organizing center (MTOC) of cloned Th cells in 1:1 cell couples with antigen (Ag)-specific APC of the B cell type (B-APC). The Th cell was directed to a peptide fragment of the Ag OVA in the context of IAd. The B-APC was the transfected A20 B hybridoma cell A20-HL, bearing on its surface a surface Ig specific for the hapten TNP, and pulsed with different concentrations of DNP-OVA. At sufficiently high doses of DNP-OVA (greater than 100 ng/ml), in essentially all couples, LFA-1, CD4, and talin were each concentrated at the Th cell membrane where it was in contact with the B-APC, and the MTOC inside the Th cell was reoriented to face the contact region. At lower doses of DNP-OVA (between 50 and 10 ng/ml), in all couples, LFA-1 and talin were concentrated at the Th/B-APC contact region, but the extent of CD4 clustering, MTOC reorientation, and Th cell proliferation all decreased with decreasing Ag dose. With no Ag, none of these effects was observed. These and other data indicate that two distinct signals are received by the Th cell that is specifically bound to its B-APC. The first signal, at low Ag doses, stimulates a linkage of LFA-1 and talin in the Th cell, and a specific LFA-1-mediated intercellular adhesion; the second signal, at higher Ag doses, is required to induce Th cell proliferation, with which the Th-MTOC reorientation and CD4 clustering are correlated.

Indexed as

Lymphocyte CooperationAnimalsAntigen-Presenting CellsAntigens, DifferentiationAntigens, Differentiation, T-LymphocyteB-LymphocytesCell MembraneCytoskeletal ProteinsCytoskeletonDose-Response Relationship, ImmunologicFluorescent Antibody TechniqueHybridomasIntegrinsIn Vitro TechniquesLymphocyte ActivationLymphocyte Function-Associated Antigen-1Antigens, DifferentiationAntigens, Differentiation, T-LymphocyteCytoskeletal ProteinsIntegrinsLymphocyte Function-Associated Antigen-1NitrobenzenesReceptors, Antigen, T-CellReceptors, Leukocyte-AdhesionTalin

Identifiers

PMID2530300
PMCPMC2189515
OpenAlexW2160756953

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.