Evidence map›Paper›PMID 24623721›Full record

ArticleMolecular biology of the cell2014

The membrane scaffold CD82 regulates cell adhesion by altering α4 integrin stability and molecular density.

Christina M Termini, Maura L Cotter, Kristopher D Marjon, Tione Buranda, Keith A Lidke, Jennifer M Gillette

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.5field-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

48 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Review
  3. CD9-association with PIPFEBS open bio · 2025
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Tetraspanin-5-mediated MHC class I clustering is required for optimal CD8 T cell activation.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  11. Article
  12. Article
  13. Tetraspanin CD82 regulates S1PRStem cell reports · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Delivery of a model lipophilic membrane cargo to bone marrow via cell-derived microparticles.Journal of controlled release : official journal of the Controlled Release Society · 2020
    Article
  18. Article
  19. Review
  20. 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

6 authors at 1 institution in 1 country.

Christina M TerminiDepartment of Pathology, University of New Mexico Health Sciences Center, Albuquerque, NM 87131.
Maura L CotterDepartment of Pathology, University of New Mexico Health Sciences Center, Albuquerque, NM 87131.
Kristopher D MarjonDepartment of Pathology, University of New Mexico Health Sciences Center, Albuquerque, NM 87131.
Tione BurandaDepartment of Pathology, University of New Mexico Health Sciences Center, Albuquerque, NM 87131.
Keith A LidkeDepartment of Physics and Astronomy, University of New Mexico, Albuquerque, NM 87131.
Jennifer M GilletteDepartment of Pathology, University of New Mexico Health Sciences Center, Albuquerque, NM 87131 jgillette@salud.unm.edu.
University of New Mexico · US

Funding

UNM TRAININGP50GM085273 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI EDWARDS, JEREMY S · 2009 to 2018
$26.1M
NIGMS NIH HHS P50 GM085273
6 · The paper itself

Abstract

Hematopoietic stem/progenitor cell (HSPC) interactions with the bone marrow microenvironment are important for maintaining HSPC self-renewal and differentiation. In recent work, we identified the tetraspanin protein, CD82, as a regulator of HPSC adhesion and homing to the bone marrow, although the mechanism by which CD82 mediated adhesion was unclear. In the present study, we determine that CD82 expression alters cell-matrix adhesion, as well as integrin surface expression. By combining the superresolution microscopy imaging technique, direct stochastic optical reconstruction microscopy, with protein clustering algorithms, we identify a critical role for CD82 in regulating the membrane organization of α4 integrin subunits. Our data demonstrate that CD82 overexpression increases the molecular density of α4 within membrane clusters, thereby increasing cellular adhesion. Furthermore, we find that the tight packing of α4 into membrane clusters depend on CD82 palmitoylation and the presence of α4 integrin ligands. In combination, these results provide unique quantifiable evidence of CD82's contribution to the spatial arrangement of integrins within the plasma membrane and suggest that regulation of integrin density by tetraspanins is a critical component of cell adhesion.

Indexed as

Cell AdhesionCell LineCell-Matrix JunctionsCell MembraneCell MovementCellular StructuresEndocytosisFibronectinsHematopoietic Stem CellsHumansIntegrin alpha4Integrin alpha4beta1Kangai-1 ProteinLipoylationProtein TransportRNA InterferenceCD82 protein, humanFibronectinsIntegrin alpha4Integrin alpha4beta1Kangai-1 ProteinRNA, Small Interfering

Identifiers

PMID24623721
PMCPMC4019488
OpenAlexW2128661830

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.