Evidence map›Paper›PMID 25012074›Full record

ArticleIntegrative biology : quantitative biosciences from nano to macro2014

Effect of adhesion and chemokine presentation on T-lymphocyte haptokinesis.

George A Dominguez, Daniel A Hammer

Open access · greenAbstract read
In one paragraph

Article in Integrative biology : quantitative biosciences from nano to macro, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Morphology of Biomaterials Affect O-Glycosylation of HUVECs.Journal of functional biomaterials · 2022
    Article
  5. Integrin crosstalk allows CD4+ T lymphocytes to continue migrating in the upstream direction after flow.Integrative biology : quantitative biosciences from nano to macro · 2019
    Article
  6. Article
  7. The direction of migration of T-lymphocytes under flow depends upon which adhesion receptors are engaged.Integrative biology : quantitative biosciences from nano to macro · 2015
    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

2 authors at 2 institutions in 1 country.

George A DominguezDepartment of Bioengineering, University of Pennsylvania, 210 S. 33rd St, Philadelphia, PA 19104, USA.
Daniel A Hammer
Philadelphia University · USUniversity of Pennsylvania · US

Funding

Simulation of Lymphocyte Adhesion using Integrated Adhesive DynamicsR01AI082292 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI HAMMER, DANIEL A · 2009 to 2017
$2.8M
NIAID NIH HHS AI082292NIAID NIH HHS R01 AI082292
6 · The paper itself

Abstract

Motility is critical for the function of T-lymphocytes. Motility in T-lymphocytes is driven by the occupancy of chemokine receptors by chemokines, and modulated by adhesive interactions. However, it is not well understood how the combination of adhesion and chemokine binding affects T-lymphocyte migration. We used microcontact printing on polymeric substrates to measure how lymphocyte migration is quantitatively controlled by adhesion and chemokine ligation. Focusing only on random motion, we found that T-lymphocytes exhibit biphasic motility in response to the substrate concentration of either ICAM-1 or VCAM-1, and generally display more active motion on ICAM-1 surfaces. Furthermore, we examined how the combination of the homeostatic chemokines CCL19 and CCL21 contribute to motility. By themselves, CCL19 and CCL21, ligands for CCR7, elicit biphasic motility, but their combination synergistically increases CCR7 mediated chemokinesis on ICAM-1. By presenting CCL21 with ICAM-1 on the surface with soluble CCL19, we observed random motion that is greater than what is observed with soluble chemokines alone. These data suggest that ICAM-1 has a greater contribution to motility than VCAM-1 and that both adhesive interactions and chemokine ligation work in concert to control T-lymphocyte motility.

Indexed as

Cell AdhesionCell MovementAnimalsChemokine CCL19Chemokine CCL21ChemokinesDose-Response Relationship, DrugHomeostasisHumansImmunoglobulin GIntercellular Adhesion Molecule-1LigandsMiceProtein BindingProtein Structure, TertiaryReceptors, CCR7CCL19 protein, humanCCL21 protein, humanCCR7 protein, humanChemokine CCL19Chemokine CCL21ChemokinesImmunoglobulin GIntercellular Adhesion Molecule-1LigandsReceptors, CCR7Vascular Cell Adhesion Molecule-1

Identifiers

PMID25012074
PMCPMC4746476
OpenAlexW1968734213

What OpenQuestion holds

Textmetadata
LicenceTDM
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.