Evidence map›Paper›PMID 28041913›Full record

ArticleInternational journal of biological macromolecules2017

A three-dimensional in vitro model to demonstrate the haptotactic effect of monocyte chemoattractant protein-1 on atherosclerosis-associated monocyte migration.

Neda Ghousifam, Hamid Mortazavian, Rudra Bhowmick, Yolanda Vasquez, Frank D Blum, Heather Gappa-Fahlenkamp

Open access · greenAbstract read
In one paragraph

Article in International journal of biological macromolecules, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Collagen/kerateine multi-protein hydrogels as a thermally stable extracellular matrix for 3DInternational journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group · 2021
    Article
  6. Article
  7. Article
  8. Article
  9. 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.

Neda GhousifamSchool of Chemical Engineering at Oklahoma State University, Stillwater, OK, 74078, USA.
Hamid MortazavianDepartment of Chemistry at Oklahoma State University, Stillwater, OK, 74078, USA.
Rudra BhowmickSchool of Chemical Engineering at Oklahoma State University, Stillwater, OK, 74078, USA.
Yolanda VasquezDepartment of Chemistry at Oklahoma State University, Stillwater, OK, 74078, USA.
Frank D BlumDepartment of Chemistry at Oklahoma State University, Stillwater, OK, 74078, USA.
Heather Gappa-FahlenkampSchool of Chemical Engineering at Oklahoma State University, Stillwater, OK, 74078, USA. Electronic address: heather.fahlenkamp@okstate.edu.
Oklahoma State University · US

Funding

A 3D Vascular Tissue Model for Studying Cell Migration in AtherosclerosisR15EB009527 · NIBIB · OKLAHOMA STATE UNIVERSITY STILLWATER · PI FAHLENKAMP, HEATHER · 2009 to 2009
$222k
NIBIB NIH HHS R15 EB009527
6 · The paper itself

Abstract

Monocyte transendothelial migration is a multi-step process critical for the initiation and development of atherosclerosis. The chemokine monocyte chemoattractant protein-1 (MCP-1) is overexpressed during atheroma and its concentration gradients in the extracellular matrix (ECM) is critical for the transendothelial recruitment of monocytes. Based on prior observations, we hypothesize that both free and bound gradients of MCP-1 within the ECM are involved in directing monocyte migration. The interaction between a three-dimensional (3D), cell-free, collagen matrix and MCP-1; and its effect on monocyte migration was measured in this study. Our results showed such an interaction existed between MCP-1 and collagen, as 26% of the total MCP-1 added to the collagen matrix was bound to the matrix after extensive washes. We also characterized the collagen-MCP-1 interaction using biophysical techniques. The treatment of the collagen matrix with MCP-1 lead to increased monocyte migration, and this phenotype was abrogated by treating the matrix with an anti-MCP-1 antibody. Thus, our results indicate a binding interaction between MCP-1 and the collagen matrix, which could elicit a haptotactic effect on monocyte migration. A better understanding of such mechanisms controlling monocyte migration will help identify target cytokines and lead to the development of better anti-inflammatory therapeutic strategies.

Indexed as

Cell MovementModels, BiologicalCell AdhesionChemokine CCL2CollagenExtracellular MatrixHumansMonocytesPlaque, AtheroscleroticTemperatureChemokine CCL2CollagenAtherosclerosisMonocyte chemoattractant protein-1Monocyte migration

Identifiers

PMID28041913
PMCPMC5413302
OpenAlexW2565304193

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.