Evidence map›Paper›PMID 20932568›Full record

ArticleBiomaterials2010

Cell-cell signaling in co-cultures of macrophages and fibroblasts.

Dolly J Holt, Lisa M Chamberlain, David W Grainger

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

52 citing papers in PubMed, 133 citations in OpenAlex.

  1. Macrophage-Fibroblast Crosstalk Shapes Wound Repair Signaling In Vitro.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  2. Review
  3. Article
  4. Article
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  8. Non-small cell lung cancer organoids: Advances and challenges in current applications.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2024
    Article
  9. Article
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  14. Review
  15. Article
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  18. Huiyang Shengji Extract Improve Chronic Nonhealing Cutaneous through the TGF-Evidence-based complementary and alternative medicine : eCAM · 2021
    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

3 authors at 1 institution in 1 country.

Dolly J HoltDepartment of Bioengineering, University of Utah, Salt Lake City, UT 84112-5820, USA.
Lisa M Chamberlain
David W Grainger
University of Utah · US

Funding

Molecular Comparison of Macrophage Foreign Body ResponseR01EB000894 · NIBIB · UNIVERSITY OF UTAH · PI GRAINGER, DAVID W · 2004 to 2007
$1.1M
NIBIB NIH HHS R01 EB000894NIBIB NIH HHS R01EB00894
6 · The paper itself

Abstract

The foreign body response (FBR) comprises a general, ubiquitous host tissue-based reaction to implanted materials. In vitro cell-based models are frequently employed to study FBR mechanisms involving cell signaling responses to materials. However, these models often study only one cell type, identify only limited signals, and cannot accurately represent the complexity of in vivo inflammatory signaling. To address this issue, a cell co-culture system involving two primary effector cells of the FBR, macrophages and fibroblasts, was employed. Cell-cell signaling systems were monitored between these cell types, including long-term 1) culture of one cell type in conditioned media from the other cell type, 2) non-contacting cell co-cultures (paracrine signaling), and 3) contact co-cultures (juxtacrine signaling) of primary- and secondary-derived cells. Cell culture media and cell images were collected on Days 1, 2, 3, 7, 14, and 21 and changes in soluble protein secretion, cellular behavior, and morphology were assessed. Primary- and secondary-derived cells responded uniquely during each signaling scenario and to one another. In general higher in vitro fidelity to FBR-like responses was found in primary cell co-cultures compared to their mono-cultures and all secondary cell cultures.

Indexed as

Cell CommunicationSignal TransductionAnimalsBiological AssayCell AdhesionCell CountCell LineCell ProliferationCell ShapeCoculture TechniquesCulture Media, ConditionedCytokinesFibroblastsInflammation MediatorsKineticsLipopolysaccharidesCulture Media, ConditionedCytokinesInflammation MediatorsLipopolysaccharides

Identifiers

PMID20932568
PMCPMC2976809
OpenAlexW1965454525

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.