Evidence map›Paper›PMID 28340410›Full record

ArticleBiomaterials2017

Development of fusogenic glass surfaces that impart spatiotemporal control over macrophage fusion: Direct visualization of multinucleated giant cell formation.

James J Faust, Wayne Christenson, Kyle Doudrick, Robert Ros, Tatiana P Ugarova

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

11 citing papers in PubMed, 29 citations in OpenAlex.

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  11. Fabricating Optical-quality Glass Surfaces to Study Macrophage Fusion.Journal of visualized experiments : JoVE · 2018
    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

5 authors at 3 institutions in 1 country.

James J FaustSchool of Life Sciences, Arizona State University, Tempe, AZ 85287, USA; Center for Metabolic and Vascular Biology, Mayo Clinic, Scottsdale, AZ 85259, USA.
Wayne ChristensonDepartment of Physics, Arizona State University, Tempe, AZ 85287, USA; Center for Biological Physics, Arizona State University, Tempe, AZ 85287, USA.
Kyle DoudrickDepartment of Civil and Environmental Engineering and Earth Sciences, University of Notre Dame, Notre Dame, IN 46556, USA.
Robert RosDepartment of Physics, Arizona State University, Tempe, AZ 85287, USA; Center for Biological Physics, Arizona State University, Tempe, AZ 85287, USA.
Tatiana P UgarovaSchool of Life Sciences, Arizona State University, Tempe, AZ 85287, USA; Center for Metabolic and Vascular Biology, Mayo Clinic, Scottsdale, AZ 85259, USA. Electronic address: Tatiana.Ugarova@asu.edu.
Arizona State University · USMayo Clinic in Arizona · USUniversity of Notre Dame · US

Funding

The role of beta 2 integrins in macrophage fusionR01HL063199 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI Tatiana P Ugarova · 1999 to 2026
$8.6M
NHLBI NIH HHS R01 HL063199
6 · The paper itself

Abstract

Implantation of synthetic material, including vascular grafts, pacemakers, etc. results in the foreign body reaction and the formation of multinucleated giant cells (MGCs) at the exterior surface of the implant. Despite the long-standing premise that fusion of mononucleated macrophages results in the formation of MGCs, to date, no published study has shown fusion in context with living specimens. This is due to the fact that optical-quality glass, which is required for the majority of live imaging techniques, does not promote macrophage fusion. Consequently, the morphological changes that macrophages undergo during fusion as well as the mechanisms that govern this process remain ill-defined. In this study, we serendipitously identified a highly fusogenic glass surface and discovered that the capacity to promote fusion was due to oleamide contamination. When adsorbed on glass, oleamide and other molecules that contain long-chain hydrocarbons promoted high levels of macrophage fusion. Adhesion, an essential step for macrophage fusion, was apparently mediated by Mac-1 integrin (CD11b/CD18, α

Indexed as

AdsorptionAnimalsCell AdhesionCell FusionGiant CellsGlassHEK293 CellsHumansMacrophage-1 AntigenMacrophagesMice, Inbred C57BLOleic AcidsOptical PhenomenaSurface PropertiesTime FactorsMacrophage-1 AntigenOleic AcidsoleylamideForeign body reactionLive imagingMac-1 integrinMacrophage fusionMicroscopyMultinucleated giant cells

Identifiers

PMID28340410
PMCPMC5540443
OpenAlexW2592784119

What OpenQuestion holds

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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.