Evidence map›Paper›PMID 36156410›Full record

ArticleBiomaterials2022

Canonical Wnt signaling enhances pro-inflammatory response to titanium by macrophages.

Derek Avery, Lais Morandini, Luke S Sheakley, Arth H Shah, Loc Bui, Jefferson O Abaricia, Rene Olivares-Navarrete

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.4field-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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
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  9. CD4Acta biomaterialia · 2024
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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

7 authors at 1 institution in 1 country.

Derek AveryDepartment of Biomedical Engineering, College of Engineering, Virginia Commonwealth University, Richmond, VA, United States.
Lais MorandiniDepartment of Biomedical Engineering, College of Engineering, Virginia Commonwealth University, Richmond, VA, United States.
Luke S SheakleyDepartment of Biomedical Engineering, College of Engineering, Virginia Commonwealth University, Richmond, VA, United States.
Arth H ShahDepartment of Biomedical Engineering, College of Engineering, Virginia Commonwealth University, Richmond, VA, United States.
Loc BuiDepartment of Biomedical Engineering, College of Engineering, Virginia Commonwealth University, Richmond, VA, United States.
Jefferson O AbariciaDepartment of Biomedical Engineering, College of Engineering, Virginia Commonwealth University, Richmond, VA, United States.
Rene Olivares-NavarreteDepartment of Biomedical Engineering, College of Engineering, Virginia Commonwealth University, Richmond, VA, United States. Electronic address: ronavarrete@vcu.edu.
Virginia Commonwealth University · US

Funding

Role of Wnt Signaling in Macrophage Response to BiomaterialsR01DE028919 · NIDCR · VIRGINIA COMMONWEALTH UNIVERSITY · PI OLIVARES-NAVARRETE, RENE · 2019 to 2023
$1.8M
NIDCR NIH HHS R01 DE028919
6 · The paper itself

Abstract

Biomaterial characteristics like surface roughness and wettability can determine the phenotype of macrophages following implantation. We have demonstrated that inhibiting Wnt ligand secretion abolishes macrophage polarization in vitro and in vivo; however, the role of canonical Wnt signaling in macrophage activation in response to physical and chemical biomaterial cues is unknown. The aim of this study was to understand whether canonical Wnt signaling affects the response of macrophages to titanium (Ti) surface roughness or wettability in vitro and in vivo. Activating canonical Wnt signaling increased expression of toll-like receptors and interleukin receptors and secreted pro-inflammatory cytokines and reduced anti-inflammatory cytokines on Ti, regardless of surface properties. Inhibiting canonical Wnt signaling reduced pro-inflammatory cytokines on all Ti surfaces and increased anti-inflammatory cytokines on rough or rough-hydrophilic Ti. In vivo, activating canonical Wnt signaling increased total macrophages, pro-inflammatory macrophages, and T cells and decreased anti-inflammatory macrophages on both smooth and rough-hydrophilic implants. Functionally, canonical Wnt activation increases pro-inflammatory macrophage response to cell and cell-extracellular matrix lysates. These results demonstrate that activating canonical Wnt signaling primes macrophages to a pro-inflammatory phenotype that affects their response to Ti implants in vitro and in vivo.

Indexed as

TitaniumWnt Signaling PathwayAnti-Inflammatory AgentsBiocompatible MaterialsCytokinesLigandsMacrophagesSurface PropertiesAnti-Inflammatory AgentsBiocompatible MaterialsCytokinesLigandsTitaniumMacrophageMicrostructured titaniumWnt3aWnt signaling

Identifiers

PMID36156410
PMCPMC10262842
OpenAlexW4295737138

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.