Altered Proinflammatory Responses to Polyelectrolyte Multilayer Coatings Are Associated with Differences in Protein Adsorption and Wettability.


Journal

ACS applied materials & interfaces
ISSN: 1944-8252
Titre abrégé: ACS Appl Mater Interfaces
Pays: United States
ID NLM: 101504991

Informations de publication

Date de publication:
24 Nov 2021
Historique:
pubmed: 12 11 2021
medline: 11 2 2022
entrez: 11 11 2021
Statut: ppublish

Résumé

A full understanding of the relationship between surface properties, protein adsorption, and immune responses is lacking but is of great interest for the design of biomaterials with desired biological profiles. In this study, polyelectrolyte multilayer (PEM) coatings with gradient changes in surface wettability were developed to shed light on how this impacts protein adsorption and immune response in the context of material biocompatibility. The analysis of immune responses by peripheral blood mononuclear cells to PEM coatings revealed an increased expression of proinflammatory cytokines tumor necrosis factor (TNF)-α, macrophage inflammatory protein (MIP)-1β, monocyte chemoattractant protein (MCP)-1, and interleukin (IL)-6 and the surface marker CD86 in response to the most hydrophobic coating, whereas the most hydrophilic coating resulted in a comparatively mild immune response. These findings were subsequently confirmed in a cohort of 24 donors. Cytokines were produced predominantly by monocytes with a peak after 24 h. Experiments conducted in the absence of serum indicated a contributing role of the adsorbed protein layer in the observed immune response. Mass spectrometry analysis revealed distinct protein adsorption patterns, with more inflammation-related proteins (e.g., apolipoprotein A-II) present on the most hydrophobic PEM surface, while the most abundant protein on the hydrophilic PEM (apolipoprotein A-I) was related to anti-inflammatory roles. The pathway analysis revealed alterations in the mitogen-activated protein kinase (MAPK)-signaling pathway between the most hydrophilic and the most hydrophobic coating. The results show that the acute proinflammatory response to the more hydrophobic PEM surface is associated with the adsorption of inflammation-related proteins. Thus, this study provides insights into the interplay between material wettability, protein adsorption, and inflammatory response and may act as a basis for the rational design of biomaterials.

Identifiants

pubmed: 34762399
doi: 10.1021/acsami.1c16175
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Coated Materials, Biocompatible 0
Cytokines 0
Polyelectrolytes 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

55534-55549

Auteurs

Florian Billing (F)

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.

Bernadette Walter (B)

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.

Simon Fink (S)

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.

Elsa Arefaine (E)

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.

Luisa Pickarski (L)

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.

Sandra Maier (S)

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.

Robin Kretz (R)

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.

Meike Jakobi (M)

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.

Nora Feuerer (N)

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.
Department of Biomedical Engineering, Eberhard Karls University Tübingen, 72076 Tübingen, Germany.

Nicole Schneiderhan-Marra (N)

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.

Claus Burkhardt (C)

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.

Markus Templin (M)

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.

Anne Zeck (A)

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.

Rumen Krastev (R)

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.
Faculty of Applied Chemistry, Reutlingen University, 72762 Reutlingen, Germany.

Hanna Hartmann (H)

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.

Christopher Shipp (C)

NMI Natural and Medical Sciences Institute at the University of Tübingen, 72770 Reutlingen, Germany.

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Classifications MeSH