Cytokine and growth factor production by monocytes/macrophages on protein preadsorbed polymers

Bonfield, T. L.; Colton, E.; Marchant, R. E.; Anderson, J. M.

doi:10.1002/jbm.820260702

Cited by 119Polymer Surface Interaction StudiesOrthopaedic implants and arthroplastyImmune cells in cancer

Cytokine and growth factor production by monocytes/macrophages on protein preadsorbed polymers

Bonfield, T. L., Colton, E., Marchant, R. E., Anderson, J. M.·1992·Journal of Biomedical Materials Research

DOI 10.1002/jbm.820260702

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Abstract

These studies evaluate the effect of biomedical polymers: Biomer, polydimethyl-siloxane (PDMS), polyethylene, expanded polytetrafluoroethylene (ePTFE), Dacron, and the control polystyrene with or without adsorbed proteins IgG, fibrinogen, and fibronectin on the ability of activated human monocytes/macrophages to produce Interleukin 1 Beta (IL-1-B), Interleukin 6 (IL-6), and Tumor Necrosis Factor Alpha (TNF-A). Monocytes/macrophages incubated on biomedical polymers with or without protein preadsorption produce variable levels of IL-1-B, IL-6, and TNF-A dependent on the polymer and adsorbed protein. IL-6 was produced in the greatest quantity and was the most influenced by protein adsorption. ePTFE and PDMS polymers were least stimulating while polystyrene was the most stimulating of monocyte activity. Adsorbed IgG consistently altered the ability of the polymers to activate monocytes/macrophages to produce cytokines. These studies provide important insight into conditions which modulate monocyte/macrophage activity in response to protein preadsorbed biomedical polymers.

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IL-6 and TNF-α in vitro macrophage secretion was differential on variant biomedical polymers.
“IL-6 and TNF-α in vitro macrophage secretion was also found to be differential on variant biomedical polymers.[105]”
From Foreign body reaction to biomaterials (2008) · cites this paper as [105]

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Authors: Bonfield, T. L., Colton, E., Marchant, R. E., & Anderson, J. M.
Affiliations: Case Western Reserve University (US)
Corresponding author: Anderson, J. M.
ORCID: Bonfield, T. L.
Anderson, J. M.
Venue: Journal of Biomedical Materials Research
Publisher: Wiley
Published: 1992-07
Volume: 26
Issue: 7
Pages: 837-850
ISSN: 0021-9304 (ISSN-L)
1097-4636
DOI: 10.1002/jbm.820260702
OpenAlex: W2150929184
Cited by: 119
References: 28
Citations by year: 2026: 2 · 2023: 1 · 2022: 1 · 2020: 1 · 2019: 2 · 2018: 1 · 2017: 2 · 2016: 2 · 2015: 1 · 2014: 3 · 2013: 1 · 2012: 9
FWCI: 4.48
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 4457 d)
Locations: Journal of Biomedical Materials Research (publishedVersion)
PubMed (publishedVersion)
Funders: National Institutes of Health (2r01hl025239-19)
National Heart, Lung, and Blood Institute (HL25239, HL40047, HL 33849)
Topics: Physical Sciences › Materials Science › Surfaces, Coatings and Films › Polymer Surface Interaction Studies
Health Sciences › Medicine › Surgery › Orthopaedic implants and arthroplasty
Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
Keywords: monocytes, macrophages, cytokine production, growth factors, protein adsorption, biomedical polymers, polydimethylsiloxane, expanded polytetrafluoroethylene, polyethylene, Dacron, polystyrene, IL-1β, interleukin-6, TNF-α, IgG, fibrinogen, fibronectin, biomaterial-immune interaction
MeSH terms: Adsorption, Adult, Cells, Cultured, Humans, Interleukin-1, Macrophages, Monocytes, Polymers, Proteins, Tumor Necrosis Factor-alpha, Interleukin-6

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Cytokine and growth factor production by monocytes/macrophages on protein preadsorbed polymers

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