Macrophage cytokine response to particles and lipopolysaccharide in vitro

A U Daniels1, F H Barnes, S J Charlebois

  • 1University of Tennessee-Campbell Clinic, Department of Orthopaedic Surgery, 956 Court Avenue, Room A302, Memphis, Tennessee 38163, USA.

Insights

Adsorbed molecules on material particles significantly influence macrophage immune responses. Surface chemistry and microstructure dictate molecule concentration, impacting how particles interact with macrophage receptors.

Area of Science:

  • Biomaterials Science
  • Immunology
  • Cell Biology

Background:

  • Biologic molecules adsorbed onto particles are hypothesized to be critical in macrophage response.
  • Adsorbed endotoxins, a type of bacterial debris, are ubiquitous and bind strongly to various materials, suggesting their importance.

Purpose of the Study:

  • To investigate the in vitro macrophage response to particles with and without adsorbed lipopolysaccharide (LPS) endotoxin.
  • To determine the influence of particle material (high-density polyethylene and Co-Cr-Mo alloy) and surface contaminants on macrophage cytokine secretion.

Main Methods:

  • Utilized murine-transformed peritoneal macrophages (IC-21) in an in vitro system.
  • Measured secretions of interleukin-1 beta (IL-1β), tumor necrosis factor alpha (TNF-α), and interleukin-6 (IL-6) as indicators of macrophage response.
  • Exposed particles and experimental chambers to lipopolysaccharide (LPS) or cleaned them with ethanol and saline.

Main Results:

  • Minimal cytokine secretion was observed in response to cleaned particles and polypropylene chambers without LPS exposure.
  • High levels of cytokine secretion occurred when chambers and particles were exposed to LPS, even after rinsing.
  • Distinct cytokine secretion patterns emerged based on the presence of particles and whether they were polymer or metal.

Conclusions:

  • Adsorbed molecules on material surfaces profoundly impact macrophage responses.
  • Particle surface chemistry and microstructure influence the adsorption and configuration of molecules, thereby modulating interactions with macrophage surface receptors.

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