MR detection of LPS-induced neutrophil activation using mannan-coated superparamagnetic iron oxide nanoparticles

Han Shanhua1, Han Huijing, Myeong Ju Moon

  • 1Department of Radiology, Chonnam National University Hwasun Hospital, Chonnam National University Medical School, Gwangju, 501-757, South Korea.

Abstract

Insights

Mannan-coated superparamagnetic iron oxide nanoparticles (M-SPION) effectively labeled lipopolysaccharide (LPS)-induced neutrophils, showing increased iron uptake. This technique shows promise for diagnosing LPS-induced neutrophils using MR imaging.

Area of Science:

  • Biomedical Engineering
  • Nanotechnology
  • Immunology

Background:

  • Neutrophils play a crucial role in the innate immune response.
  • Lipopolysaccharide (LPS) induces neutrophil activation and phagocytic activity.
  • Superparamagnetic iron oxide nanoparticles (SPIONs) offer potential for diagnostic imaging.

Purpose of the Study:

  • To investigate the phagocytic activity of LPS-induced neutrophils labeled with mannan-coated SPIONs (M-SPIONs).
  • To evaluate M-SPIONs as a tool for labeling and detecting LPS-induced neutrophils in vitro.

Main Methods:

  • Human neutrophils were divided into control and LPS-induced groups.
  • Neutrophils were labeled with M-SPIONs and dextran-coated SPIONs (D-SPIONs).
  • Magnetic resonance imaging (MRI) signal intensity and intracellular iron uptake (Prussian blue staining) were assessed.

Main Results:

  • M-SPION labeling resulted in significantly lower signal intensity in LPS-induced neutrophils compared to controls.
  • Intracellular iron uptake was markedly demonstrated in LPS-induced neutrophils labeled with M-SPIONs.
  • M-SPIONs proved more effective than D-SPIONs for in vitro neutrophil labeling.

Conclusions:

  • In vitro labeling of LPS-induced neutrophils with M-SPIONs is feasible.
  • This M-SPION labeling technique shows potential for developing a diagnostic method for LPS-induced neutrophils using MR imaging.

Related Concept Videos