Membrane damage and interleukin-1 production in murine macrophages exposed to listeriolysin O

Infect Immun. 1993 Apr;61(4):1334-9. doi: 10.1128/iai.61.4.1334-1339.1993.

Abstract

To obtain some insight into the interaction between listeriolysin O (LLO) and the macrophage membrane, we examined the effect of purified Listeria monocytogenes hemolysin on the viability and functions of mouse peritoneal exudate macrophages. The study showed that purified LLO impaired a variety of functions of the macrophages. First, it suppressed the luminol-dependent chemiluminescence response of macrophages. Second, it suppressed the phagocytic ingestion of opsonized sheep erythrocytes and latex beads. Third, exposure of macrophages to LLO resulted in an increase in dead cells, as determined by the trypan blue dye exclusion method. An interesting observation of this study is that the LLO-induced production of interleukin-1 from macrophages could not be blocked by preincubation with cholesterol, while the membrane-damaging ability could be blocked by cholesterol. The dissociation of the blocking effects of cholesterol suggests that the interleukin-1-inducing ability of LLO may be distinct from its membrane-damaging ability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Toxins*
  • Cell Membrane / drug effects
  • Cholesterol / pharmacology
  • Heat-Shock Proteins / antagonists & inhibitors
  • Heat-Shock Proteins / toxicity*
  • Hemolysin Proteins
  • In Vitro Techniques
  • Interleukin-1 / biosynthesis*
  • Lipopolysaccharides / pharmacology
  • Listeria monocytogenes / pathogenicity*
  • Luminescent Measurements
  • Macrophages / drug effects*
  • Mice
  • Mice, Inbred ICR
  • Peritoneal Cavity / cytology
  • Phagocytosis / drug effects

Substances

  • Bacterial Toxins
  • Heat-Shock Proteins
  • Hemolysin Proteins
  • Interleukin-1
  • Lipopolysaccharides
  • Cholesterol
  • hlyA protein, Listeria monocytogenes