Liposome-encapsulated hemoglobin modulates lipopolysaccharide-induced tumor necrosis factor-α production in mice

Alan S. Rudolph, Richard Cliff, Victoria Kwasiborski, Lewis Neville, Fizan Abdullah, Reuven Rabinovici

Research output: Contribution to journalArticle

Abstract

Objective: To investigate the effect of liposome-encapsulated hemoglobin, an experimental blood substitute, on the function of the mononuclear phagocytic system in normovolemic mice, in ex vivo murine splenocytes and in a transformed murine monocytic cell line, RAW 264.7. Design: Prospective, randomized trial. Setting: Center for Biomolecular Science and Engineering, Naval Research Laboratory, and the Thomas Jefferson University. Subjects: Female Balb/c mice (n = 27). Interventions: Mice were injected into the tall vein with liposome-encapsulated hemoglobin or liposome vehicle and were killed at varying time points for blood sampling and splenocyte isolation and culture. Measurements and Main Results: Injection of liposome-encapsulated hemoglobin in mice (2.2 g of lipid/kg and 0.56 g of hemoglobin/kg, n = 9) did not increase serum tumor necrosis factor (TNF)-α concentrations at 2, 8, 15, and 24 hrs after administration. In the ex vivo procedure, lipopolysaccharide (1 μg/mL)-induced TNF-α production by splenocytes from mice injected with liposome-encapsulated hemoglobin was attenuated at 2 end 4 hrs (73%, p = .002 at 2 hrs), compared with TNF-α production by splenocytes from sham animals challenged with the same concentration of lipopolysaccharide. In the in vitro procedure, simultaneous exposure of liposome-encapsulated hemoglobin (0.88 to 8.8 mg/mL) and lipopolysaccharide (0.125 to 1 μg/mL) to the murine-derived, peritoneal monocytic RAW 264.7 cell line showed significantly reduced TNF-α peptide, but not messenger RNA, 1 to 4 hrs after exposure as compared with cells challenged with lipopolysaccharide alone. This effect correlated with the rapid phagocytosis (1 hr to 4 hrs) of liposome-encapsulated hemoglobin by RAW 264.7 cells. Phagocytic activity in RAW 264.7 cells exposed to both liposome- encapsulated hemoglobin and lipopolysaccharide showed reduced uptake compared with uptake of liposome-encapsulated hemoglobin. The liposome-induced reduction in TNF-α peptide production elicited by lipopolysaccharide was countered by extending the time period to an overnight delay between liposome-encapsulated hemoglobin exposure and lipopolysaccharide challenge. Liposome-encapsulated hemoglobin incubated with lipopolysaccharide in vitro, and subsequently washed to remove free lipopolysaccharide, stimulated TNF-α expression by RAW 264.7 cells. Incubation with liposome-encapsulated hemoglobin alone did not evoke TNF-α production in these cells. Conclusions: These data suggest that liposome-encapsulated hemoglobin modulates the response of the mononuclear phagocyte system to endotoxin, possibly through binding of lipopolysaccharide, presentation to macrophages with subsequent phagocytosis, and modulation of cytokine response by a posttranscriptional mechanism. This effect is attenuated by extending the period between exposure to liposome-encapsulated hemoglobin and endotoxin. The clinical relevance of these findings awaits further investigation.

Original languageEnglish (US)
Pages (from-to)460-468
Number of pages9
JournalCritical Care Medicine
Volume25
Issue number3
DOIs
StatePublished - Mar 1997
Externally publishedYes

Keywords

  • blood substitute
  • cytokines
  • endotoxin
  • hemoglobin
  • liposomes
  • mononuclear phagocytic system
  • splenocytes
  • transcription

ASJC Scopus subject areas

  • Critical Care and Intensive Care Medicine

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