Mannan decelerates the clearance of human red blood cells in SCID mouse

Immunopharmacology. 1998 Jan;38(3):223-8. doi: 10.1016/s0162-3109(97)00054-4.

Abstract

Mannans and its related compounds decelerated human (Hu) red blood cell (RBC)-clearance in severe combined immunodeficiency (SCID) mice by inhibiting erythro-phagocytosis of macrophages. Chimeric SCID mice for Hu-RBC which are generated by repeated transfusions with mature Hu-RBCs are described recently as a model for Plasmodium falciparum infection, though the Hu-RBC clearance in the mice at present is very rapid and the parasitemia in the mice is only erratic. Here, we aimed to study the method to decelerate Hu-RBC clearance in SCID mice, to establish a suitable mouse model for malaria parasites. Yeast and Candida mannans as well as lactoferrin, a glycoprotein containing both oligomannoside- and N-acetyllactosamine-type glycans, decelerated Hu-RBC clearance, but instead other saccharides such as carboxymethyl chitin, N-acetylglucosamine, and D-glucose did not. Yeast mannan and lactoferrin interfered significantly with in vitro Hu-RBC-phagocytosis which was also inhibited by mannopentaose and mannotoriose. D-mannose exhibited a moderate inhibitory activity. N-acetyl-D-glucosamine, however, showed only a slight inhibitory activity, but D-glucose had no inhibitory activity on Hu-RBC phagocytosis. These results may postulate that Hu-RBC clearance in SCID mouse might be mediated by receptor-ligand binding by a macrophage lectin like receptor with mannose specificity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylglucosamine / pharmacology
  • Animals
  • Candida / metabolism
  • Chimera
  • Chitin / analogs & derivatives
  • Chitin / pharmacology
  • Disease Models, Animal
  • Erythrocyte Transfusion
  • Erythrocytes*
  • Female
  • Glucose / pharmacology
  • Humans
  • Lactoferrin / pharmacology
  • Macrophages / drug effects*
  • Macrophages / physiology
  • Malaria, Falciparum / blood
  • Male
  • Mannans / pharmacology*
  • Mice
  • Mice, SCID
  • Phagocytosis / drug effects*
  • Receptors, Mitogen / drug effects
  • Yeasts / metabolism

Substances

  • Mannans
  • Receptors, Mitogen
  • Chitin
  • O-(carboxymethyl)chitin
  • Lactoferrin
  • Glucose
  • Acetylglucosamine