Abstract
Phenylhydrazine (Phz) is a powerful hemolytic agent which has several effects on both normal and G6PD déficient red blood cells (RBCs). We have studied the mechanism of removal of Phz-damaged human RBCs by murine macrophages. Phagocytosis of Phz-treated RBCs was found to be 50 RBCs/100 mac as compared to 2 RBCs/100 mac of the controls. EGTA and sodium azide inhibited the phagocytosis, indicating a requirement for both calcium ions and energy. Incubation of macrophages with sugars such as d-galactose or d-mannose reduced phagocytosis of Phz-treated RBCs by up to 60%, indicating the involvement of a macrophage lectin-like receptor in the recognition of Phz-treated RBCs. The presence of serum in the phagocytosis assay did not affect either phagocytosis of Phz-treated RBCs or inhibition by sugars. β-Galactosidase, but not neuraminidase, treatment of RBCs caused a significant inhibition in phagocytosis of Phz-treated RBCs. These results suggest that galactosyl residues are exposed on RBC membrane during oxidation, probably not as a result of desialization. We conclude that Phz-treated RBCs are detected as damaged cells mainly due to sugar changes on their membrane, which are directly recognized by lectin-like receptors on the macrophages.
| Original language | English |
|---|---|
| Pages (from-to) | 775-780 |
| Number of pages | 6 |
| Journal | Biochemical Pharmacology |
| Volume | 39 |
| Issue number | 4 |
| DOIs | |
| State | Published - 15 Feb 1990 |
ASJC Scopus subject areas
- Biochemistry
- Pharmacology
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