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Phagocytosis of particulate nickel compounds by rat peritoneal macrophages in vitro

Carcinogenesis
|January 1, 1982
PubMed

Insights

Phagocytic activity of nickel compounds by rat macrophages varied greatly, with nickel oxide (NiO) showing the highest index and amorphous nickel sulfide (NiS) the lowest. Phagocytosis correlated with dissolution rates, except for nickel subsulfide (α Ni3S2).

Area of Science:

  • Toxicology
  • Cell Biology
  • Materials Science

Background:

  • Macrophages play a crucial role in the innate immune system, engulfing foreign particles.
  • Nickel compounds are widely used industrially, necessitating an understanding of their biological interactions.
  • The phagocytic uptake of nickel compounds by macrophages is a key factor in their toxicological profile.

Purpose of the Study:

  • To evaluate and rank the in vitro phagocytic indices of 17 different nickel compounds using rat peritoneal macrophages.
  • To investigate the correlation between the phagocytic activity of nickel compounds and their dissolution rates in rat serum.
  • To explore potential correlations between phagocytic indices and carcinogenicity data.

Main Methods:

  • In vitro exposure of rat peritoneal macrophages to 17 nickel compounds at a concentration of 10 μg/ml for 1 hour at 37°C.
  • Measurement of phagocytic indices, defined as the percentage of macrophages engulfing particles (1.5 μm median diameter).
  • Comparison of phagocytic indices with dissolution half-times in rat serum and preliminary carcinogenicity data.

Main Results:

  • Phagocytic indices ranged from 69% for NiO to 3% for amorphous NiS, with a clear ranking of compounds observed.
  • A significant rank-correlation (P < 0.03) was found between phagocytic indices and dissolution half-times in rat serum.
  • Nickel subsulfide (α Ni3S2) was highly phagocytized despite having a short dissolution half-time, indicating a complex interaction.

Conclusions:

  • The phagocytic uptake of nickel compounds by macrophages is highly variable and depends on the specific compound.
  • Dissolution rate is a significant, but not the sole, determinant of nickel compound phagocytosis.
  • Further research is needed to fully elucidate the relationship between nickel compound phagocytosis, dissolution, and long-term toxicity, including carcinogenicity.

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