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Activity of polymorphonuclear leukocytes in the presence of sulfide

R Claesson1, M Granlund-Edstedt, S Persson

  • 1Department of Oral Microbiology, University of Umeå, Sweden.

Infection and Immunity
|September 1, 1989
PubMed

Insights

Hydrogen sulfide (H2S) at 1 mM did not impair polymorphonuclear leukocytes (PMN) function, suggesting PMNs can operate in infected sites with high H2S levels, aiding in its detoxification.

Area of Science:

  • Immunology
  • Biochemistry
  • Microbiology

Background:

  • Polymorphonuclear leukocytes (PMNs) are crucial immune cells involved in fighting bacterial infections.
  • Hydrogen sulfide (H2S) is a gas produced endogenously and by bacteria, with complex roles in inflammation.
  • Periodontal disease sites can exhibit elevated H2S levels, posing a challenge for PMN function.

Purpose of the Study:

  • To investigate the impact of hydrogen sulfide exposure on human PMN functions.
  • To determine if PMNs can maintain antimicrobial activity in the presence of H2S.
  • To assess the potential role of PMNs in H2S detoxification at infection sites.

Main Methods:

  • Isolation of human PMNs from blood.
  • Exposure of PMNs to varying concentrations of hydrogen sulfide (H2S).
  • Assay of respiratory burst activity, myeloperoxidase (MPO) activity, and bacterial phagocytosis/killing capacity.

Main Results:

  • 1-hour exposure to 1 mM H2S did not significantly reduce PMN myeloperoxidase activity or respiratory burst initiation.
  • The respiratory burst products rapidly oxidized H2S.
  • Phagocytosis and bacterial killing by PMNs were only slightly decreased in the presence of 1 mM H2S.
  • Myeloperoxidase activity in cell extracts was strongly inhibited by 1 µM H2S, indicating limited H2S penetration into PMNs.

Conclusions:

  • Hydrogen sulfide does not easily permeate human PMNs.
  • PMNs retain significant antimicrobial function even at high H2S concentrations.
  • PMNs may be functional in H2S-rich environments like periodontal pockets.
  • PMNs could contribute to H2S detoxification in oxygenated areas of infected sites.

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