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Human polymorphonuclear leukocytes lack detectable nitric oxide synthase activity

L Yan1, R W Vandivier, A F Suffredini

  • 1Critical Care Medicine Department, Warren Grant Magnuson Clinical Center, National Institutes of Health, Bethesda, MD 20892.

Journal of Immunology (Baltimore, Md. : 1950)
|August 15, 1994
PubMed
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Human polymorphonuclear leukocytes (PMNs) do not exhibit nitric oxide synthase (NOS) activity. Studies comparing PMNs and human aortic endothelial cells (HAECs) found no inducible NOS activity in PMNs.

Area of Science:

  • Immunology
  • Cell Biology
  • Biochemistry

Background:

  • Nitric oxide (NO) is crucial for regulating polymorphonuclear leukocyte (PMN) functions.
  • The presence and activity of nitric oxide synthase (NOS) in human PMNs remain a subject of scientific debate.

Purpose of the Study:

  • To investigate and clarify the existence of nitric oxide synthase (NOS) activity in human polymorphonuclear leukocytes (PMNs).
  • To compare NOS activity in human PMNs with that of human aortic endothelial cells (HAECs).

Main Methods:

  • Quantified NOS activity by measuring the conversion of L-arginine to L-citrulline.
  • Utilized the NOS inhibitor N omega-amino-L-arginine (L-NAA) to assess specificity.
  • Assessed NOS induction in PMNs using various inflammatory stimuli (LPS, IL-1 beta, IFN-gamma, TNF-alpha).

Related Experiment Videos

  • Compared whole-cell and fractionated cell assays in PMNs and HAECs.
  • Measured nitrite and nitrate release from PMNs.
  • Main Results:

    • L-arginine to L-citrulline conversion, a marker of NOS activity, was significantly lower in human PMNs compared to HAECs.
    • NOS activity in PMNs was not inducible by inflammatory cytokines or LPS administration.
    • L-NAA did not inhibit L-arginine conversion in PMNs, and nitrite/nitrate release was minimal.
    • Calmodulin inhibition did not affect PMN L-arginine conversion.

    Conclusions:

    • Human polymorphonuclear leukocytes (PMNs) do not express significant nitric oxide synthase (NOS) activity.
    • These findings resolve controversy regarding NOS expression in human PMNs, differentiating them from endothelial cells.