Myeloperoxidase Stimulates Neutrophil Degranulation


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Myeloperoxidase, heme enzyme of azurophilic granules in neutrophils, is released into the extracellular space in the inflammation foci. In neutrophils, it stimulates a dose-dependent release of lactoferrin (a protein of specific granules), lysozyme (a protein of specific and azurophilic granules), and elastase (a protein of azurophilic granules). 4-Aminobenzoic acid hydrazide, a potent inhibitor of peroxidase activity of myeloperoxidase, produced no effect on neutrophil degranulation. Using signal transduction inhibitors (genistein, methoxyverapamil, wortmannin, and NiCl2), we demonstrated that myeloperoxidase-induced degranulation of neutrophils resulted from enzyme interaction with the plasma membrane and depends on activation of tyrosine kinases, phosphatidylinositol 3-kinases (PI3K), and calcium signaling. Myeloperoxidase modified by oxidative/halogenation stress (chlorinated and monomeric forms of the enzyme) lost the potency to activate neutrophil degranulation.

作者简介

D. Grigorieva

Physics Faculty, Belarusian State University

Email: o-panas@mail.ru
白俄罗斯, Minsk

I. Gorudko

Physics Faculty, Belarusian State University

Email: o-panas@mail.ru
白俄罗斯, Minsk

A. Sokolov

Institute of Experimental Medicine; Scientific Research Institute of Physical-Chemical Medicine, Russian Federal Medical-Biological Agency

Email: o-panas@mail.ru
俄罗斯联邦, St. Petersburg; Moscow

V. Kostevich

Institute of Experimental Medicine; Scientific Research Institute of Physical-Chemical Medicine, Russian Federal Medical-Biological Agency

Email: o-panas@mail.ru
俄罗斯联邦, St. Petersburg; Moscow

V. Vasilyev

Institute of Experimental Medicine

Email: o-panas@mail.ru
俄罗斯联邦, St. Petersburg

S. Cherenkevich

Physics Faculty, Belarusian State University

Email: o-panas@mail.ru
白俄罗斯, Minsk

O. Panasenko

Scientific Research Institute of Physical-Chemical Medicine, Russian Federal Medical-Biological Agency

编辑信件的主要联系方式.
Email: o-panas@mail.ru
俄罗斯联邦, Moscow

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