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Macrophages Acquire Neutrophil Granules for Antimicrobial Activity against Intracellular Pathogens
Author(s) -
Belinda H. Tan,
Christoph Meinken,
Max Bastian,
Heiko Bruns,
Annaliza J. Legaspi,
Marîa Teresa Ochoa,
Stephan R. Krutzik,
Barry R. Bloom,
Tomas Ganz,
Robert L. Modlin,
Steffen Stenger
Publication year - 2006
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.177.3.1864
Subject(s) - intracellular , intracellular parasite , phagocytosis , antimicrobial , microbiology and biotechnology , biology , innate immune system , macrophage , antimicrobial peptides , extracellular , immune system , immunology , biochemistry , in vitro
A key target of many intracellular pathogens is the macrophage. Although macrophages can generate antimicrobial activity, neutrophils have been shown to have a key role in host defense, presumably by their preformed granules containing antimicrobial agents. Yet the mechanism by which neutrophils can mediate antimicrobial activity against intracellular pathogens such as Mycobacterium tuberculosis has been a long-standing enigma. We demonstrate that apoptotic neutrophils and purified granules inhibit the growth of extracellular mycobacteria. Phagocytosis of apoptotic neutrophils by macrophages results in decreased viability of intracellular M. tuberculosis. Concomitant with uptake of apoptotic neutrophils, granule contents traffic to early endosomes, and colocalize with mycobacteria. Uptake of purified granules alone decreased growth of intracellular mycobacteria. Therefore, the transfer of antimicrobial peptides from neutrophils to macrophages provides a cooperative defense strategy between innate immune cells against intracellular pathogens and may complement other pathways that involve delivery of antimicrobial peptides to macrophages.

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