Macrophages acquire neutrophil granules for antimicrobial activity against intracellular pathogens

被引:184
作者
Tan, Belinda H.
Meinken, Christoph
Bastian, Max
Bruns, Heiko
Legaspi, Annaliza
Ochoa, Maria Teresa
Krutzik, Stephan R.
Bloom, Barry R.
Ganz, Tomas
Modlin, Robert L.
Stenger, Steffen
机构
[1] Univ Erlangen Nurnberg, Inst Klin Mikrobiol Immunol & Hyg, D-91054 Erlangen, Germany
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Div Dermatol, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA
[5] Harvard Univ, Sch Publ Hlth, Off Dean, Boston, MA 02115 USA
关键词
D O I
10.4049/jimmunol.177.3.1864
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:1864 / 1871
页数:8
相关论文
共 44 条
[12]   REGULATION OF CELL-ADHESION MOLECULE EXPRESSION AND FUNCTION-ASSOCIATED WITH NEUTROPHIL APOPTOSIS [J].
DRANSFIELD, I ;
STOCKS, SC ;
HASLETT, C .
BLOOD, 1995, 85 (11) :3264-3273
[13]   Neutrophil responses to Mycobacterium tuberculosis infection in genetically susceptible and resistant mice [J].
Eruslanov, EB ;
Lyadova, IV ;
Kondratieva, TK ;
Majorov, KB ;
Scheglov, IV ;
Orlova, MO ;
Apt, AS .
INFECTION AND IMMUNITY, 2005, 73 (03) :1744-1753
[14]   Neutrophil granules and secretory vesicles in inflammation [J].
Faurschou, M ;
Borregaard, N .
MICROBES AND INFECTION, 2003, 5 (14) :1317-1327
[15]   IL-10 converts human dendritic cells into macrophage-like cells with increased antibacterial activity against virulent Mycobacterium tuberculosis [J].
Förtsch, D ;
Röllinghoff, M ;
Stenger, S .
JOURNAL OF IMMUNOLOGY, 2000, 165 (02) :978-987
[16]   Neutrophil-mediated mycobacteriocidal immunity in the lung during Mycobacterium bovis BCG infection in C57BL/6 mice [J].
Fulton, SA ;
Reba, SM ;
Martin, TD ;
Boom, WH .
INFECTION AND IMMUNITY, 2002, 70 (09) :5322-5327
[17]   DEFENSINS - NATURAL PEPTIDE ANTIBIOTICS OF HUMAN-NEUTROPHILS [J].
GANZ, T ;
SELSTED, ME ;
SZKLAREK, D ;
HARWIG, SSL ;
DAHER, K ;
BAINTON, DF ;
LEHRER, RI .
JOURNAL OF CLINICAL INVESTIGATION, 1985, 76 (04) :1427-1435
[18]   Defensins: Antimicrobial peptides of innate immunity [J].
Ganz, T .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (09) :710-720
[19]   NEUTROPHIL PSEUDOPLATELETS - THEIR DISCRIMINATION BY MYELOPEROXIDASE DEMONSTRATION [J].
HANKER, JS ;
GIAMMARA, BL .
SCIENCE, 1983, 220 (4595) :415-417
[20]  
HEIFETS L, 1980, J RETICULOENDOTH SOC, V28, P391