Induction of caspase- and reactive oxygen species-independent phosphatidylserine externalization in primary human neutrophils: role in macrophage recognition and engulfment

被引:36
作者
Jitkaew, Siriporn [2 ,3 ]
Witasp, Erika
Zhang, Shouting
Kagan, Valerian E. [4 ]
Fadeel, Bengt [1 ]
机构
[1] Karolinska Inst, Inst Environm Med, Div Biochem Toxicol, Cell Death Res Grp, S-17177 Stockholm, Sweden
[2] Mahidol Univ, Siriraj Hosp, Fac Med, Dept Biochem, Bangkok 10700, Thailand
[3] Mahidol Univ, Inst Sci & Technol Res & Dev, Thalassemia Res Ctr, Nakhon Pathom, Thailand
[4] Univ Pittsburgh, Dept Environm & Occupat Hlth, Pittsburgh, PA USA
基金
瑞典研究理事会; 美国国家卫生研究院;
关键词
annexin I; inflammation; phagocytosis; LEUKEMIA CELL-LINE; APOPTOTIC CELLS; SURFACE EXPOSURE; PHAGOCYTOSIS; CLEARANCE; IDENTIFICATION; INFLAMMATION; INVOLVEMENT; MECHANISMS; LEUKOCYTES;
D O I
10.1189/jlb.0408232
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Macrophage recognition and disposal of neutrophils are important steps in the resolution of inflammation. Externalization of phosphatidylserine (PS) on the cell surface serves as a common recognition signal for macrophages and is associated with the apoptosis program in neutrophils. Here, we report that macrophage-differentiated PLB-985 cells induce rapid, caspase-independent PS externalization in human neutrophils. A similar degree of PS externalization was seen when neutrophils were cocultured with gp91(phox)-deficient PLB-985 macrophages, thus demonstrating that macrophage-induced PS externalization was NADPH oxidase-independent. Macrophage-induced PS externalization required cell-to-cell contact and kinase activation and was shown to correlate with neutrophil degranulation. Of note, the degree of engulfment of such PS-positive neutrophils by activated human monocyte-derived macrophages was considerably lower than for neutrophils undergoing constitutive apoptosis, indicating that PS externalization alone is not sufficient for macrophage disposal of neutrophils. However, addition of recombinant milk fat globule epidermal growth factor 8, a PS-binding protein, restored engulfment of the macrophage-cocultured target cells. Finally, neutrophils undergoing spontaneous apoptosis but not macrophage-cocultured neutrophils displayed surface expression and release of annexin I, and the addition of N-t-Boc-Phe-D-Leu-Phe-D-Leu-Phe (Boc1), a formyl peptide receptor/lipoxin receptor antagonist, suppressed clearance of apoptotic neutrophils. Conditioned medium from apoptotic neutrophils also promoted the engulfment of macrophage-cocultured neutrophils, and Boc1 blocked this process. Taken together, these studies highlight a novel pathway of PS externalization in primary human neutrophils and also provide evidence for an auxiliary function of annexin I in macrophage clearance of neutrophils. J. Leukoc. Biol. 85: 427-437; 2009.
引用
收藏
页码:427 / 437
页数:11
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