Defensin-rich granules of human neutrophils: characterization of secretory properties

被引:74
作者
Faurschou, M
Sorensen, OE
Johnsen, AH
Askaa, J
Borregaard, N
机构
[1] Natl Univ Hosp, Dept Hematol, Granulocyte Res Lab, DK-2100 OE Copenhagen, Denmark
[2] Natl Univ Hosp, Dept Clin Biochem, Rigshosp, DK-2100 OE Copenhagen, Denmark
[3] Dako AS, DK-2600 Glostrup, Denmark
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2002年 / 1591卷 / 1-3期
关键词
defensin; ELISA; subcellular fractionation; exocytosis; peroxidase-positive granule;
D O I
10.1016/S0167-4889(02)00243-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The various granule subtypes of the human neutrophil differ in propensity for exocytosis. As a rule, granules formed at late stages of myelopoiesis have a higher secretory potential than granules formed in more immature myeloid cells. Neutrophils contain four closely related alpha-defensins, which are stored in a subset of azurophil granules. These defensin-rich azurophil granules (DRG) are formed later than defensin-poor azurophil granules, near the promyelocyte/myelocyte transition. In order to characterize the secretory properties of DRG, we developed a sensitive and accurate ELISA for detection of the neutrophil alpha-defensins HNP 1-3. This allowed us to quantify the exocytosis of alpha-defensins and markers of azurophil (myeloperoxidase), specific (lactoferrin) and gelatinase (gelatinase) granules from neutrophils stimulated with different secretagogues. The release pattern of a-defensins correlated perfectly with the release of myeloperoxidase and showed no resemblance to the exocytosis of lactoferrin or gelatinase. This finding was substantiated through subcellular fractionation experiments. In conclusion, despite a distinct profile of biosynthesis, DRG are indistinguishable from defensin-poor azurophil granules with respect to exocytosis. Thus, in contrast to peroxidase-negative granules, azurophil granules display homogeneity in their availability for extracellular release. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:29 / 35
页数:7
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